AU2001291013A1 - Pyrazole compounds useful as protein kinase inhibitors - Google Patents

Pyrazole compounds useful as protein kinase inhibitors

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AU2001291013A1
AU2001291013A1 AU2001291013A AU9101301A AU2001291013A1 AU 2001291013 A1 AU2001291013 A1 AU 2001291013A1 AU 2001291013 A AU2001291013 A AU 2001291013A AU 9101301 A AU9101301 A AU 9101301A AU 2001291013 A1 AU2001291013 A1 AU 2001291013A1
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David Bebbington
Robert Davies
Cornelia Forester
David Kay
Ronald Knegtel
Pan Li
Albert Pierce
Marion Wannamaker
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Vertex Pharmaceuticals Inc
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Vertex Pharmaceuticals Inc
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Application filed by Vertex Pharmaceuticals Inc filed Critical Vertex Pharmaceuticals Inc
Publication of AU2001291013A1 publication Critical patent/AU2001291013A1/en
Priority to AU2006201264A priority Critical patent/AU2006201264A1/en
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Description

PYRAZOLE COMPOUNDS USEFUL AS PROTEIN KINASE INHIBITORS
CROSS REFERENCE TO RELATED APPLICATIONS This application claims priority to US Provisional Patent Application 60/232,795 filed September 15, 2000, US Provisional Patent Application 60/257,887 filed December 21, 2000 and US Provisional Patent Application 60/286,949 filed April 27, 2001, the contents of which are incorporated herein by reference .
FIELD OF THE INVENTION The present invention is in the field of medicinal chemistry and relates to compounds that are protein kinase inhibitors, compositions containing such compounds and methods of use. More particularly, this invention relates to compounds that are inhibitors of GSK-3 and Aurora-2 protein kinases. The invention also relates to methods of treating diseases associated with these protein kinases, such as diabetes, cancer and Alzheimer's disease.
BACKGROUND OF THE INVENTION The search for new therapeutic agents has been greatly aided in recent years by better understanding of the structure of enzymes and other biomolecules associated with target diseases. One important class of enzymes that has been the subject of extensive study is the protein kinases .
Protein kinases mediate intracellular signal transduction. They do this by effecting a phosphoryl transfer from a nucleoside triphosphate to a protein acceptor that is involved in a signaling pathway. There are a number of kinases and pathways through which extracellular and other stimuli cause a variety of cellular responses to occur inside the cell. Examples of such stimuli include environmental and chemical stress signals (e.g. osmotic shock, heat shock, ultraviolet radiation, bacterial endotoxin, H202) , cytokines (e.g. interleukin-1 (IL-1) and tumor necrosis factor α (TNF- α) ) , and growth factors (e.g. granulocyte' macrophage- colony-stimulating factor (GM-CSF) , and fibroblast growth factor (FGF) . An extracellular stimulus may effect one or more cellular responses related to cell growth, migration, di ferentiation, secretion of hormones, activation of transcription factors, muscle contraction, glucose metabolism, control of protein synthesis and regulation of cell cycle.
Many diseases are associated with abnormal cellular responses triggered by protein kinase-mediated events. These diseases include autoimmune diseases, inflammatory diseases, neurological and neurodegenerative diseases, cancer, cardiovascular diseases, allergies and asthma, Alzheimer's disease or hormone-related diseases. Accordingly, there has been a substantial effort in medicinal chemistry to find protein kinase inhibitors that are effective as therapeutic agents . Aurora-2 is a serine/threonine protein kinase that has been implicated in human cancer, such as colon, breast and other solid tumors. This kinase is believed to be involved in protein phosphorylation events that regulate the cell cycle. Specifically, Aurora-2 may play a role in controlling the accurate segregation of chromosomes during mitosis . Misregulation of the cell cycle can lead to cellular proliferation and other abnormalities. In human colon cancer tissue, the aurora- 2 protein has been found to be overexpressed. See •Bischoff et al., EMBO J. , 1998, 17, 3052-3065; Schumacher et al., J". Cell Biol . , 1998', 143, 1635-1646; Kimura et al., J. Biol . Chem. , 1997, 272, 13766-13771. Glycogen synthase kinase-3 (GSK-3) is a serine/threonine protein kinase comprised of α and β isoforms that are each encoded by distinct genes [Coghlan et al., Chemistry & Biology, 7, 793-803 (2000); Kim and Kimmel, Curr. Opinion Genetics Dev. , 10, 508-514 (2000)]. GSK-3 has been implicated in various diseases including diabetes, Alzheimer's disease, CNS disorders such as manic depressive disorder and neurodegenerative diseases, and cardiomyocete hypertrophy [WO 99/65897; WO 00/38675; and Haq et al . , J". Cell Biol . (2000) 151, 117]. These diseases may be caused by, or result in, the abnormal operation of certain cell signaling pathways in which GSK-3 plays a role. GSK-3 has been found to phosphorylate and modulate the activity of a number of regulatory proteins . These proteins include glycogen synthase which is the rate limiting enzyme necessary for glycogen synthesis, the icrotubule associated protein Tau, the gene transcription factor β-catenin, the translation initiation factor elF2B, as well as ATP citrate lyase, axin, .heat shock factor-1, c-Jun, c-Myc, c-Myb, CREB, and CEPBα. These diverse protein targets implicate GSK-3 in many aspects of cellular metabolism, proliferation, differentiation and development.
In a GSK-3 mediated pathway that is relevant for the treatment of type II diabetes, insulin-induced signaling leads to cellular glucose uptake and glycogen synthesis. Along this pathway, GSK-3 is a negative regulator of the insulin-induced signal. Normally, the presence of insulin causes inhibition of GSK-3 mediated phosphorylation and deactivation of glycogen synthase. The inhibition of GSK-3 leads to increased glycogen synthesis and glucose uptake [Klein et al., PNAS, 93, 8455-9 (1996); Cross et al . , Biochem. J. , 303, 21-26 (1994); Cohen, Biochem. Soc. Trans . , 21, 555-567 (1993); Massillon et al . , Biochem J. 299, 123-128 (1994)]. However, in a diabetic patient where the insulin response is impaired, glycogen synthesis and glucose uptake fail to increase despite the presence of relatively high blood levels of insulin. This leads to abnormally high blood levels of glucose with acute and long term effects that may ultimately result in cardiovascular disease, renal failure and blindness. In such patients, the normal insulin-induced inhibition of GSK-3 fails to occur. It has also been reported that in patients with type II diabetes, GSK-3 is overexpressed [WO 00/38675] . Therapeutic inhibitors of GSK-3 are therefore potentially useful for treating diabetic patients suffering from an impaired response to insulin. GSK-3 activity has also been associated with
Alzheimer's disease. This disease is characterized by the well-known β-amyloid peptide and the formation of intracellular neurofibrillary tangles. The neurofibrillary tangles contain hyperphosphorylated Tau protein where Tau is phosphorylated on abnormal sites. GSK-3 has been shown to phosphorylate these abnormal sites in cell and animal models. Furthermore, inhibition of GSK-3 has been shown to prevent hyperphosphorylation of Tau in cells [Lovestone et al . , Current Biology 4 , 1077-86 (1994); Brownlees et al . , Neuroreport 8, 3251-55 (1997)]. Therefore, it is believed that GSK-3 activity may promote generation of the neurofibrillary tangles and the progression of Alzheimer's disease. Another substrate of GSK-3 is β-catenin which is degradated after phosphorylation by GSK-3. Reduced levels of β-catenin have been reported in schizophrenic patients and have also been associated with other diseases related to increase in neuronal cell death
[Zhong et al., Nature, 395, 698-702 (1998); Takashima et al., PNAS, 90, 7789-93 (1993); Pei et al . , J. Neuropathol . Exp, 56, 70-78 (1997)].
As a result of the biological importance of GSK-3, there is current interest in therapeutically effective GSK-3 inhbitors . Small molecules that inhibit GSK-3 have recently been reported [WO 99/65897 (Chiron) and WO 00/38675 (SmithKline Beecham) ] . ,
For many of the aforementioned diseases associated with abnormal GSK-3 activity, other protein kinases have also been targeted for treating the same diseases. However, the various protein kinases often act through different biological pathways. For example, certain quinazoline derivatives have been reported recently as inhibitors of p38 kinase (WO 00/12497 to Scios) . The compounds are reported to be useful for treating conditions characterized by enhanced p38- activity and/or enhanced TGF-β activity. While p38 activity has been implicated in a wide variety of diseases, including diabetes, p38 kinase is not reported to be a constituent of an insulin signaling pathway that regulates glycogen synthesis or glucose uptake. Therefore, unlike GSK-3, p38 inhibition would not be expected to enhance glycogen synthesis and/or glucose uptake .
There is a continued need to find new therapeutic agents to treat human diseases. The protein kinases aurora-2 and GSK-3 are especially attractive targets for the discovery of new therapeutics due to their important role in cancer, diabetes, Alzheimer's disease and other diseases .
DESCRIPTION OF THE INVENTION
It has now been found that compounds of this invention and pharmaceutical compositions thereof are effective as protein kinase inhibitors, particularly as inhibitors of aurora-2 and GSK-3. These compounds have the general formula I:
or a pharmaceutically acceptable derivative or prodrug thereof, wherein: Z1 to Z4 are as described below; Ring A is selected from the group consisting of :
a b c d
and
G is Ring C or Ring D;
Ring C is selected from a phenyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, or 1, 2, 4-triazinyl ring, wherein said Ring C has one or two ortho substituents independently selected from -R1, any substitutable non- ortho carbon position on Ring C is independently substituted by -R5, and two adjacent substituents on Ring C are optionally taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-6 membered ring having 0-3 heteroatoms selected from oxygen, sulfur or nitrogen, said fused ring being optionally substituted by halo, oxo, or -R8; Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein Ring D is substituted at any substitutable ring carbon by oxo or -R5, and at any substitutable ring nitrogen by -R4, provided that when Ring D is a six-membered aryl or heteroaryl ring, -R5 is hydrogen at each ortho carbon position of Ring D; R1 is selected from -halo, -CN, -N02, T-V-R6, phenyl, 5-6 membered heteroaryl ring, 5-6 membered heterocyclyl ring, or Cx_6 aliphatic group, said phenyl, heteroaryl, and heterocyclyl rings each optionally substituted by up to three groups independently selected from halo, oxo, or -R8, said Cι_6 aliphatic group optionally substituted with halo, cyano, nitro, or oxygen, or R1 and an adjacent substituent taken together with their intervening atoms form said ring fused to Ring C;
Rx and Rγ are independently selected from T-R3 , or Rx and Rγ are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-8 membered ring having 0-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen, wherein any substitutable carbon on said fused ring formed by Rx and Rγ is substituted by oxo or T-R3, and any substitutable nitrogen on said ring formed by Rx and Rγ is substituted by R4;
T is a valence bond or a C^ alkylidene chain;
R2 and R2' are independently selected from -R, -T-W-R6, or R2 and R2' are taken together with their intervening atoms to form a fused, 5-8 membered, unsaturated or partially unsaturated, ring having 0-3 ring heteroatoms selected from nitrogen, oxygen, or sulfur, wherein each substitutable carbon on said fused ring formed by R2 and R2' is substituted by halo, oxo, -CN, -N02, -R7, or -V-R6, and any substitutable nitrogen on said ring formed by R2 and R2' is substituted by R4;
R3 is selected from -R, -halo, -OR, -C(=0)R, -C02R, -COCOR, -C0CH2C0R, -N02, -CN, -S(0)R, -S(0)2R, -SR, -N(R)2, -C0N(R7)2, -S02N(R7)2, -OC(=0)R, -N(R7)COR, -N(R7) C02 (optionally substituted Cι_6 aliphatic) , -N(R4)N(R)2, -C=NN(R4)2, -C=N-OR, -N (R7) CON(R7) _ , -N(R7)S02N(R7)2, -N(R4)S02R, or -OC (=0) N (R7) 2 ; each R is independently selected from hydrogen or an optionally substituted group selected from Cι-6 aliphatic, C6-ιo aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms ; each R4 is independently selected from -R7, -COR7, -C02(C!_6 aliphatic), -CON(R7)2, or -S02R7, or two R4 on the same nitrogen are taken together to form a 5-8 membered heterocyclyl or heteroaryl ring; each R5 is independently selected from -R, halo, -OR,
-C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -CON(R4)2, -S02N(R4)2, -OC(=0)R, -N(R4)COR, -N(R4) C02(optionally substituted Cι_s aliphatic) , -N(R4)N(R4)2, -C=NN(R4)2, -C=N-OR, -N (R4) CON (R4) 2, -N(R4)S02N(R4)2, -N(R)S02R, or -OC (=0)N(R4) 2, or R5 and an adjacent substituent taken together with their intervening atoms form said ring fused to Ring C; V is -0-, -S-, -SO-, -S02-, -N(R6)S02-, -S02N(R6)-, -N(R6)-, -CO-, -C02-, -N(R6)C0-, -N (R6) C (O) O- , -N(R6)CON(R6) -, -N(R6)S02N(R6) -, -N (R6)N (R6) - ,
-C(0)N(Rs)-, -OC(0)N(R6) -, -C(R6)20-, -C(R6)2S-, -C(R6)2SO-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C (R6) 2N (R6) - , -C(R6)2N(R6)C(0) -, -C(Re)2N(R6)C(0)0-, -C (R6) =NN (R6) - , -C(R6)=N-0-, -C(R6)2N(R6)N(R6) -, -C (R6) 2N (R6) S02N(R6) - , or -C(Rs)2N(Rs)CON(Rs) -;
W is -C(R6)20-, -C(R6)2S-, -C(R6)2SO-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C(R6)2N(R6)-, -CO-, -C02-, -C(RS)OC(0) -, -C(R6)OC(0)N(R6) -, -C (R6) 2N (R6) CO- , -C(R6)2N(R6)C(0)0-, -C(RS)=NN(R6)-, -C(R6)=N-0~, -C(R6)2N(R6)N(R6)-, -C (R6) 2N(Rε) S02N (Rs) - , -C(R6)2N(R6)CON(R6) -, or -CON(R6)-; each R6 is independently selected from hydrogen or an optionally substituted CL-4 aliphatic group, or two R6 groups on the same nitrogen atom are taken together with the nitrogen atom to form a 5-6 membered heterocyclyl or heteroaryl ring; each R7 is independently selected from hydrogen or an optionally substituted C_.6 aliphatic group, or two R7 on the same nitrogen are taken together with the nitrogen to form a 5-8 membered heterocyclyl or heteroaryl ring; each R8 is independently selected from an optionally substituted d-4 aliphatic group, -OR6, -SRe, -COR6, -S02R6, -N(R6)2, -N(R6)N(R6)2, -CN, -N02, -CON(R6)2, or -C02R6; and R9 is selected from -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -CON(R4)2, -S02N(R4)2, -0C(=0)R, -N(R4)COR, -N (R4) C02 (optionally substituted Cα-6 aliphatic) , -N(R)N(R4) 2, -C=NN(R4)2,
-C=N-OR, -N(R4)CON(R4)2, -N (R4) S02N (R4) 2, -N(R4)S02R, or -0C(=0)N(R4)2..
As used herein, the following definitions shall apply unless otherwise indicated. The' hrase "optionally substituted" is used interchangeably with the phrase "substituted or unsubstituted" or with the term N (un) substituted. " Unless otherwise indicated, an optionally substituted group may have a substituent at each substitutable position of the group, and each substitution is independent of the other.
The term "aliphatic" as used herein means straight-chain, branched or cyclic Cχ-Cι hydrocarbons which are completely saturated or which contain one or more units of unsaturation but which are not aromatic . For example, suitable aliphatic groups include substituted or unsubstituted linear, branched or cyclic alkyl, alkenyl, alkynyl groups and hybrids thereof such as (cycloalkyl) alkyl, (eyeloalkenyl) alkyl or (cycloalkyl) alkenyl. The terms "alkyl", "alkoxy" , "hydroxyalkyl", "alkoxyalkyl" , and "alkoxycarbonyl" , used alone or as part of a larger moiety includes both straight and branched chains containing one to twelve carbon atoms. The terms "alkenyl" and "alkynyl" used alone or as part of a larger moiety shall include both straight and branched chains containing two to twelve carbon atoms. The term "cycloalkyl" used alone or as part of a larger moiety shall include cyclic C3-CX2 hydrocarbons which are completely saturated or which contain one or more units of unsaturation, but which are not aromatic .
The terms "haloalkyl" , "haloalkeiiyl" and "haloalkoxy" means alkyl, alkenyl or alkoxy, as the case may be, substituted with one or more halogen atoms. The term "halogen" means F, Cl, Br, or I .
The term "heteroatom" means nitrogen, oxygen, or sulfur and includes any oxidized form of nitrogen and sulfur, and the quaternized form of any basic nitrogen. Also the term "nitrogen" includes a substitutable nitrogen of a heterocyclic ring. As an example, in a saturated or partially unsaturated ring having 0-3 heteroatoms selected from oxygen, sulfur or nitrogen, the nitrogen may be N (as in 3, 4-dihydro-2Jf-pyrrolyl) , NH (as in pyrrolidinyl) or NR+ (as in N-substituted pyrrolidinyl) .
The terms "carbocycle" , "carbocyclyl" , "carbocyclo" , or "carbocyclic" as used herein means an aliphatic ring system having three to fourteen members. The terms "carbocycle", "carbocyclyl", "carbocyclo", or "carbocyclic" whether saturated or partially unsaturated, also refers to rings that are optionally substituted. The terms "carbocycle" , "carbocyclyl" , "carbocyclo" , or "carbocyclic" also include aliphatic rings that are fused to one or more aromatic or nonaromatic rings, such as in a decahydronapht yl or tetrahydronaphthyl, where the radical or point of attachment is on the aliphatic ring. The term "aryl" used alone or as part of a larger moiety as in "aralkyl", "aralkoxy", or "aryloxyalkyl" , refers to aromatic' ring groups having five to fourteen members, such as phenyl, benzyl, phenethyl, 1-naphthyl, 2-naphthyl, 1-anthracyl and 2- anthracyl . The term "aryl" also refers to rings that are optionally substituted. The term "aryl" may be used interchangeably with the term "aryl ring" . "Aryl" also includes fused polycyclic aromatic ring systems in which an aromatic ring is fused to one or more rings . Examples include 1-naphthyl, 2-naphthyl, 1-anthracyl and 2- anthracyl. Also included within the scope of the term "aryl" , as it is used herein, is a group in which an aromatic ring is fused to one or more non-aromatic rings, such as in an indanyl , phenanthridinyl , or tetrahydronaphthyl, where the radical or point of attachment is on the aromatic ring.
The term "heterocycle" , "heterocyclyl" , or "heterocyclic" as used herein includes non-aromatic ring systems having five to fourteen members, preferably five to ten, in which one or more ring carbons, preferably one to four, are each replaced by a heteroatom such as N, O, or S. Examples of heterocyclic rings include 3-1H- benzimidazol-2-one, (1-substituted) -2-oxo-benzimidazol-3- yl, 2-tetrahydrofuranyl, 3-tetrahydrofuranyl, 2- tetrahydropyranyl, 3-tetrahydropyranyl, 4- tetrahydropyranyl, [1, 3] -dioxalanyl, [1, 3] -dithiolanyl, [1,3] -dioxanyl, 2-1etrahydrothiophenyl, 3- tetrahydrothiophenyl, 2-morpholinyl, 3-morpholinyl, 4- morpholinyl, 2-thiomorpholinyl, 3-thiomorpholinyl, 4- thiomorpholinyl, 1-pyrrolidinyl, 2 -pyrrolidinyl, 3- pyrrolidinyl, 1-piperazinyl, 2-piperazinyl, 1- piperidinyl, 2-piperidinyl, 3-piperidinyl, 4-piperidinyl, 4-thiazolidinyl, diazolonyl, N-substituted diazolonyl, 1- phthalimidinyl, benzoxanyl, benzopyrrolidinyl, benzopiperidinyl , benzoxolanyl, benzothiolanyl, and benzothianyl . Also included within the scope of the term "heterocyclyl" 'or "heterocyclic", as it is used herein, is a group in which a non-aromatic heteroatom-containing ring is fused to one or more aromatic or non-aromatic rings, such as in an indolinyl, chromanyl, phenanthridinyl , or tetrahydroquinolinyl, where the radical or point of attachment is on the non-aromatic heteroatom-containing ring. The term "heterocycle" ,
"heterocyclyl" , or "heterocyclic" whether saturated or partially unsaturated, also refers to rings that are optionally substituted.
The term "heteroaryl" , used alone or as part of a larger moiety as in "heteroaralkyl" or
"heteroarylalkoxy" , refers to heteroaromatic ring groups having five to fourteen members. Examples of heteroaryl rings include 2-furanyl, 3-furanyl, N-imidazolyl, 2- imidazolyl, 4-imidazolyl, 5-imidazolyl, 3-isoxazolyl, 4- isoxazolyl, 5-isoxazolyl, 2-oxadiazolyl, 5-oxadiazolyl, 2-oxazolyl, 4-oxazolyl, 5-oxazolyl, 1-pyrrolyl, 2- pyrrolyl, 3-pyrrolyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, 2- pyrimidyl, 4-pyrimidyl, 5-pyrimidyl, 3-pyridazinyl, 2- thiazolyl, 4-thiazolyl, 5-thiazolyl, 5-tetrazolyl, 2- triazolyl, 5-triazolyl, 2-thienyl, 3-thienyl, carbazolyl, benzimidazolyl, benzothienyl , benzofuranyl, indolyl, quinolinyl, benzotriazolyl, benzothiazolyl, benzooxazolyl, benzimidazolyl, isoquinolinyl, indolyl, isoindolyl, acridinyl, or benzoisoxazolyl. Also included within the scope of the term "heteroaryl" , as it is used herein, is a group in which a heteroatomic ring is fused to one or more aromatic or nonaromatic rings where the radical or point of attachment is on the heteroaromatic ring. Examples include tetrahydroquinolinyl, tetrahydroisoquinolinyl , and pyrido [3 , 4-d] pyrimidinyl . The term "heteroaryl" also refers to rings that are optionally substituted. The term "heteroaryl" may be used interchangeably with the term "heteroaryl ring" or the term "heteroaromatic" .
An aryl (including aralkyl,, aralkoxy, aryloxyalkyl and the like) or heteroaryl (including heteroaralkyl and heteroarylalkoxy and the like) group may contain one or more substituents . Examples of suitable substituents on the unsaturated carbon atom of an aryl, heteroaryl, aralkyl, or heteroaralkyl group include a halogen, -R°, -OR°, -SR°, 1, 2-methylene-dioxy, 1, 2-ethylenedioxy, protected OH (such as acyloxy), phenyl (Ph) , substituted Ph, -O(Ph), substituted -O(Ph),
-CH2(Ph), substituted -CH2(Ph), -CH2CH2(Ph), substituted -CH2CH2(Ph), -N02, -CN, -N(R°)2, -NR°C(0)R°, -NR°C (0) N (R°) 2, -NR°C02R°, -NR°NR°C(0)Ro, -NR°NR°C (O) N (R°) 2, -NR°NR°C02R° , -C(0)C(0)R°, -C(0)CH2C(0)R°, -C02R°, -C(0)R°, -C(0)N(R°)2, -0C(0)N(R°)2, -S(0)2R°, -S02N(R°)2, -S(0)R°, -NR°S02N (R°) _ , -NR°S02R°, -C(=S)N(R°)2, -C (=NH) -N (R°) 2, - (CH2) yNHC (0) R°, - (CH2)yNHC(0)CH(V-R°) (R°) ; wherein R° is hydrogen, a substituted or unsubstituted aliphatic group, an unsubstituted heteroaryl or heterocyclic ring, phenyl (Ph) , substituted Ph, -O(Ph), substituted -0 (Ph) ,
-CH2(Ph), or substituted -CH2(Ph); y is 0-6; and V is a linker group. Examples of substituents on the aliphatic group or the phenyl ring of R° include amino, alkylamino, dialkylamino, aminocarbonyl, halogen, alkyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminocarbonyloxy, dialkylaminocarbonyloxy, alkoxy, nitro, cyano, carboxy, alkoxycarbonyl , alkylcarbonyl , hydroxy, haloalkoxy, or haloalkyl .
An aliphatic group or a non-aromatic heterocyclic ring may contain one or more substituents . Examples of suitable substituents on the saturated carbon of an aliphatic group or of a non-aromatic heterocyclic ring include those listed above for the unsaturated carbon of an aryl or heteroaryl group and the following: =0, =S, =NNHR*, =NN(R*)2, =N-, =NNHC(0)R*, =NNHC02 (alkyl) , =NNHS02 (alkyl) , or =NR*, where each R* is independently selected from hydrogen, an unsubstituted aliphatic group or a substituted aliphatic group. Examples of substituents on the aliphatic group include amino, alkylamino, dialkylamino, aminocarbonyl, halogen, alkyl, alkylaminocarbonyl , dialkylaminocarbonyl , alkylaminocarbonyloxy, dialkylaminocarbonyloxy, alkoxy, nitro, cyano, carboxy, alkoxycarbonyl, alkylcarbonyl, hydroxy, haloalkoxy, or haloalkyl.
Suitable substituents on the nitrogen of a non- aromatic heterocyclic ring include -R+, -N(R+)2, -C(0)R+, -C02R+, -C(0)C(0)R+, -C (0) CH2C (O) R+, -S02R+, -S02N(R+)2,
-C(=S)N(R+)2, -C(=NH) -N(R+)2, and -NR+S02R+; wherein R+ is hydrogen, an aliphatic group, a substituted aliphatic group, phenyl (Ph) , substituted Ph, -O(Ph), substituted -O(Ph) , CH2(Ph), substituted CH2 (Ph) , or an unsubstituted heteroaryl or heterocyclic ring.
Examples of substituents on the aliphatic group or the phenyl ring include amino, alkylamino, dialkylamino, aminocarbonyl, halogen, alkyl, alkylaminocarbonyl, dialkylaminocarbonyl , alkylaminocarbonyloxy, dialkylaminocarbonyloxy, alkoxy, nitro, cyano, carboxy, alkoxycarbonyl, alkylcarbonyl, hydroxy, haloalkoxy, or haloalkyl . The term "linker group" or "linker" means an organic moiety that connects two parts of a compound. Linkers are typically comprised of an atom such as oxygen or sulfur, a unit such as -NH-, -CH2-, -C(0)-, -C(0)NH-, or a chain of atoms, such as an alkylidene chain. The molecular mass of a linker is typically in the range of about 14 to 200, preferably in the range of 14 to 96 with a length of up to about six atoms. Examples of. linkers include a saturated or unsaturated Cι-6 alkylidene chain which is optionally substituted, and wherein one or two saturated carbons of the chain are optionally replaced by -C(O)-, -C(0)C(0)-, -C0NH-, -CONHNH-, -C02-, -OC(O)-, -NHC02-, -0-, -NHCONH-, -OC(0)NH-, -NHNH- , -NHC0-, -S-, -SO-, -S02-, -NH-, -S02NH-, or -NHS02- .
The term "alkylidene chain" refers to an optionally substituted, straight or branched carbon chain that may be fully saturated or have one or more units of unsaturation. The optional substituents are as described above for an aliphatic group.
A combination of substituents or variables is permissible only if such a combination results in a stable or chemically feasible compound. A stable compound or chemically feasible compound is one in which the chemical structure is not substantially altered when kept at a temperature of 40 °C or less, in the absence of moisture or other chemically reactive conditions, for at least a week.
Unless otherwise stated, structures depicted herein are also meant to include all stereochemical forms of the structure; i.e., the R and S configurations for each asymmetric center. Therefore, single stereochemical isomers as well as enantiomeric and diastereomeric mixtures of the present compounds are within the scope of the invention. Unless otherwise stated, structures depicted herein are also meant to include compounds which differ only in the presence of one or more isotopically enriched atoms. For example, compounds having the present structures except for the replacement of a hydrogen by a deuterium or tritium, or the replacement of a carbon by a 13C- or 14C-enriched carbon are within the scope -of this invention.
Compounds of formula I or salts thereof may be formulated into compositions. In a preferred embodiment, the composition is a pharmaceutical composition. In one embodiment, the composition comprises an amount of the protein kinase inhibitor effective to inhibit a protein kinase, particularly GSK-3, in a biological sample or in a patient. In another embodiment, compounds of this invention and pharmaceutical compositions thereof, which comprise an amount of the protein kinase- inhibitor effective to treat or prevent a GSK-3-mediated condition and a pharmaceutically acceptable carrier, adjuvant, or vehicle, may be formulated for administration to a patient.
The term "GSK-3-mediated condition" or "disease", as used herein, means any disease or other deleterious condition or state in which GSK-3 is known to play a role. Such diseases or conditions include, without limitation, diabetes, Alzheimer's disease, Huntington's Disease, Parkinson's Disease, AIDS- associated dementia, amyotrophic lateral sclerosis (AML) , multiple sclerosis (MS) , schizophrenia, cardiomycete hypertrophy, reperfusion/ischemia, and baldness.
One aspect of this invention relates to a method of enhancing glycogen synthesis and/or lowering blood levels of glucose in a patient in need thereof, which method comprises administering to the patient a therapeutically effective amount of a compound of formula I or a pharmaceutical composition thereof. This method is especially useful for diabetic patients . Another method relates to inhibiting the production of hyperphosphorylated Tau protein, which is useful in halting or slowing the progression of Alzheimer's disease. Another method relates to inhibiting the phosphorylation of β-catenin, which is useful for treating schizophrenia.
Another aspect of the invention relates to inhibiting GSK-3 activity in a biological sample, which method comprises contacting the biological sample with a GSK-3 inhibitor of formula I. Another aspect of this invention relates to a method of inhibiting Aurora-2 activity in a patient, which method comprises administering to the patient a compound of formula I or a composition comprising said compound. Another aspect of this invention relates to a method of treating or preventing an Aurora-2-mediated disease with an Aurora-2 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula I or a pharmaceutical composition thereof .
The term "Aurora-2-mediated condition" or "disease", as used herein, means any disease or other deleterious condition in which Aurora is known to play a role. The term "Aurora-2-mediated condition" or "disease" also means those diseases or conditions that are alleviated by treatment with an Aurora-2 inhibitor. Such conditions include, without limitation, cancer. The term "cancer" includes, but is not limited to the following cancers: colon and ovarian.
Another aspect of the invention relates to inhibiting Aurora-2 activity in a biological sample, which method comprises contacting the biological sample with the Aurora-2 inhibitor of formula I, or a composition thereof.
Another aspect of this invention relates to a method of treating or preventing a CDK-2-mediated diseases with a CDK-2 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula I or a pharmaceutical composition thereof .
The term "CDK-2-mediated condition" or "disease", as used herein, means any disease or other deleterious condition in which CDK-2 is known to play a role. The term "CDK-2-mediated condition" or "disease" also means those diseases or conditions that are alleviated by treatment with a CDK-2 inhibitor. Such conditions include, without limitation, cancer, Alzheimer's disease, restenosis, angiogenesis, glomerulonephritis, cytomegalovirus, HIV, herpes, psoriasis, atherosclerosis, alopecia, and autoimmune diseases such as rheumatoid arthritis. See Fischer, P.M. and Lane, D.P., Current Medicinal Chemistry, 7, 1213-1245 (2000); Mani, S-, Wang, C. , Wu, K. , Francis, R. and Pestell, R., Exp. Opin. Invest . Drugs, 9, 1849 (2000); Fry, D.W. and Garrett, M.D., Current Opinion in Oncologic , Endocrine & Metabolic Invest igational Drugs, 2 , 40-59 (2000) .
Another aspect of the invention relates to inhibiting CDK-2 activity in a biological sample or a patient, which method comprises administering to the patient a compound of formula I or a composition comprising said compound.
Another aspect of this invention relates to a method of treating or preventing an ERK-2-mediated diseases with an ERK-2 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula I or a pharmaceutical composition thereof.
The term "ERK-mediated condition" , as used herein means any disease state or other deleterious condition in which ERK is known to play a role . The term "ERK-2-mediated condition" or "disease" also means those diseases or conditions that are alleviated by treatment with a ERK-2 inhibitor. Such conditions include, without limitation, cancer, stroke, diabetes, hepatomegaly, cardiovascular disease including cardiomegaly, Alzheimer's disease, cystic fibrosis, viral disease, autoimmune diseases, atherosclerosis, restenosis, psoriasis, allergic disorders including asthma, inflammation, neurological disorders and hormone-related diseases. The term "cancer" includes, but is not limited to the following cancers: breast, ovary, cervix, prostate, testis, genitourinary tract, esophagus, larynx, glioblastoma, neuroblastoma, stomach, skin, keratoacanthoma, lung, epidermoid carcinoma, large cell carcinoma, small cell carcinoma, lung adenocarcinoma, bone, colon, adenoma, pancreas, adenocarcinoma, thyroid, follicular carcinoma, undifferentiated carcinoma, papillary carcinoma, seminoma, melanoma, sarcoma, bladder carcinoma, liver carcinoma and biliary passages, kidney carcinoma, myeloid disorders, lymphoid disorders, Hodgkin's, hairy cells, buccal cavity and pharynx (oral), lip, tongue, mouth, pharynx, small intestine, colon- rectum, large intestine, rectum, brain and central nervous system, and leukemia. ERK-2 protein kinase and its implication in various diseases has been described [Bokemeyer et al . 1996, Kidney Int . 49, 1187; Anderson et al., 1990, Nature 343, 651; Crews et al . , 1992, Science 258, 478; Bjorbaek et al . , 1995, J. Biol . Chem. 270, 18848; Rouse et al., 1994, Cell 78, 1027; Raingeaud et al., 1996, Mol . Cell Biol . 16 , 1247; Raingeaud et al . 1996; Chen et al . , 1993 Proc. Natl . Acad. Sci . USA 90, 10952; Oliver et al., 1995, Proc . Soc . Exp. Biol . Med. 210, 162; Moodie et al . , 1993, Science 260, 1658; Frey and Mulder, 1997, Cancer Res . 57, 628; Sivaraman et al . , 1997, J Clin. Invest . 99, 1478; Whelchel et al., 1997, Am. J. Respir. Cell Mol . Biol . 16, 589] . Another aspect of the invention relates to inhibiting ERK-2 activity in a biological sample or a patient, which method comprises administering to the patient a compound of formula I or a composition comprising said compound. Another aspect of this invention relates to a method of treating or preventing an AKT-mediated diseases with an AKT inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula I or a pharmaceutical composition thereof.
The term "AKT-mediated condition" , as used herein, means any disease state or other deleterious condition in which AKT is known to play a role. The term "AKT-mediated condition" or "disease" also means those diseases or conditions that are alleviated by treatment with a AKT inhibitor . AKT-mediated diseases or conditions include, but are not limited to, proliferative disorders, cancer, and neurodegenerative disorders. The association of AKT, also known as protein kinase B, with various diseases has been described [Khwaja, A. , Nature, pp. 33-34, 1990; Zang, Q. Y. , et al, Oncogene, 19 2000; Kazuhiko, N. , et al, The Journal of Neuroscience, 20 2000] .
Another aspect of the invention relates to inhibiting AKT activity in a biological sample or a patient, which method comprises administering to the patient a compound of formula I or a composition comprising said compound.
Another aspect of this invention relates to a method of treating or preventing a Src-mediated disease with a Src inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula I or a pharmaceutical composition thereof .
The term "Src-mediated condition", as used herein means any disease state or other deleterious condition in which Src is known to play a role. The term "Src-mediated condition" or "disease" also means those diseases or conditions that are alleviated by treatment with a Src inhibitor. Such conditions include, without limitation, hypercalcemia, osteoporosis, osteoarthritis, cancer, symptomatic treatment of bone metastasis, and Paget's disease. Src protein kinase and its implication in various diseases has been described [Soriano, Cell , 69 , 551 (1992); Soriano et al . , Cell , 64, 693 (1991); Takayanagi, J". Clin. Invest . , 104, 137 (1999); Boschelli, Drugs of the Future 2000, 25(7), 717, (2000); Talamonti, J". Clin. Invest . , 91, 53 (1993); Lutz, Biochem. Biophys. Res. 243, 503 (1998); Rosen, J. Biol . Chem. , 261, 13754 (1986); Bolen, Proc. Natl . Acad. Sci . USA, 84, 2251 (1987); Masaki, Hepatology, 27, 1257 (1998); Biscardi,
Adv. Cancer Res. , 16 , 61 (1999); Lynch, Leukemia, 7, 1416 (1993); Wiener, Clin. Cancer Res . , 5, 2164 (1999); Staley, Cell Growth Diff. , 8, 269 (1997)].
Another aspect of the invention relates to inhibiting Src activity in a biological sample or a patient, which method comprises administering to the patient a compound of formula I or a composition comprising said compound.
The term "pharmaceutically acceptable carrier, adjuvant, or vehicle" refers to a non-toxic carrier, adjuvant, or vehicle that may be administered to a patient, together with a compound of this invention, and which does not destroy the pharmacological activity thereof . The term "patient" includes human and veterinary subjects.
The term "biological sample", as used herein, includes, without limitation, cell cultures or extracts thereof; preparations of an enzyme suitable for in vitro assay,- biopsied material obtained from a mammal or extracts thereof; and blood, saliva, urine, feces, semen, tears, or other body fluids or extracts thereof.
The amount effective to inhibit protein kinase for example, GSK-3 and Aurora-2, is one that measurably inhibits the kinase activity where compared to the activity of the enzyme in the absence of an inhibitor.' Any method may be used to determine inhibition, such as, for example, the Biological Testing Examples described below.
Pharmaceutically acceptable carriers that may be used in these pharmaceutical compositions include, but are not limited to, ion exchangers, alumina, aluminum stearate, lecithin, serum proteins, such as human serum albumin, buffer substances such as phosphates, glycine, sorbic acid,' potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes, such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride, zinc salts, colloidal silica, magnesium trisilicate, polyvinyl pyrrolidone, cellulose-based substances, polyethylene glycol, sodium carboxymethylcellulose, polyacrylates, waxes, polyethylene-polyoxypropylene-block polymers , polyethylene glycol and wool fat .
The compositions of the present invention may be administered orally, parenterally, by inhalation spray, topically, rectally, nasally, buccally, vaginally or via an implanted reservoir. The term "parenteral" as used herein includes subcutaneous, intravenous, intramuscular, intra-articular, intra-synovial, intrasternal, intrathecal, intrahepatic , intralesional and intracranial injection or infusion techniques.
Preferably, the compositions are administered orally, intraperitoneally or intravenously.
Sterile injectable forms of the compositions of this invention may be aqueous or oleaginous suspension. These suspensions may be formulated according to techniques known in the art using suitable dispersing or wetting agents and suspending agents . The sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally- acceptable diluent or solvent, for example as a solution in 1, 3-butanediol . Among the acceptable vehicles and solvents that may be employed are water, Ringer's solution and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose, any bland fixed oil may be employed including synthetic mono- or di-glycerides. Fatty acids, such as oleic acid and its glyceride derivatives are useful in the preparation of injectables, as are natural pharmaceutically- acceptable oils, such as olive oil or castor oil, especially in their polyoxyethylated versions. These oil solutions or' suspensions may also contain a long-chain alcohol diluent or dispersant, such as carboxymethyl cellulose or similar dispersing agents which are commonly used in the formulation of pharmaceutically acceptable dosage forms including emulsions and suspensions . Other commonly used surfactants, such as Tweens, Spans and other emulsifying agents or bioavailability enhancers which are commonly used in the manufacture of pharmaceutically acceptable solid, liquid, or other dosage forms may also be used for the purposes of formulation. The pharmaceutical compositions of this invention may be orally administered in any orally acceptable dosage form including, but not limited to, capsules, tablets, aqueous suspensions or solutions. In the case of tablets for oral use, carriers commonly used include lactose and corn starch. Lubricating agents, such as magnesium stearate, are also typically added. For oral administration in a capsule form, useful diluents include lactose and dried cornstarch. When aqueous suspensions are required for oral use, the active ingredient is combined with emulsifying and suspending agents. If desired, certain sweetening, flavoring or coloring agents may also be added. Alternatively, the pharmaceutical compositions of this invention may be administered in the form of suppositories for rectal administration. These can' be prepared by mixing the agent with a suitable non- irritating excipient which is solid at room temperature but liquid at rectal temperature and therefore will melt in the rectum to release the drug. Such materials include cocoa butter, beeswax and polyethylene glycols.
The pharmaceutical compositions of this invention may also be administered topically, especially when the target of treatment includes areas or organs readily accessible by topical application, including diseases of the eye, the skin, or the lower intestinal tract . Suitable topical formulations are readily prepared for each of these areas or organs . Topical application for the lower intestinal tract can be effected in a rectal suppository formulation (see above) or in a suitable enema formulation. Topically-transdermal patches may also be used.
For topical applications, the pharmaceutical compositions may be formulated in a suitable ointment containing the active component suspended or dissolved in one or more carriers. Carriers for topical administration of the compounds of this invention include, but are not limited to, mineral oil, liquid petrolatum, white petrolatum, propylene glycol, polyoxyethylene, polyoxypropylene compound, emulsifying wax and water. Alternatively, the pharmaceutical compositions can be formulated in a suitable lotion or cream containing the active components suspended or dissolved in one or more pharmaceutically acceptable carriers. Suitable carriers include, but are not limited to, mineral oil, sorbitan monostearate, polysorbate 60, cetyl esters wax, cetearyl alcohol, 2-octyldodecanol, benzyl alcohol and water.
For ophthalmic use, the pharmaceutical compositions may be formulated as micronized suspensions in isotonic, pH adjusted sterile saline, or, preferably, as solutions in isotonic, pH adjusted sterile saline, either with or without a preservative such as benzylalkonium chloride. Alternatively, for ophthalmic uses, the pharmaceutical compositions may be formulated in an ointment such as petrolatum. The pharmaceutical compositions of this invention may also be administered by nasal aerosol or inhalation. Such compositions are prepared according to techniques well-known in the art of pharmaceutical formulation and may be prepared as solutions in saline, employing benzyl alcohol or other suitable preservatives, absorption promoters to enhance bioavailability, fluorocarbons, and/or other conventional solubilizing or dispersing agents .
In addition -to the compounds of this invention, pharmaceutically acceptable derivatives or prodrugs of the compounds of this invention may also be employed in compositions to treat or prevent the above-identified diseases or disorders.
A "pharmaceutically acceptable derivative or prodrug" means any pharmaceutically acceptable salt, ester, salt of an ester or other derivative of a compound of this invention which, upon administration to a recipient, is capable of providing, either directly or indirectly, a compound of this invention or an inhibitorily active metabolite or residue thereof . Particularly favored derivatives or prodrugs are those that increase the bioavailability of the compounds of this invention when such compounds are administered to a patient (e.g., by allowing an orally administered compound to be more readily absorbed into the blood) or which enhance delivery of the parent compound to a biological compartment (e.g., the brain or lymphatic system) relative to the parent species.
Pharmaceutically acceptable prodrugs of the compounds of this invention include, without limitation, esters, amino acid esters, phosphate esters, metal salts and sulfonate esters . Pharmaceutically acceptable salts of the compounds of this invention include those derived from pharmaceutically acceptable inorganic and organic acids and bases . Examples of suitable acid salts include acetate, adipate, alginate, aspartate, benzoate, benzenesulfonate, bisulfate, butyrate, citrate, camphorate, camphorsulfonate, cyclopentanepropionate, digluconate, dodecylsulfate, ethanesulfonate, formate, fumarate, glucoheptanoate, glycerophosphate, glycolate, hemisulfate, heptanoate, hexanoate, hydrochloride, hydrobromide, hydroiodide, 2-hydroxyethanesulfonate, lactate, maleate, malonate, methanesulfonate, 2- naphthalenesulfonate, nicotinate, nitrate, oxalate, palmoate, pectinate, persulfate, 3-phenylpropionate, phosphate, picrate, pivalate, propionate, salicylate, succinate, sulfate, tartrate, thiocyanate, tosylate and undecanoate. Other acids, such as oxalic, while not in themselves pharmaceutically acceptable, may be employed in' the preparation of salts useful as intermediates in obtaining the compounds of the invention and their pharmaceutically acceptable acid addition salts .
Salts derived from appropriate bases include alkali metal (e.g., sodium and potassium), alkaline earth metal (e.g., magnesium), ammonium and N+(Cι-4 alkyl) 4 salts. This invention also envisions the quaternization of any basic nitrogen-containing groups of the compounds disclosed herein. Water or oil-soluble or dispersible products may be obtained by such quaternization. The amount of the protein kinase inhibitor that may be combined with the carrier materials to produce a single dosage form will vary depending upon the patient treated and the particular mode of administration. Preferably, the compositions should be formulated so that a dosage of between 0.01 - 100 mg/kg body weight/day of the inhibitor can be administered to a patient receiving these compositions .
It should also be understood that a specific dosage and treatment regimen for any particular patient will depend upon a variety of factors, including the activity of the specific compound employed, the age, body weight, general health, sex, diet, time of administration, rate of excretion, drug combination, and the judgment of the treating physician and the severity of the particular disease being treated. The amount of the inhibitor will also depend upon the particular compound in the composition.
Depending upon the particular protein kinase- mediated condition to be treated or prevented, additional therapeutic agents, which are normally administered to treat or prevent that condition, may be administered together with the inhibitors of this invention. For example, in the treatment of diabetes other anti-diabetic agents may be combined with the GSK-3 inhibitors of this invention to treat diabetes. These agents include, without limitation, insulin or insulin analogues, in injectable or inhalation form, glitazones, alpha glucosidase inhibitors, biguanides, insulin sensitizers, and sulfonyl ureas .
Other examples of agents the inhibitors of this invention may also be combined with include, without limitation, chemotherapeutic agents or other anti- proliferative agents such as adriamycin, dexamethasone, vincristine, cyclophosphamide, fluorouracil, topotecan, taxol, interferons, and platinum derivatives; anti- inflammatory agents such as corticosteroids, TNF blockers, IL-1 RA, azathioprine, cyclophosphamide, and sulfasalazine; immunomodulatory and immunosuppressive agents such as cyclosporin, tacrolimus, rapamycin, mycophenolate mofetil, interferons, corticosteroids, cyclophophamide, .azathioprine, and sulfasalazine; neurotrophic factors such as acetylcholinesterase inhibitors, MAO inhibitors, interferons, anti- convulsants, ion channel blockers, riluzole, and anti- Parkinsonian agents; agents for treating cardiovascular disease such as beta-blockers, ACE inhibitors, diuretics, nitrates, calcium channel blockers, and statins; agents for treating liver disease such as corticosteroids, cholestyramine, interferons, and anti-viral agents; agents for treating blood disorders such as corticosteroids, anti-leukemic agents, and growth factors; and agents for treating immunodeficiency disorders such as gamma globulin.
Those additional agents may be administered separately from the protein kinase inhibitor-containing composition, as part of a multiple dosage regimen. Alternatively, those agents may be part of a single dosage form, mixed together with the protein kinase inhibitor of this invention in a single composition. Compounds of this invention may exist in alternative tautomeric forms, as in tautomers 1 and 2 shown below. Unless otherwise indicated, the representation of either tautomer is meant to include the other.
1 2
R and Ry (at positions Z3 and Z4, respectively) may be taken together to form a fused ring, providing a bicyclic ring system containing Ring A. Preferred Rx/Rγ rings include a 5-, 6-, 7-, or 8-membered unsaturated or partially unsaturated ring having 0-2 heteroatoms, wherein said Rx/Rγ ring is optionally substituted. Examples of Ring A systems are shown below by compounds I-A through I-DD, wherein Z1 is nitrogen or C(R9) and Z2 is nitrogen or C(H) .
I-A I-B I-C
I-D I-E I-F
I-G I-H I-I
I-J I-K I-L
I-M I-N 1-0
I-P I-Q I-R
I-S I -T I -U
I -V I - I -X
i -y I - Z I-AA
I-BB I -CC I -DD
Preferred bicyclic Ring A systems include I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I, I-J, I-K, I-L, and I-M, more preferably I-A, I-B, I-C, I-F, and I-H, and most preferably I-A, I-B, and I-H. In the monocyclic Ring A system, preferred Rx groups, when present, include hydrogen, alkyl- or dialkylamino, acetamido, or a Cι_4 aliphatic group such as methyl, ethyl, cyclopropyl, isopropyl or t-butyl. Preferred Ry groups, when present, include T-R3 wherein T is a valence bond or a methylene, and R3 is -R, -N(R4)2, or -OR. Examples of preferred Ry include 2-pyridyl, 4- pyridyl, piperidinyl, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, alkyl- or dialkylamino, acetamido, optionally substituted phenyl such as phenyl or halo- substituted phenyl, and methoxymethyl .
In the bicyclic Ring A system, the ring formed when Rx and Rγ are taken together may be substituted or unsubstituted. Suitable substituents include -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -C0N(R4)2, -S02N(R4)2, -0C(=0)R, -N(R4)C0R, -N(R4) C02 (optionally substituted ^e aliphatic) , -N(R)N(R4)2, -C=NN(R4)2, -C=N-OR, -N(R4) C0N(R4) _ , -N(R)S02N(R4)2, -N(R4)S02R, or -OC (=0) N(R4) 2, wherein R and R4 are as defined above. Preferred Rx/Rγ ring substituents include -halo, -R, -OR, -COR, -C02R,
-C0N(R4)2, -CN, or -N(R4)2 wherein R is hydrogen or an optionally substituted Cι-6 aliphatic group.
R2 and R2' may be taken together to form a fused ring, thus providing a bicyclic ring system containing a pyrazole ring. Preferred fused rings include benzo, pyrido, pyrimido, and a partially unsaturated 6-membered carbocyclo ring, wherein said fused ring is optionally substituted. These are exemplified in the following formula I compounds having a pyrazole-containing bicyclic ring system:
Preferred substituents on the R2/R2' fused ring include one or more of the following: -halo, -N(R4)2, -Cι_3 alkyl, -Cι_3 haloalkyl, -N02, -0.(Cι-3 alkyl) , -C02(Cι-3 alkyl), -CN, -S02 (Cι.3 alkyl) , -S02NH2, -OC(0)NH2/ - NH2S02(C1.3 alkyl) , -NHC (0) (Cι-3 alkyl) , -C(0)NH2, and -C0(Cι- 3 alkyl) , wherein the (Cχ,3 alkyl) is most preferably methyl .
When the pyrazole ring system is monocyclic, preferred R2 groups include hydrogen, Cx. aliphatic, alkoxycarbonyl, (un) substituted phenyl, hydroxyalkyl, alkoxyalkyl, aminocarbonyl, mono- or dialkylaminocarbonyl, aminoalkyl , alkylaminoalkyl , dialkylaminoalkyl , phenylaminocarbonyl, and (N- heterocyclyl) carbonyl . Examples of such preferred R2 substituents include methyl, cyclopropyl, ethyl, isopropyl, propyl, t-butyl, cyclopentyl, phenyl, C02H, C02CH3, CH20H, CH2OCH3, CH2CH2CH2OH, CH2CH2CH2OCH3, CH2CH2CH2OCH2Ph, CH2CH2CH2NH2 , CH2CH2CH2NHCOOC (CH3) 3 , CONHCH(CH3.)2, CONHCH2CH=CH2, CONHCH2CH2OCH3 , C0NHCH2Ph, CONH(cyclohexyl) , CON(Et)2, CON(CH3) CH2Ph, CONH (n-C3H7) , CON(Et)CH2CH2CH3, C0NHCH2CH (CH3) _ , CON (n-C3H7) 2, CO (3- methoxymethylpyrrolidin-1-yl) , CONH (3-tolyl) , CONH (4- tolyl) , CONHCH3, CO(morpholin-l-yl) , C0(4-methylpiperazin- 1-yl) , CONHCH2CH2OH, C0NH2 , and CO (piperidin-1-yl) . A preferred R2' group is hydrogen.
An embodiment that is particularly useful for treating GSK3 -mediated diseases relates to compounds of formula II :
II or a pharmaceutically acceptable derivative or prodrug thereof, wherein; Ring C is selected from a phenyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, or 1, 2, 4-triazinyl ring, wherein said Ring C has one or two ortho substituents independently selected from -R1, any substitutable non- ortho carbon position on Ring C is independently substituted by -R5, and two adjacent substituents on Ring C are optionally taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-6 membered ring having 0-3 heteroatoms selected from oxygen, sulfur or nitrogen, said fused ring being optionally substituted by halo, oxo, or -R8; R1 is selected from -halo, -CN, -N02, T-V-R6, phenyl, 5-6 membered heteroaryl ring, 5-6 membered heterocyclyl ring, or C .6 aliphatic group, said phenyl, heteroaryl, and heterocyclyl rings each optionally substituted by up to three groups independently selected from halo, oxo, or -R8, said _.5 aliphatic group optionally substituted with halo, cyano, nitro, or oxygen, or R1 and an adjacent substituent taken together with their intervening atoms form said ring fused to Ring C; Rx and Ry are independently selected from T-R3, or Rx and Ry are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-8 membered ring having 0-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen, wherein any substitutable carbon on said fused ring formed by Rx and Rγ is substituted by oxo or T-R3, and any substitutable nitrogen on said ring formed by Rx and Ry is substituted by R4;
T is a valence bond or a Cι_4 alkylidene chain;
R2 and R2' are independently selected from -R, -T-W-R6, or R2 and R2' are taken together with their intervening atoms to form a fused, 5-8 membered, unsaturated or partially unsaturated, ring having 0-3 ring heteroatoms selected from nitrogen, oxygen, or sulfur, wherein each substitutable carbon on said fused ring formed by R2 and R2' is substituted by halo, oxo, -CN, -N02, -R7, or -V-R6, and any substitutable nitrogen on said ring formed by R2 and R2' is substituted by R4;
R3 is selected from -R, -halo, -OR, -C(=0)R, -C02R, -COCOR, -COCH2COR, -N02, -CN, -S(0)R, -S(0)2R, -SR, -N(R)2, -CON(R7)2, -S02N(R7)2,-0C(=0)R, -N(R7)C0R, -N(R7) C0 (optionally substituted Ci-e aliphatic) , -N(R)N(R4)2, -C=NN(R4)2, -C=N-OR, -N (R7) CON (R7) 2, -N(R7)S02N(R7)2, -N(R4)S02R, or -OC (=0)N(R7) 2; each R is independently selected from hydrogen or an optionally substituted group selected from C-6 aliphatic, C6-ι0 aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms ; each R4 is independently selected, from -R7, -COR7,
-C02 (optionally substituted Cx-6 aliphatic) , -CON(R7) , or -S02R7, or two R4 on the same nitrogen are taken together to form a 5-8 membered heterocyclyl or heteroaryl ring; each R5 is independently selected from -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -CON(R4)2, -S02N(R)2, -OC(=0)R, -N(R4)COR, -N(R4) C02 (optionally substituted Cι-6 aliphatic) , -N(R4)N(R4)2, -C=NN(R4)2, -C=N-0R, -N (R4) CON (R4) 2,
-N(R4)S02N(R4)2, -N(R4)S02R, or -OC (=0)N(R4) 2, or R5 and an adjacent substituent taken together with their intervening atoms form said ring fused to Ring C; V is -0-, -S-, -SO-, -S02-, -N(R6)S02-, -S02N(R6)-, -N(R6)-, -CO-, -C02-, -N(R6)CO-, -N(R6) C (O) O- , -N(R6)CON(R6) -, -N(R6)S02N(R6)-, -N (R6) N (R6) - , -C(0)N(R6)-, -OC(0)N(R6)-, -C(R6)20-, -C(R6)2S-, -C(R6)2SO-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C (R6) 2N (R6) - , -C(R6)2N(R6)C(0) -, -C(R6)2N(R6)C(0)0-, -C (R6) =NN(R6) - , -C(R6)=N-0- -C(R6)2N(R6)N(R6)-, -C (R6) 2N (Re) S02N(R6) - , or -C(R6)2N(R6)CON(Rs) -; W is -C(R6)20-, -C(R6)2S-, -C(R6)2SO-, -C(R6)2S02-, -C(Rs)2S02N(R6)-, -C(R6)2N(R6)-, -CO-, -C02-, -C(R6)OC(0) -, -C(R6)OC(0)N(R6) -, -C (R6) 2N (R6) CO- , -C(R6)2N(R6)C(0)0-, -C(R6)=NN(R6) -, -C(Rs)=N-0-, -C(R6)2N(RS)N(R6) -, -C(Rε)2N(R6)S02N(Rs) -, -C(R6)2N(R€)CON(R6)-, or -CON(Rδ)-; each R6 is independently selected from hydrogen, an optionally substituted Cι_4 aliphatic group, or two R6 groups on the same nitrogen atom are taken together with the nitrogen atom to form a 5-6 membered heterocyclyl or heteroaryl ring; each R7 is independently selected from hydrogen or an optionally substituted Cι-6 aliphatic group, or two R7 on the same nitrogen are taken together with the nitrogen- to form a 5-8 membered heterocyclyl or heteroaryl ring; and each R8 is independently selected from an optionally substituted Cι_4 aliphatic group, -OR6, -SR6, -COR6, -S02R6, -N(R6)2, -N(R6)N(R6)2, -CN, -NO,, -CON(R6)2, or -C02R6.
When the Rx and Rγ groups of formula II are taken together to form a fused ring, preferred Rx/Rγ rings include a 5-, 6-, 7-, or 8-membered unsaturated or partially unsaturated ring having 0-2 heteroatoms, wherein said Rx/Rγ ring is optionally substituted. This provides a bicyclic- ring system containing a pyrimidine ring. Examples of preferred pyrimidine ring systems of formula II are the mono- and bicyclic systems shown below.
II-A II-B II-C
II-D II -E II -F
I -G I I-H II-I
I -J II-K II-L
I -M II-N II-O
II-P
More preferred pyrimidine ring systems of formula ΪI include II-A, II-B, II-C, I-F, and II-H, most preferably II-A, I-B, and -II-H.
In the monocyclic pyrimidine ring system of formula II, preferred Rx groups include hydrogen, alkyl- or dialkylamino, acetamido, or a Ci_4 aliphatic group such as methyl, ethyl, cyclopropyl, isopropyl or t-butyl. Preferred RY groups include T-R3 wherein T is a valence bond or a methylene, and R3 is -R, -N(R4)2, or -OR. When R3 is -R or -OR, a preferred R is an optionally substituted group selected from Cι_6 aliphatic, phenyl, or a 5-6 membered heteroaryl or heterocyclyl ring. Examples of preferred Ry include 2-pyridyl, 4-pyridyl, piperidinyl, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, alkyl- or dialkylamino, acetamido, optionally substituted phenyl such as phenyl or halo-substituted phenyl, and ethoxymethyl .
In the bicyclic pyrimidine ring system of formula II, the ring formed when Rx and Rγ are taken together may be substituted or unsubstituted. Suitable substituents include -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R)2, -C0N(R)2, -S02N(R)2, -0C(=0)R, -N(R)C0R, -N (R4) C02 (optionally substituted Cχ-6 aliphatic) , -N(R4)N(R4) , -C=NN(R4)2, -C=N-OR, ' -N(R4)C0N(R4)2, -N(R4) S02N (R4) _ , -N(R)S02R, or -OC(=0)N(R4) 2, wherein R and R4 are as defined above. Preferred Rx/Rγ ring substituents include -halo, -R, -OR, -COR, -C02R, -CON(R4)2, -CN, or -N(R4)2 wherein R is an optionally substituted Cχ_e aliphatic group. The R2 and R2' groups of formula II may be taken together to form a fused ring, thus providing a bicyclic ring system containing a pyrazole ring. Preferred fused rings include benzo, pyrido, pyrimido, and a partially unsaturated 6-membered carbocyclo ring. These are exemplified in the following formula II compounds having a pyrazole-containing bicyclic ring system:
Preferred substituents on the R2/R2' fused ring of formula II include one or more of the following: -halo, -N(R4)2, -Cx-4 alkyl, haloalkyl, -N02, -0(Cι-4 alkyl), -C02 (Cι-4 alkyl) , -CN, -S02 (Cx-4 alkyl) , -S02NH2, -OC(0)NH2, -NH2S02(C1-4 alkyl) , -NHC(O) (Cχ-4 alkyl) , -C(0)NH2, and -CO(C!-4 alkyl), wherein the (Cι_4 alkyl) is a straight, branched, or cyclic alkyl group. Preferably, the (Cι-4 alkyl) group is methyl.
When the pyrazole ring system of formula II is monocyclic, preferred R2 groups include hydrogen, a substituted or unsubstituted group selected from aryl, heteroaryl, or a Cλ.6 aliphatic group. Examples of such preferred R2 groups include methyl, t-butyl, -CH2OCH3, cyclopropyl, furanyl, thienyl, and phenyl. A preferred R2' group is hydrogen.
More preferred ring systems of formula II are the following, which may be substituted as described above, wherein R2 and R2' are taken together with the pyrazole ring to form an indazole ring; and Rx and Ry are each methyl, or Rx and Rγ are taken together with the pyrimidine ring to form a quinazoline or tetrahydroquinazoline ring:
II-Aa II-Ba II-Ha
Particularly preferred are those compounds of formula II-Aa, II-Ba, or II-Ha wherein ring C is a phenyl ring and R1 is halo, methyl, or trifluoromethyl.
Preferred formula II Ring C groups are phenyl and pyridinyl. When two adjacent substituents on Ring C are taken together to form a fused ring, Ring C is contained in a bicyclic ring system. Preferred fused rings include a benzo or pyrido ring. Such rings preferably are fused at ortho and meta positions of Ring C. Examples of preferred bicyclic Ring C systems include naphthyl, quinolinyl and isoquinolinyl .
An important feature of the formula II compounds is the R1 ortho substituent on Ring C. An ortho position on Ring C or Ring D is defined relative to the - position where Ring A is attached. Preferred R1 groups include -halo, an optionally substituted Cx.6 aliphatic group, phenyl, -COR6, -OR6, -CN, -S02R6, -S02NH2, -N(R6)2, -C02R6, -C0NH2, -NHCOR6, -OC(0)NH2, or -NHS02R6. When R1 is an optionally substituted Cι_6 aliphatic group, the most preferred optional substituents are halogen. Examples of preferred R1 groups include -CF3, -Cl, -F, -CN, -C0CH3,
-0CH3, -OH, -CH2CH3, -0CH2CH3, -CH3, -CF2CH3, cyclohexyl, t- butyl, isopropyl, cyclopropyl, -C≡CH, -C≡C-CH3, -S02CH3, -S02NH2, -N(CH3)2, -C02CH3, -C0NH2, -NHC0CH3 , -0C(0)NH2, -NHS02CH3, and -OCF3. On Ring C of formula II, preferred R5 substituents, when present, include -halo, -CN, -N02, -N(R4)2, optionally substituted Cχ-e aliphatic group, -OR, -C(0)R, -C02R, -CONH(R4), -N(R4)COR, -S02N(R4)2, and -N(R4)S02R. More preferred R5 substituents include -Cl, -F, -CN, -CF3, -NH2, -NH(CX-4 aliphatic), -N(Cι-4 aliphatic)2, -0(Cι-4 aliphatic), Cι_ aliphatic, and -C02(Cι_4 aliphatic) . Examples of such preferred Rs substituents include -Cl, -F, -CN, -CF3, -NH2, -NHMe, -NMe2, -OEt, methyl, ethyl, cyclopropyl, isopropyl, . t- butyl, and -C02Et.
Preferred formula II compounds have one or more, and more preferably all, of the features selected from the group consisting of-. (a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is selected from a * naphthyl, quinolinyl or isoquinolinyl ring;
(b) Rx is hydrogen or Cι-4 aliphatic and Rγ is T-R3 , or Rx and Rγ are taken together with their intervening atoms to form an optionally substituted 5-7 membered unsaturated or partially unsaturated ring having 0-2 ring nitrogens;
(c) R1 is -halo, an optionally substituted Cx_e aliphatic group, phenyl, -COR6, -OR6, -CN, -S02R6, -S02NH2, -N(R6)2, -C02R6, -CONH2, -NHCOR6, -OC(0)NH2, or -NHS02R6; and (d) R2' is hydrogen and R2 is hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a Cχ-6 aliphatic group, or R2 and R2' are taken together with their intervening atoms to form a substituted or unsubstituted benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring.
More preferred compounds of formula II have one or more, and more preferably all, of the features selected from the group consisting of:
(a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is a naphthyl ring;
(b) R is hydrogen or methyl and Rγ is -R, N(R4)2, or -OR, or Rx and Rγ are taken together with their intervening atoms to form a 5-7 membered unsaturated or partially unsaturated carbocyclo ring optionally substituted with -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -NO2, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -C0N(R4)2, -S02N(R4)2, -OC(=0)R, -N(R4)COR, -N(R4) C02 (optionally substituted Cι-6 aliphatic) , ~N(R4)N(R4) 2, -C=NN(R4)2, -C=N-OR, -N(R)CON(R4)2, -N (R4) S02N (R4) 2, -N(R4)S02R, or -OC(=0)N(R4)2; (c) R1 is -halo, a Cι_6 haloaliphatic group, a
Cι-6 aliphatic group, phenyl, or -CN;
(d) R2' is hydrogen and R2 is hydrogen or a substituted or unsubstituted group selected from aryl, or a Cι-6 aliphatic group, or R2 and R2' are taken together with their intervening atoms to form a substituted or unsubstituted benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring; and
(e) each R5 is independently selected from -halo, -CN, -N02, -N(R4)2, optionally substituted Cι_6 • aliphatic group , -OR, -C(0)R, -C02R, -CONH(R4), -N(R)C0R,
-S02N(R)2, or -N(R4)S02R.
Even more preferred compounds of formula II have one or more, and more preferably all, of the features selected from the group consisting of: (a) Ring C is a phenyl ring optionally substituted by -R5;
(b) Rx is hydrogen or methyl and Ry is methyl, methoxymethyl, ethyl, cyclopropyl, isopropyl, t-butyl, alkyl- or an optionally substituted group selected from 2-pyridyl, 4-pyridyl, piperidinyl, or phenyl, or Rx and Ry are taken together with their intervening atoms to form an optionally substituted benzo ring or partially unsaturated 6-membered carbocyclo ring;
(c) R1 is -halo, a Cι_4 aliphatic group optionally substituted with halogen, or -CN;
(d) R2 and R2' are taken together with their intervening atoms to form a benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring optionally substituted with -halo, -N(R4)2, -Cι_4 alkyl, -Ci-4 haloalkyl, -N02, -0 (Cι_4 alkyl) , -C02 (Cι_4 alkyl) , -CN, -S02(C1_4 alkyl) , -S02NH2, -OC(0)NH2, -NH2S02 (Cι_4 alkyl) , NHC(O) (C1-4 alkyl) , -C(0)NH2, or -CO (C^ alkyl) , wherein the (Cχ-4 alkyl) is a straight, branched, or cyclic alkyl group; and
(e) each R5 is independently selected from -Cl, -F, -CN, -CF3, -NH2, -NH(Cι_4 aliphatic), -N(C1.4 aliphatic)2, -0(Cι-4 aliphatic), Cι-4 aliphatic, and -C02(Ci-4 aliphatic).
Representative compounds of formula II are shown below in Table 1.
Table 1
II-4 II- 5 II- 6 '
II- 7 II-8 II-9
-10 -11 -12
11-16 11-17 11-18
11-19 11-20 11-21
11-22 11-23 11-24
11-28 11-29 11-30
11-31 11-32 11-33
•11-34 11-35 11-36
11-40 11-41 11-42
11-43 11-44 11-45
11-46 11-47 11-48
11-49 11-50 11-51
11-55 11-56 11-57
11-58 11-59 11-60
-67 -68 11-69
11-73 11-74 11-75
11-76 11-77 11-78
11-82 11-83 11-84
11-85 11-86 11-87
11-88 11-89 11-90
11-91 11-92 11-93
11-94 11-95 11-96
11-97 11-98 11-99
11-103 11-104 11-105
-106 11-107 -108
11-112 11-113 11-114
-124 -125 11-126
11-127 .11-128 11-129
11-130 11-131 11-132
11-142 11-143 11-144
11-145 11-146 11-147
11-148 11-149 11-150
11-151 11-152 11-153
11-157' 11-158 11-159
-160 11-161 11-162
11-166 11-167 11-168
11-169 11-170 11-171
11-172 11-173 11-174
11-175 11-176 11-177
11-178 11-179 11-180
-181 1 -182 -183
11-184 11-185 11-186
11-187 11-188 11-189
-190 11-191 -192
11-196 11-197 11-198
11-199 11-200 11-201
11-202 11-203 11-204
11-205 11-206 11-207
11-208 11-209 11-210
11-211 11-212 11-213
11-214 11-215 11-216
11-220 11-221 11-222
11-223 11-224 11-225
11-226 11-227 11-228
11-229 11-230 11-231
11-232 11-233 11-234
11-235 11-236 11-237
11-238 11-239 11-240
11-244 11-245 11-246
11-247 11-248 11-249
11-250 11-251
In another embodiment, this invention provides a composition comprising a compound of formula II and a pharmaceutically acceptable carrier. One aspect of this invention relates to a method of inhibiting GSK-3 activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula II.
7Λnother aspect relates to a method of treating a disease that is alleviated by treatment with a GSK-3 inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula II.
Another aspect relates to a method of enhancing glycogen synthesis and/or lowering blood levels of - glucose in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula II. This method is especially useful for diabetic patients .
Another aspect relates to a method of inhibiting the production of hyperphosphorylated Tau protein in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula II. This method is especially useful in halting or slowing the progression of Alzheimer's disease.
Another aspect relates to a method of inhibiting the phosphorylation of β-catenin in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula II. This method is especially useful for treating schizophrenia.
One aspect of this invention relates to a method of inhibiting Aurora activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula II.
Another aspect relates to a method of treating a disease that is alleviated by treatment with an Aurora inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula II . This method is especially useful for treating cancer, such as colon, ovarian, and breast cancer.
One aspect of this invention relates to a method of inhibiting CDK-2 activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula II .
Another aspect relates to a method of treating a disease that is alleviated by treatment with a CDK-2 inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula II . This method is especially useful for treating cancer, Alzheimer's disease, restenosis, angiogenesis, glomerulonephritis, cytomegalovirus, HIV, herpes, psoriasis, atherosclerosis, alopecia, and autoimmune diseases such as rheumatoid arthritis .
Another method relates to inhibiting GSK-3, Aurora, or CDK-2 activity in a biological sample, which method comprises contacting the biological sample with the GSK-3 or Aurora inhibitor of formula II, or a pharmaceutical composition thereof, in an amount effective to inhibit GSK-3, Aurora or CDK-2. Each of the aforementioned methods directed to the inhibition of GSK-3, Aurora or CDK-2, or the treatment of a disease alleviated thereby, is preferably carried out with a preferred compound of formula II, as described above.
Another embodiment of this invention relates to compounds of formula III :
III or a pharmaceutically acceptable derivative or prodrug thereof, wherein: Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein Ring D is substituted at any substitutable ring carbon by oxo or -R5, and at any substitutable ring nitrogen by -R4, provided that when Ring D is a six-membered aryl or heteroaryl ring, -R5 is hydrogen at each ortho carbon position of Ring D; Rx and Ry are taken together with their intervening atoms to form a fused, benzo ring or a 5-8 membered carbocyclo ring, wherein any substitutable carbon on said fused ring formed by Rx and Ry is substituted by oxo or T-R3; T is a valence bond or a Cι_4 alkylidene chain; R2 and R2' are independently selected from -R, -T- -R6, or R2 and R2' are taken together with their intervening atoms to form a fused, 5-8 membered, unsaturated or partially unsaturated, ring having 0-3 ring heteroatoms selected from nitrogen, oxygen, or sulfur, wherein each substitutable carbon on said fused ring formed by R2 and R2' is substituted by halo, oxo, -CN, -N02, -R7, or -V-R6, and any substitutable nitrogen on said ring formed by R2 and R2' is substituted by R4; R3 is selected from -R, -halo, =0, -OR, -C(=0)R, -C02R, -COCOR, -COCH2COR, -N02, -CN, -S(0)R, -S(0)2R, -SR, -N(R4)2, -C0N(R4)2, -S02N(R)2, -OC(=0)R, -N(R4)COR, -N(R4) C02 (optionally substituted Cι-6 aliphatic) , -N(R4)N(R4)2, -C=NN(R4)2, -C=N-OR, -N (R4) CON (R4) 2, -N(R4)S02N(R4)2, -N(R4)S02R, or -OC (=0) N (R4) 2; each R is independently selected from hydrogen or an optionally substituted group selected from C_-6 aliphatic, C6-ιo aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms ; each R4 is independently selected from -R7, -COR7,
-C02 (optionally substituted Cχ-6 aliphatic) , -C0N(R7)2, or -S02R7, or two R4 on the same nitrogen are taken together to form a 5-8 membered heterocyclyl or heteroaryl ring; each R5 is independently selected from -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -CON(R4)2, -S02N(R4)2, -OC(=0)R, -N(R4)COR, -N(R4) C02 (optionally substituted C_s aliphatic) , -N(R4)N(R4)2, -C=NN(R4)2, -C=N-0R, -N (R4) CON (R4) _ , -N(R4)S02N(R4)2, -N(R4)S02R, or -OC (=0) N (R4) _ ; V is -0-, -S-, -SO-, -S02-, -N(Rs)S02-, -S02N(R6)-, -N(R6)-, -CO-, -CO2-, -N(R6)CO-, -N(R6)C(0)0-, -N(R6)C0N(R6) -, -N(R6)S02N(R6) -, -N (R6) N (R6) - , -C(0)N(R6)-, -OC(0)N(R6)-, -C(R6)20-, -C(R6)2S-, -C(R6)2S0-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C (Rε) 2N (R6) - , -C(R6)2N(R6)C(0)-, -C(Re)2N(R6)C(0)0-, -C (R6) =NN(R6) - , -C(R6)=N-0-, -C(R6)2N(R6)N(R6) -, -C (Re) 2N(R6) S02N (Re) - , or -C(R6)2N(R6)CON(R6)-; W is -C(R6)20-, -C(R6)2S-, -C(R6)2SO-, -C(R6)2S02-, -C(R6)2S02N(R6) -, -C(R6)2N(R6)-, -CO-, -C02-, -C(R6)OC(0) -, -C(R6)OC(0)N(R6) -, -C (R6) 2N(Re) CO- , -C(R6)2N(R6)C(0)0-, -C(R6)=NN(R6)-, -C(R6)=N-0-, -C(R6)2N(R6)N(Re)-, -C(R6)2N(Re)S02N(R6)-, -C(Re)2N(R6)CON(R6)■-, or -CON(R6)-; each R6 is independently selected from hydrogen or an optionally substituted Ci-4 aliphatic group, or two R6 groups on the same nitrogen atom are taken together with the nitrogen atom to form a 5-6 membered heterocyclyl or heteroaryl ring; and each R7 is independently selected from hydrogen or an optionally substituted Cι_6 aliphatic group, or two R7 on the same nitrogen are taken together with the nitrogen to form a 5-8 membered heterocyclyl or heteroaryl ring.
Preferred formula III Ring D monocyclic rings include substituted and unsubstituted phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, thienyl, azepanyl, and orpholinyl rings. When two adjacent substituents on Ring D are taken together to form a fused ring, the Ring D system is bicyclic. Preferred formula III Ring D bicyclic rings include 1,2,3,4- tetrahydroisoquinolinyl, 1, 2, 3 , 4-tetrahydroquinolinyl, 2, 3-dihydro-lff-isoindolyl, 2, 3 -dihydro-Iff-indolyl, isoquinolinyl, quinolinyl, and naphthyl. Examples of more preferred bicyclic Ring D systems include naphthyl and isoquinolinyl.
Preferred R5 substituents on Ring D of formula III include halo, oxo, CN, -N02, -N(R4)2, -C02R, -CONH(R4), -N(R)COR, -S02N(R4)2, -N(R4)S02R, -SR, -OR, -C(0)R, or substituted or unsubstituted group selected from 5-6 membered heterocyclyl, C6-ιo aryl, or Cι-6 aliphatic. More preferred R5 substituents include -halo, -CN, -oxo, -SR, -OR, -N(R4)2, -C(0)R, or a substituted or unsubstituted group selected from 5-6 membered heterocyclyl, C6-ι0 aryl, or Cι-6 aliphatic . Examples of Ring D substituents include -OH, phenyl, methyl, CH20H, CH2CH20H, pyrrolidinyl, OPh, CF3, C≡CH, Cl, Br, F, I, NH2, C(0)CH3, i-propyl, tert-butyl, SEt, OMe, N(Me)2, methylene dioxy, and ethylene dioxy.
Preferred rings formed when the Rx and Ry groups of formula III are taken together to form a fused ring include a 5-, 6-, or 7-membered unsaturated or partially unsaturated carbocyclo ring, wherein any substitutable carbon on said fused ring is substituted by oxo or T-R3. Examples of preferred bicyclic ring systems are shown below.
III - F III - I
Preferred substituents on the Rx/Rγ fused ring of formula III include -R, oxo, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -CON(R4)2, -S02N(R)2, -OC(=0)R, -N(R4)C0R," -N (R4) C02 (optionally substituted Cι-6 aliphatic) , -N(R4)N(R4) 2, -C=NN(R4)2, -C=N-OR, -N(R4)C0N(R4)2, -N (R4) S02N(R4) 2, -N(R4)S02R, or -0C(=0)N(R4) 2, wherein R and R4 are as defined above. More preferred substituents on the Rx/Rγ fused ring include halo, CN, oxo, Cα-6 alkyl, Cι-6 alkoxy, (Cι_6 alkyl) carbonyl, (C_.6 alkyl) sulfonyl, mono- or dialkylamino, mono- or dialkylaminocarbonyl, mono- or dialkylaminocarbonyloxy, or 5-6 membered heteroaryl.
Examples of such preferred substituents include methoxy, methyl, isopropyl, methylsulfonyl, cyano, chloro, pyrrolyl, methoxy, ethoxy, ethylamino, acetyl, and acetamido . Preferred R2 substituents of formula III include hydrogen, Cι_4 aliphatic, alkoxycarbonyl, (un) substituted phenyl, hydroxyalkyl, alkoxyalkyl, aminocarbonyl, mono- or dialkylaminocarbonyl, aminoalkyl, alkylaminoalkyl , dialkylaminoalkyl , phenylaminocarbonyl , and (N- heterocyclyl) carbonyl. Examples of such preferred R2 substituents include methyl, cyclopropyl, ethyl, isopropyl, propyl, t-butyl, cyclopentyl, phenyl, C02H, C02CH3, CH2OH, CH2OCH3, CH2CH2CH2OH, CH2CH2CH2OCH3 , CH2CH2CH2OCH2Ph, CH2CH2CH2NH2 , CH2CH2CH2NHCOOC (CH3) 3 , CONHCH(CH3)2, CONHCH2CH=CH2, CONHCH2CH2OCH3 , CONHCH2Ph, CONH (eyelohexyl) , CON(Et)2, CON(CH3) CH2Ph, CONH (n-C3H7) , CON(Et)CH2CH2CH3, CONHCH2CH (CH3) _ , CON (n-C3H7) 2, CO (3- methoxymethylpyrrolidin-1-yl) , CONH (3-tolyl) , CONH (4- tolyl) , CONHCH3, CO (morpholin-1-yl) ,' CO (4-methylpiperazin- 1-yl) , CONHCH2CH2OH, CONH2, and CO (piperidin-1-yl) .
When the R2 and R2' groups of formula III are taken together to form a ring, preferred R2/R2' ring systems containing the pyrazole ring include benzo, pyrido, pyrimido, 3-oxo-2ff-pyridazino, and a partially unsaturated 6-membered carbocyclo ring. Examples of such preferred R2/R2' ring systems containing the pyrazole ring include the following:
Preferred substituents on the R2/R2' fused ring of formula III include one or more of the following: -halo, -N(R4)2, -C3..4 alkyl, -Cι-4 haloalkyl, -N02, -0(Cι_4 alkyl), -C02 (Cι-4 alkyl) , -CN, -S02 (d-4 alkyl) , -S02NH2, -0C(0)NH2, -NH2S02(Cι_4 alkyl) , -NHC(O) (d-4 alkyl) , -C(0)NH2, ■ and -CO (d-4 alkyl) , wherein the (Cι-4 alkyl) is a straight, branched, or cyclic alkyl group. Preferably, the (C1- alkyl) group is methyl.
Preferred formula III compounds have one or more, and more preferably all, of the features selected from the group consisting of: (a) Ring D is an optionally substituted ring selected from a phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, thienyl, azepanyl, morpholinyl, 1, 2, 3, 4 -tetrahydroisoquinolinyl, 1,2,3,4- tetrahydroquinolinyl, 2, 3-dihydro-lff-isoindolyl, 2,3- dihydro-Iff- indolyl, isoquinolinyl, quinolinyl, or naphthyl ring;
(b) Rx and Ry are taken together with their intervening atoms to form an optionally substituted benzo ring or a 5-7 membered carbocyclo ring; and
(c) R2' is hydrogen or methyl and R2 is T-W-R6 or R, wherein W is -C(Re)20-, -C (R6) 2N(R6) - , -CO-, -C02-, -C(R6)OC(0) -, -C(Rβ)2N(R6)CO-, -C (R6) 2N(R6) C (O) O- , or -CON(R6)-, and R is an optionally substituted group selected from d-6 aliphatic or phenyl, or R2 and R2' are taken together with their intervening atoms to form a substituted or unsubstitutedbenzo, pyrido, pyrimido, or partially unsaturated 6-membered carbocyclo ring.
More preferred compounds of formula III have one or more, and more preferably all, of the features selected from the group consisting of:
(a) Ring D is an optionally substituted ring selected from phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, morpholinyl, 1,2,3,4- tetrahydroisoquinolinyl, 1, 2 , 3, 4-tetrahydroquinolinyl, 2, 3-dihydro-lff-isoindolyl, 2, 3 -dihydro-Iff-indolyl, isoquinolinyl, quinolinyl, or naphthyl;
(b) Rx and Ry are taken together with their intervening atoms to form a benzo ring or a 5-7 membered carbocyclo ring optionally substituted with -R, oxo-, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R )2, -CON(R4)2, -S02N(R4)2, -0C(=0)R, -N(R4)COR, -N(R4)C02 (optionally substituted Cχ-6 aliphatic) , -N (R ) N (R4 ) 2 , -C=NN (R ) 2 , -C=N-OR, -N (R4 ) CON (R4 ) _ , -N (R4 ) S02N (R4 ) 2 , -N (R4 ) S02R, or -OC ( =0) N (R4 ) _ ; and
(c) each R5 is independently selected from halo, oxo, CN, N02, -N(R4)2, -C02R, -CONH(R4), -N(R4)COR, -S02N(R4)2, -N(R4)S02R, -SR, -OR, -C(0)R, or a substituted or unsubstituted group selected from 5-6 membered heterocyclyl, C6-ιo aryl, or Cι-6 aliphatic.
Even more preferred compounds of formula III have one or more, and more preferably all, of the features selected from the group consisting of :
(a) Rx and Ry are taken together with their intervening atoms to form a benzo or 6-membered partially unsaturated carbocyclo ring optionally substituted with halo, CN, oxo, Cι-6 alkyl, 'd-6 alkoxy, (Cι_6 alkyl) carbonyl, ( -s alkyl) sulfonyl, mono- or dialkylamino, mono- or dialkylaminocarbonyl, mono- or dialkylaminocarbonyloxy, or 5-6 membered heteroaryl ,-
(b) each R5 is independently selected from -halo, -CN, -oxo, -SR, -OR, -N(R )2, -C(0)R, or a substituted or unsubstituted group selected from 5-6 membered heterocyclyl, C6-ιo aryl, or -6 aliphatic; and
(c) R2' is hydrogen and R2 is selected from R2' is hydrogen or methyl and R2 is T-W-R6 or R, wherein W is -C(R6)20-, -C(R6)2N(R6)-, -CO-, -C02-, -C (Re) OC (O) - , -C(R6)2N(R6)CO-, or -CON(R6)-, and R is an optionally substituted group selected from Cι_6 aliphatic or phenyl, or R2 and R2' are taken together with their intervening atoms to form a benzo, pyrido, or partially unsaturated 6-membered carbocyclo ring optionally substituted with -halo, -N(R4)2, -d-4 alkyl, -d-4 haloalkyl, -N02, -θ(d-4 alkyl), -C02 (d-4 alkyl) , -CN, -S02 (d-4 alkyl) , -S02NH2,' -OC(0)NH2, -NH2S02(d-4 alkyl) , -NHC(O) (d-4 alkyl) , -C(0)NH2, or -CO (Cχ.4 alkyl) , wherein the (d_4 alkyl) is a straight, branched, or cyclic alkyl group.
Representative compounds of formula III are set forth in Table 2 below.
Table 2
III-4 III-5 III-6
III-7 III-8 III-9
111-10 III-ll 111-12
111-13 111-14 111-15
111-16 111-17' 111-18
111-19 111-20 111-21
111-22 111-23 111-24
111-25 111-26 111-27
HN
. wto
111-28 111-29 111-30
111-31 111-32 111-33
111-34 111-35 111-36
111-37 111-38 111-39 ^Y
111-40 111-41 111-42
111-43 111-44 111-45
111-46 111-47 111-48
111-49 111-50 111-51
111-55 111-56 111-57
111-58 111-59 111-60
IIΪ-61 111-62 111-63
111-67 111-68 111-69
111-70 111-71 111-72
111-73 111-74 111-75
111-76 111-77 111-78
111-79 111-80 111-81 11-82 111-83 111-84
111-85 111-86 111-87
111-88 111-89 111-90
111-91 111-92 111-93
III.-94 111-95 111-96
H HNIM''V
111-97 111-98 111-99
III-100 III-101 III-102
III-103 III-104 III-105
III-106 III-107 III-108
III-109 III-110 III-lll
III-112 III-113 III-114
III-115 III-116 III-117
III-118 III-119 III-120
III-121 III-122 III-123
III-124 III-125 III-126
III-127 III-128 III-129
III-130 III-131 III-132
III-133 III-134 III-135 -136 III-137 III-138
III-139 III-140 III-141
-142 III-143 III-144
III-145 III-146 In another embodiment, this invention provides a composition comprising a compound of formula III and a pharmaceutically acceptable carrier.
One aspect of this invention relates to a method of inhibiting GSK-3 activity in a patient, comprising administering to the patient -a therapeutically effective amount of a composition comprising a compound of formula III .
Another aspect relates to a method of treating a disease that is alleviated by treatment with a GSK-3 inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula III . 7Another aspect relates to a method of enhancing glycogen synthesis and/or lowering blood levels of glucose in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula III. This method is especially useful for diabetic patients .
7Another aspect relates to a method of inhibiting the production of hyperphosphorylated Tau protein in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula III. This method is especially useful in halting or slowing the progression of Alzheimer's disease. Another aspect relates to a method of inhibiting the phosphorylation of β-catenin in a> patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula III. This method is especially useful for treating schizophrenia.
One aspect of this invention relates to a method of inhibiting Aurora activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula III.
Another aspect relates to a method of treating a disease that is alleviated by treatment with an Aurora inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula III . This method is especially useful for treating cancer, such as colon, ovarian, and breast cancer.
One aspect of this invention relates to a method of inhibiting CDK-2 activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula III.
Another aspect relates to a method of treating a disease that is alleviated by treatment with a CDK-2 inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula III. This method is especially useful for treating cancer, Alzheimer's disease, restenosis, angiogenesis, glomerulonephritis, cytomegalovirus, HIV, herpes, psoriasis, atherosclerosis, alopecia, and autoimmune diseases such as rheumatoid arthritis.
One aspect of this invention relates to a method of inhibiting Src activity in a patient, comprising administering to the patient a therapeutically effective amount, of a composition comprising a compound of formula III.
Another aspect relates to a method of treating 5. a disease that is alleviated by treatment with a Src inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula III. This method is 0 especially useful for treating hypercalcemia, osteoporosis, osteoarthritis, cancer, symptomatic treatment of bone metastasis, and Paget ' s disease.
Another method relates to inhibiting GSK-3, Aurora, CDK-2, or Src activity in a biological sample, 5 which method comprises contacting the biological sample with the GSK-3, Aurora, CDK-2, or Src inhibitor of formula III, or a pharmaceutical composition thereof, in an amount effective to inhibit GSK-3, Aurora, CDK-2, or Src. 0 Each of the aforementioned methods directed to the inhibition of GSK-3, Aurora, CDK-2, or Src, or the treatment of a disease alleviated thereby, is preferably carried out with a preferred compound of formula III, as described above. 5 Compounds of formula III, wherein R2' is hydrogen and Rx and Rγ are taken together with the pyrimidine ring to form an optionally substituted quinazoline ring system, are also inhibitors of ERK-2 and AKT protein kinases. 0 Accordingly, another method of this invention relates to a method of inhibiting ERK-2 or AKT activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula III, wherein R2' is hydrogen and Rx and Rγ are taken together with the pyrimidine ring to form an optionally substituted quinazoline ring system. Another aspect relates to a method of treating a disease that is alleviated by treatment with a ERK-2 or AKT inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula III, wherein R2' is hydrogen and Rx and Ry are taken together with the pyrimidine ring to form an optionally substituted quinazoline ring system. This method is especially useful for treating cancer, stroke, hepatomegaly, cardiovascular disease, Alzheimer's disease, cystic fibrosis, viral disease, autoimmune diseases, restenosis, psoriasis, allergic disorders including asthma, inflammation, and neurological disorders.
Another embodiment of this invention relates to compounds of formula IV:
IV or a pharmaceutically acceptable derivative or prodrug thereof, wherein: Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein Ring D is substituted at any substitutable ring carbon by oxo or -R5, and at any substitutable ring nitrogen by -R4, provided that when Ring D is a six-membered aryl or heteroaryl ring, -R5 is hydrogen at each ortho carbon position of Ring D; Rx and Ry are independently selected from T-R3, or Rx and Ry are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-8 membered ring having 1-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen, wherein any substitutable carbon on said fused ring is optionally and independently substituted by T-R3, and any substitutable nitrogen on said ring is substituted by
R4; T is a valence bond or a d-4 alkylidene chain; R2 and R2' are independently selected from -R, -T-W-R6, or R2 and R2' are taken together with their intervening atoms to form a fused, 5-8 membered, unsaturated or partially unsaturated, ring containing 0-3 ring heteroatoms selected from nitrogen, oxygen, or sulfur, wherein said fused ring is optionally substituted by up to three groups independently selected from halo, oxo, -CN, -N02, -R7, or -V-R6;
R3 is selected from -R, -halo, =0, -OR, -C(=0)R, -C02R, -COCOR, -C0CH2C0R, -N02, -CN, -S(0)R, -S(0)2R, -SR, -N(R4)2, -CON(R)2, -S02N(R4)2, -OC(=0)R, -N(R4)C0R, -N(R4) C02 (optionally substituted Cχ-6 aliphatic) , -N(R4)N(R4)2, -C=NN(R4)2, -C=N-OR, -N(R4) CON (R4) _ , -N(R4)S02N(R4)2, -N(R4)S02R, or -OC (=0) N (R4) 2; each R is independently selected from hydrogen or an optionally substituted group selected from Cι_6 aliphatic, C6-ιo aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms ; each R4 is independently selected from -R7, -COR7,
-C02 (optionally substituted C_-e aliphatic) , -C0N(R7)2, or -S02R7, or two R4 on the same nitrogen are taken together to form a 5-8 membered heterocyclyl or heteroaryl ring; each R5 is independently selected from -R,.halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R)2, -C0N(R4)2, -S02N(R4)2, -0C(=0)R, -N(R4)COR, -N(R4) C02 (optionally substituted Cι-6 aliphatic) , -N(R4)N(R4)2, -C=NN(R4)2, -C=N-0R, -N (R4) CON (R4) 2, -N(R4)S02N(R4)2, -N(R4)S02R, or -OC(=0)N(R4)2; V is -0-, -S-, -SO-, -S02-, -N(R6)S02-, -S02N(R6)-, -N(R6)-, -CO-, -CO2-, -N(R6)CO-, -N(R6)C(0)0-, -N(R6)CON(Re) -, -N(Re)S02N(Re) -, -N (Re) N(Re) - , -C(0)N(R6)-, -OC(0)N(R6)-, -C(Rs)20-, -C(R6)2S-,
-C(Rε)2SO-, -C(Rs)2S02-, -C(R6)2S02N(R6)-, -C (R6) 2N(R6) - , -C(R6)2N(R6)C(0) -, -C(R6)2N(Rs)C(0)0-, -C (R6) =NN (R6) - , -C(Rs)=N-0-, -C(R6)2N(R6)N(R6) -, -C (R6) 2N(R6) S02N(R6) - , or -C(R6)2N(R6)CON(R6) -; W is -C(Re)20-, -C(R6)2S-, -C(R6)2SO-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C(R6)2N(R6)-, -CO-, -C02-, -C(R6)0C(0) -, -C(R6)OC(0)N(R6) -, -C (R6) 2N(RS) CO- , -C(R6)2N(R6)C(0)0-, -C(R6)=NN(RS)-, -C(R6)=N-0-, -C(R6)2N(R6)N(R6) -, -C(R6)2N(Re)S02N(R6)-, -C(R6)2N(R6)CON(Re) -, or -CON(Rε)-; each R6 is independently selected from hydrogen or an optionally substituted C1-4 aliphatic group, or two Rs groups on the same nitrogen atom are taken together with the nitrogen atom to form a 5-6 membered heterocyclyl or heteroaryl ring; and each R7 is independently selected from hydrogen or an optionally substituted d-6 aliphatic group, or two R7 on the same nitrogen are taken together with the nitrogen to form a 5-8 membered heterocyclyl ring or heteroaryl .
Preferred formula IV Ring D monocyclic rings include substituted and unsubstituted phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, thienyl, azepanyl, and morpholinyl rings. Preferred formula IV Ring D bicyclic rings include 1,2,3,4- tetrahydroisoquinolinyl, 1,2,3, 4-tetrahydroquinolinyl , 2, 3-dihydro-lH-isoindolyl, 2, 3 -dihydro-lJJ-indolyl, isoquinolinyl, quinolinyl, and naphthyl. Examples of more preferred Ring D bicyclic rings include naphthyl and isoquinolinyl .
Preferred substituents on Ring D of formula IV include halo, oxo, CN, -N02, -N(R4)2, -C02R, -CONH(R4), -N(R4)COR, -S02N(R4)2, -N(R4)S02R, -SR, -OR, -C(0)R, or substituted or unsubstituted group selected from 5-6 membered heterocyclyl, C6-ιo aryl, or d-6 aliphatic. More preferred R5 substituents include -halo, -CN, -oxo, -SR, -OR, -N(R4)2, -C(0)R, or a substituted or unsubstituted group selected from 5-6 membered heterocyclyl, C6-ιo aryl, or Cι-6 aliphatic. Examples of Ring D substituents include -OH, phenyl, methyl, CH2OH, CH2CH2OH, pyrrolidinyl, OPh, CF3, C≡CH, Cl, Br, F, I, NH2, C(0)CH3, i-propyl, tert-butyl, SEt, OMe, N(Me)2, methylene dioxy, and ethylene dioxy.
When the Rx and Rγ groups of formula IV are taken together to form a fused ring, preferred Rx/Rγ rings include a 5-, 6-, 7-, or 8-membered unsaturated or partially unsaturated ring having 1-2 heteroatoms. This provides a bicyclic ring system containing the pyrimidine ring. Examples of preferred pyrimidine ring systems of formula IV are the mono- and bicyclic systems shown below.
IV-D IV-E IV-G
IV-H IV-J IV-K
IV- IV-M IV-N
IV-ϋ IV-V IV-W
IV-DD
More preferred pyrimidine ring systems of formula IV include IV-E, IV-G, IV-H, IV-J, IV-K, IV-L, IV-M, IV-T, and IV-U.
In the monocyclic pyrimidine ring system of formula IV, preferred Rx groups include hydrogen, amino, nitro, alkyl- or dialkylamino, acetamido, or a Cι-4 aliphatic group such as methyl, ethyl, cyclopropyl, isopropyl or t-butyl. Preferred Rγ groups include T-R3 wherein T is a valence bond or a methylene, and R3 is -R, -N(R4)2, or -OR. When R3 is -R or -OR, a preferred R is an optionally substituted group selected from Cι-6 aliphatic, phenyl, or a 5-6 membered heteroaryl or heterocyclyl ring. Examples of preferred Rγ groups include 2-pyridyl, 4-pyridyl, piperidinyl, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, alkyl- or dialkylamino, acetamido, optionally substituted phenyl such as phenyl, methoxyphenyl , trimethoxyphenyl , or halo-substituted phenyl , and methoxymethyl . In the bicyclic pyrimidine ring system of formula IV, the ring formed when Rx and Ry are taken together may be substituted or unsubstituted. Suitable substituents include -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R)2, -C0N(R4)2, -S02N(R4)2, -OC(=0)R, -N(R)C0R, -N (R4) C02 (optionally substituted d_6 aliphatic) , -N(R4)N(R4)2, -C=NN(R4)2, -C=N-OR, -N(R)C0N(R4)2, -N(R4) S02N (R4) 2, -N(R)S02R, or -0C(=0)N(R4)2, wherein R and R4 are as defined above for compounds of formula IV. Preferred Rx/Rγ ring substituents include -halo, -R, -OR, -COR, -C02R,
-C0N(R)2, -CN, or -N(R4)2 wherein R is a substituted or unsubstituted Cι-6 aliphatic group.
The R2 and R2' groups of formula IV may be taken together to form a fused ring, thus providing a bicyclic ring system containing a pyrazole ring. Preferred fused rings include benzo, pyrido, pyrimido, and a partially unsaturated 6-membered carbocyclo ring. These are exemplified in the following formula IV compounds having a pyrazole-containing bicyclic ring system:
Preferred substituents on the R2/R2' fused ring of formula IV include one or more of the following: -halo, -N(R4)2, -Cι-4 alkyl, -Cι_4 haloalkyl, -N02, -0(Cι-4 alkyl), -C02 (Cι.4 alkyl) , -CN, -S02 (Cι-4 alkyl) , -S02NH2, -OC(0)NH2, -NH2S02 (Ci-4 alkyl) , -NHC(O) (d-4 alkyl) , -C(0)NH2, and -CO (C1-4 alkyl) , wherein the (Cι.4 alkyl) is a straight, branched, or cyclic alkyl group. Preferably, the (Ci-4 alkyl) group is methyl.
When the pyrazole ring system of formula IV is monocyclic, preferred R2 groups include hydrogen, a substituted or unsubstituted group selected from aryl, heteroaryl, or a d-6 aliphatic group. Examples of such preferred R2 groups include methyl, t-butyl, -CH20CH3, cyclopropyl, furanyl, thienyl, and phenyl. A preferred R2' group is hydrogen.
Preferred formula IV compounds have one or more, and more preferably all, of the features selected from the group consisting of:
(a) Ring D is an optionally substituted ring selected from a phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, thienyl, azepanyl, morpholinyl, 1, 2, 3 , 4-tetrahydroisoquinolinyl, 1,2,3,4- tetrahydroquinolinyl, 2 , 3-dihydro-lH-isoindolyl, 2,3- dihydro-lJf-indolyl, isoquinolinyl, quinolinyl, or naphthyl ring; (b) Rx is hydrogen or Cι-4 aliphatic and Rγ is T- R3, or Rx and Rγ are taken together with their intervening atoms to form an optionally substituted 5-7. membered unsaturated or partially unsaturated ring having 1-2 ring heteroatoms ; and
(c) R2' is hydrogen or methyl and R2 is T-W-Rs or R, wherein W is -C(R6)20-, -C (R6) 2N(Re) - , -CO-, -C02-, -C(Re)0C(0) -, -C(R6)2N(R6)CO-, -C (Re) 2N (R6) C (O) O- , or -CON(Rs)-, and R is an optionally substituted group selected from d-6 aliphatic or phenyl, or R2 and R2' are taken together with their intervening atoms to form a substituted or unsubstituted benzo, pyrido, pyrimido, or partially unsaturated 6-membered carbocyclo ring.
More preferred compounds of formula IV have one or more, and more preferably all, of the features selected from the group consisting of:
(a) Ring D is an optionally substituted ring selected from phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, morpholinyl, 1,2,3,4- tetrahydroisoquinolinyl, 1, 2, 3, 4-tetrahydroquinolinyl, 2, 3-dihydro-lH-isoindolyl, 2, 3 -dihydro-lH-indolyl, isoquinolinyl, quinolinyl, or naphthyl;
(b) Rx is hydrogen or methyl and Ry is -R, N(R4)2, or -OR, or R and Rγ are taken together with their intervening atoms to form a 5-7 membered unsaturated or partially unsaturated ring having 1-2 ring nitrogens, wherein said ring is optionally substituted with -R, halo, oxo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -CON(R4)2, -S02N(R4)2, -OC(=0)R, -N(R4)COR, -N(R4) C02 (optionally substituted d-6 aliphatic) , -N(R4)N(R4)2, -C=NN(R )2, -C=N-0R, -N(R4) CON (R4) 2, -N(R4)S02N(R4)2, -N(R4)S02R, or -OC (=0)N(R4) 2; and (c) each R5 is independently selected from halo, oxo, CN, N02, -N(R4)2, -C02R, -CONH(R4), -N(R4)COR, -S02N(R4)2, -N(R4)S02R, -SR, -OR, -C(0)R, or a substituted or unsubstituted group selected from 5-6 membered heterocyclyl, C6-ιo aryl, or Cι-6 aliphatic.
Even more preferred compounds of formula IV have one or more, and more preferably all, of the features selected from the group consisting of:
(a) Rx and Ry are taken together with their intervening atoms to form a 6-membered unsaturated or partially unsaturated ring having 1-2 ring nitrogens, optionally substituted with halo, CN, oxo, Cχ-6 alkyl, Cι_s alkoxy, (Cι-6 alkyl) carbonyl, (Cι_ε alkyl) sulfonyl, mono- or dialkylamino, mono- or dialkylaminocarbonyl, mono- or dialkylaminocarbonyloxy, or 5-6 membered heteroaryl;
(b) each R5 is independently selected from -halo, -CN, -oxo, -SR, -OR, -N(R4)2, -C(0)R, or a substituted or unsubstituted group selected from 5-6 membered heterocyclyl, Ce_ι0 aryl, or d-e aliphatic; and (c) R2' is hydrogen and R2 is T-W-R6 or R, wherein W is -C(R6)20-, -C (R6) 2N(R6) - , -CO-, -C02-, -C(R6)OC(0) -, -C(R6)2N(R6)C0-, or -C0N(R6)-, and R is an optionally substituted group selected from Cι-6 aliphatic or phenyl, or R2 and R2' are taken together with their intervening atoms to form a benzo, pyrido, or partially unsaturated 6-membered carbocyclo ring optionally substituted with -halo, oxo, -N(R4)2, -d-4 alkyl, -Cι_4 haloalkyl, -N02, -O (d-4 alkyl) , -C02 (d-4 alkyl) , -CN, -S02 ( -4 alkyl) , -S02NH2, -0C(0)NH2, -NH2S02 (d-4 alkyl) , -NHC(O) (Ci-4 alkyl) , -C(0)NH2, or -CO (Cι-4 alkyl) , wherein the (Ci-4 alkyl) is a straight, branched, or cyclic alkyl group . Representative compounds of formula IV are set forth in Table 3 below .
Table 3 .
IV- 1 IV- 2 IV- 3'
IV-4 IV- 5 IV- 6
IV- 7 IV- 8 IV- 9
IV-10 IV-11 IV-12
IV- 13 IV- 14 IV-15
IV- 16 IV- 17 IV- 18
IV- 19 IV- 20 IV- 21
IV- 22 IV- 23 IV- 24
IV- 25 IV- 26 IV- 27
IV- 28 IV- 29 IV- 30
J.V-31 IV-32 IV- 33
In another embodiment, this invention provides a composition comprising a compound of formula IV and a pharmaceutically acceptable carrier.
One aspect of this invention relates to a method of inhibiting GSK-3 activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula IV.
Another aspect relates to a method of treating a disease that is alleviated by treatment with a GSK-3 inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula IV.
Another aspect relates to a method of enhancing glycogen synthesis and/or lowering blood levels of glucose in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula IV. This method is especially useful for diabetic patients. Another aspect relates to a method of inhibiting the production of hyperphosphorylated Tau protein in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula IV. This method is especially useful in halting or slowing the progression of Alzheimer's disease. Another aspect relates to a method of inhibiting the phosphorylation of β-catenin in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula IV. This method is especially useful for treating schizophrenia.
One aspect of this invention relates to a method of inhibiting Aurora activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula IV.
Another aspect relates to a method of treating a disease that is alleviated by treatment with an Aurora inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula IV. This method is especially useful for treating cancer, such as colon, ovarian, and breast cancer.
One aspect of this invention relates to a method of inhibiting CDK-2 activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula IV.
Another aspect relates to a method of treating a disease that is alleviated by treatment with a CDK-2 inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula IV. This method is especially useful for treating cancer, Alzheimer's disease, restenosis, angiogenesis, glomerulonephritis, cytomegalovirus-, HIV, herpes, psoriasis, atherosclerosis, alopecia, and autoimmune diseases such as rheumatoid arthritis .
Another method relates to inhibiting GSK-3, Aurora, or CDK-2 activity in a biological sample, which method comprises contacting the biological sample with the GSK-3 or Aurora inhibitor of formula IV, or a pharmaceutical composition thereof, in an amount effective to inhibit GSK-3, Aurora or CDK-2. Each of the aforementioned methods directed to the inhibition of GSK-3, Aurora or CDK-2, or the treatment of a disease alleviated thereby, is preferably carried out with a preferred compound of formula IV, as described above. Another embodiment of this invention relates to compounds of formula V:
V
or a pharmaceutically acceptable derivative or prodrug thereof, wherein:
Z1 is N, CRa, or CH and Z2 is N or CH, provided that one of Z1 and Z2 is nitrogen;
G is Ring C or Ring D;
Ring C is selected from a phenyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, or 1, 2, 4-triazinyl ring, wherein said Ring C has one or two ortho substituents independently selected from -R1, any substitutable non- ortho carbon position on Ring C is independently substituted by -R5, and two adjacent substituents on Ring C are optionally taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-6 membered ring having 0-3 heteroatoms selected from oxygen, sulfur or nitrogen, said fused ring being optionally substituted by halo, oxo, or -R8;
Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein Ring D is substituted at any substitutable ring carbon by oxo or -R5, and at any substitutable ring nitrogen by -R4, provided that when Ring D is a si -membered aryl or heteroaryl ring, -R5 is hydrogen at each ortho carbon position of Ring D;
R1 is selected from -halo, -CN, -N02, T-V-R6, phenyl, 5-6 membered heteroaryl ring, 5-6 membered heterocyclyl ring, or d-6 aliphatic group, said phenyl, heteroaryl, and heterocyclyl rings each optionally substituted by up to three groups independently selected from halo, oxo, or -R8, said Cι_s aliphatic group optionally substituted with halo, cyano, nitro, or oxygen, or R1 and an adjacent substituent taken together with their intervening atoms form said ring fused to Ring C;
Rx and Rγ are independently selected from T-R3, or Rx and Ry are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-8 membered ring having 0-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen, wherein any substitutable carbon on said fused ring formed by Rx and Ry is substituted by oxo or T-R3, and any substitutable nitrogen on said ring formed by Rx and Ry is substituted by R4;
T is a valence bond or a Cι_4 alkylidene chain;
R2 and R2' are independently selected from -R, -T-W-R6, or R2 and R2' are taken together with their intervening atoms to form a fused, 5-8 membered, unsaturated or partially unsaturated, ring having 0-3 ring heteroatoms selected from nitrogen, oxygen, or sulfur, wherein each substitutable carbon on said fused ring formed by R2 and R2' is substituted by halo, oxo, -CN, -N02, -R7, or -V-R6, and any substitutable nitrogen on said ring formed by R2 and R2' is substituted by R4;
R3 is selected from -R, -halo, -OR, -C(=0)R, -C02R, -COCOR, -COCH2COR, -N02, -CN, -S(0)R, -S(0)2R, -SR, -N(R4)2, -CON(R7)2, -S02N(R7)2, -0C(=0)R, -N(R7)COR, -N(R7) C02 (optionally substituted Cι-6 aliphatic) , -N(R4)N(R4)2, -C=NN(R)2, -C=N-0R, -N(R7) CON (R7) 2, -N(R7)S02N(R7)2, -N(R)S02R, or -OC (=0) N(R7) 2 ; each R is independently selected from hydrogen or an optionally substituted group selected from d-6 aliphatic, C6-10 aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms ; each R4 is independently selected from -R7, -COR7,
-C02 (optionally substituted d_6 aliphatic) , -CON(R7)2, or -S02R7, or two R4 on the same nitrogen are taken together to form a 5-8 membered heterocyclyl or heteroaryl ring; each R5 is independently selected from -R, halo, -OR, - -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -C0N(R4)2, -S02N(R)2, -OC(=0)R, -N(R4)COR, -N(R4) C02 (optionally substituted Cι-6 aliphatic) , . -N(R4)N(R4)2, -C=NN(R4)2, -C=N-0R, -N (R4) CON (R4) 2,
-N(R4)S02N(R4)2, -N(R4)S02R, or -OC (=0) N(R4) 2, or R5 and an adjacent substituent taken together with their intervening atoms form said ring fused to Ring C; V is -0-, -S-, -SO-, -S02-, -N(R6)S02-, -S02N(R6)-, -N(R6)-, -CO-, -C02-, -N(R6)CO-, -N (R6) C (O) O- , -N(R6)CON(R6) -, -N(R6)S02N(R6) -, -N(R6) N(R6) - , -C(0)N(R6)-, -OC(0)N(R6) -, -C(R6)20-, -C(R6)2S-, -C(R6)2S0-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C (R6) 2N (R6) - , -C(R6)2N(R6)C(0) -, -C(R6)2N(Rs)C(0)0-, -C (R6) =NN (R6) - , -C(R6)=N-0-, -C(Re)2N(Rs)N(R6) -, -C (R6) 2N (R6) S02N (R6) - , or -C(R6)2N(R6)CON(R6)-; W is -C(R6)20-, -C(R6)2S-, -C(R6)2SO-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C(R6)2N(R6)-, -CO-, -C02-, -C(R6)OC(0)-, -C(R6)OC(0)N(R6) -, -C (R6) 2N(R6) CO- , -C(R6)2N(R6)C(0)0-, -C (R6) =NN(R6) - , -C(R6)=N-0-, -C (R6) 2N (R6) N (R6) - , -C (R6) 2N (R6) S02N (R6) - , -C(R6)2N(R6)CON(R6)-, or -CON(Re)-; each R6 is independently selected from hydrogen, an optionally substituted C1-4 aliphatic group, or two R6 groups on the same nitrogen atom are taken together with the nitrogen atom to form a 5-6 membered heterocyclyl or heteroaryl ring; each R7 is independently selected from hydrogen or an optionally substituted Cι-6 aliphatic group, or two R7 on the same nitrogen are taken together with the nitrogen to form a 5-8 membered heterocyclyl or heteroaryl ring; each R8 is independently selected from an optionally substituted d-4 aliphatic group, -OR6, -SRS, -COR6, -S02R6, -N(R6)2, -N(R6)N(R6)2, -CN, -N02, -CON(R6)2, or -C02R6; and Ra is selected from halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -CON(R4)2, -S02N(R4)2, -OC(=0)R, -N(R4)COR, -N(R4) C02 (optionally substituted d-β aliphatic) , -N(R4) N(R4) _ , -C=NN(R4)2, -C=N-OR, -N(R4)CON(R4)2, -N(R4) S02N (R4) 2, -N(R )S02R, -0C(=0)N(R4) 2, or an optionally substituted group selected from d_6 aliphatic, C6-ιo aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms.
Compounds of formula V may be represented by specifying Z1 and Z2 as shown below:
Va Vb Vc
When the Rx and Rγ groups of formula V are taken together to form a fused ring, preferred Rx/Ry rings include a 5-, 6-, 7-, or 8-membered unsaturated or partially unsaturated ring having 0-2 heteroatoms, wherein said Rx/Ry ring is optionally substituted. This provides a bicyclic ring system containing a pyridine ring. Examples of preferred bicyclic ring systems of formula V are shown below.
Va-E Vb-E Vc-E
More preferred bicyclic ring systems of formula V include Va-A, Vb-A, Vc-A, Va-B, Vb-B, Vc-B, Va-D, Vb-D, Vc-D, Va-E, Vb-E, Vc-E, Va-J, Vb-J, Vc-J, Va-K, Vb-K, Vc-K, Va-L, Vb-L, Vc-L, Va-M, Vb-M, and Vc-M, most preferably Va-A, Vb-A, Vc-A, Va-B, Vb-B, and Vc-B. In the monocyclic pyridine ring system of formula V, preferred Rx groups include hydrogen, alkyl- or dialkylamino, acetamido, or a Cι-4 aliphatic group such as methyl, ethyl, cyclopropyl, isopropyl or t-butyl. Preferred Rγ groups include T-R3 wherein T is a valence bond or a methylene, and R3 is -R, -N(R)2, or -OR. When R3 is -R or -OR, a preferred R is an optionally substituted group selected from d-6 aliphatic, phenyl, or a 5-6 membered heteroaryl or heterocyclyl ring. Examples of preferred Rγ include 2-pyridyl, 4-pyridyl, piperidinyl, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, alkyl- or dialkylamino, acetamido, optionally substituted phenyl such as phenyl or halo-substituted phenyl, and methoxymethyl .
In the bicyclic ring system of formula V, the ring formed when Rx and Ry are taken together may be substituted or unsubstituted. Suitable substituents include -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -CON(R)2, -S02N(R4)2, -OC(=0)R, -N(R4)COR, -N(R)C02 (optionally substituted d_6 aliphatic), -N(R)N(R4) 2/ -C=NN(R4)2, -C=N-OR, -N(R4)CON(R4)2, -N(R4)S02N(R4)2, -N(R)S02R, or -OC(=0)N(R4) 2 , wherein R and R4 are as defined above. Preferred Rx/Rγ ring substituents include -halo, -R, -OR, -COR, -C02R, -CON(R4)2, -CN, or -N(R4)2 wherein R is an optionally substituted Cι-6 aliphatic group.
The R2 and R2' groups of formula V may be taken together to form a fused ring, thus providing a bicyclic ring system containing a pyrazole ring. Preferred fused rings include benzo, pyrido, pyrimido, and a partially unsaturated 6-membered carbocyclo ring. These are exemplified in the following formula V compounds having a pyrazole-containing bicyclic ring system:
Preferred substituents on the R2/R2' fused ring of formula V include one or more of the following: -halo, -N(R4)2, -Ci-4 alkyl, -d-4 haloalkyl, -N0 , -0 (Cι-4 alkyl) , -C02(Ci-4 alkyl) , -CN, -S02 (d-4 alkyl) , -S02NH2, -0C(0)NH2, -NH2S02(Ci-4 alkyl) , -NHC(O) (d-4 alkyl) , -C(0)NH2, and -CO (Ci-4 alkyl) , wherein the (d-4 alkyl) is a straight, branched, or cyclic alkyl group. Preferably, the (Cι_4 alkyl) group is methyl.
When the pyrazole ring system is monocyclic, preferred R2 groups include hydrogen, d-4 aliphatic, alkoxycarbonyl, (un) substituted phenyl, hydroxyalkyl, alkoxyalkyl, aminocarbonyl, mono- or dialkylaminocarbonyl, aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl , phenylaminocarbonyl, and (N- heterocyclyl) carbonyl. Examples of such preferred R2 substituents include methyl, cyclopropyl, ethyl, isopropyl, propyl, t-butyl, cyclopentyl, phenyl, C02H, C02CH3, CH2OH, CH2OCH3, CH2CH2CH2OH, CH2CH2CH2OCH3 , CH2CH2CH2OCH2Ph, CH2CH2CH2NH2, CH2CH2CH2NHCOOC (CH3) 3 ,
CONHCH(CH3)2, CONHCH2CH=CH2 , CONHCH2CH2OCH3, C0NHCH2Ph, CONH(cyclohexyl) , C0N(Et)2, CON(CH3) CH2Ph, CONH (n-C3H7) , CON(Et)CH2CH2CH3, CONHCH2CH (CH3) i , CON (n-C3H7) 2, CO (3- methoxymethylpyrrolidin-1-yl) , CONH (3-tolyl) , CONH (4- tolyl), CONHCH3, CO(morpholin-l-yl) , CO (4-methylpiperazin- 1-yl) , CONHCH2CH2OH, CONH2, and CO (piperidin-1-yl) . A preferred R2' group is hydrogen.
More preferred ring systems of formula V are the following, which may be substituted as described above, wherein R2 and R2' are taken together with the pyrazole ring to form an optionally substituted indazole ring; and Rx and Rγ are each methyl, or Rx and Rγ are taken together with the pyridine ring to form an optionally substituted quinoline, isoquinoline, tetrahydroquinoline or tetrahydroisoquinoline ring:
V-Aa V-Ba V-Ha
When G is Ring C, preferred formula V Ring C groups are phenyl and pyridinyl. When two adjacent substituents on Ring C are taken together to form a fused ring, Ring C is contained in a bicyclic ring system. Preferred fused rings include a benzo or pyrido ring. Such rings preferably are fused at ortho and meta positions of Ring C. Examples of preferred bicyclic Ring C systems include naphthyl and isoquinolinyl . Preferred R1 groups include -halo, an optionally substituted d-6 aliphatic group, phenyl, -COR6, -OR6, -CN, -S02R6, -S02NH2, -N(R6)2, -C02R6, -CONH2, -NHCOR6, -OC(0)NH2, or -NHS02R6. When R1 is an optionally substituted d_6 aliphatic group, the most preferred optional substituents are halogen. Examples of preferred R1 groups include -CF3, -Cl, -F, -CN, -COCH3, -OCH3, -OH, -CH2CH3, -OCH2CH3, -CH3, -CF2CH3, cyclohexyl, t-butyl, isopropyl, cyclopropyl, -C≡CH, -C≡C-CH3, -S02CH3, -S02NH2, -N(CH3)2, -C02CH3, -CONH2, -NHCOCH3, -OC(0)NH2, -NHS02CH3, and -OCF3.
On Ring C preferred R5 substituents, when present, include -halo, -CN, -N02, -N(R4)2, optionally substituted Cι-6 aliphatic group, -OR, -C(0)R, -C02R, -CONH(R4), -N(R4)C0R, -S02N(R4)2, and -N(R4) S02R. More preferred R5 substituents include -Cl, -F, -CN, -CF3, -NH2, - H(Ci-4 aliphatic), ~N(Cι-4 aliphatic)2, -0(d-4 aliphatic), Cι- aliphatic, and -C02(Cι_4 aliphatic).
Examples of such preferred R5 substituents include -Cl, -F, -CN, -CF3, -NH2, -NHMe, -NMe2, -OEt, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, and -C02Et.
When G is Ring D, preferred formula V Ring D monocyclic rings include substituted and unsubstituted phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, thienyl, azepanyl, and morpholinyl rings. When two adjacent substituents on Ring D are taken together to form a fused ring, the Ring D system is bicyclic. Preferred formula V Ring D bicyclic rings include 1, 2 , 3 , 4-tetrahydroisoquinolinyl, 1,2,3,4- tetrahydroquinolinyl, 2 , 3-dihydro-lH-isoindolyl, 2,3- dihydro-lH-indolyl, isoquinolinyl, quinolinyl, and naphthyl. Examples of more preferred bicyclic Ring D systems include naphthyl and isoquinolinyl .
Preferred substituents on Ring D of formula V include one or more of the following: halo, oxo, CN, -N02, -N(R4)2, -C02R, -CONH(R4), -N(R4)C0R, -S02N(R4)2, -N(R4)S02R, -SR, -OR, -C(0)R, or substituted or unsubstituted group selected from 5-6 membered heterocyclyl, C6-ιo aryl, or d-6 aliphatic . More preferred Ring D substituents include -halo, -CN, -oxo, -SR, -OR, -N(R4)2, -C(0)R, or a substituted or unsubstituted group selected from 5-6 membered heterocyclyl, C6-ι0 aryl, or _s aliphatic. Examples of Ring D substituents include -OH, phenyl, methyl, CH2OH, CH2CH2OH, pyrrolidinyl, OPh, CF3, G≡CH, Cl, Br, F, I, NH2, C(0)CH3, i-propyl, tert-butyl, SEt, OMe, N(Me)2, methylene dioxy, and ethylene dioxy.
Preferred formula V compounds have one or more, and more preferably all, of the features selected from the group consisting of :
(a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is selected from a naphthyl, quinolinyl or isoquinolinyl ring, and R1 is -halo, an optionally substituted Cι-6 aliphatic group, phenyl, -COR6, -OR6, -CN, -S02Re, -S02NH2, -N(R6)2, -C02R6, -CONH2, -NHCOR6, -OC(0)NH2, or -NHS02R6; or Ring D is an optionally substituted ring selected from a phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, thienyl, azepanyl , morpholinyl , 1,2,3,4- tetrahydroisoquinolinyl , 1,2,3, 4-tetrahydroquinolinyl, 2 , 3 -dihydro-Iff-isoindolyl, 2 , 3-dihydro- 1H-indolyl, isoquinolinyl, quinolinyl, or naphthyl ring; (b) Rx is hydrogen or Cι_4 aliphatic and Ry is T- R3, or Rx and Ry are taken together with their intervening atoms to form an optionally substituted 5-7 membered unsaturated or partially unsaturated ring having 0-2 ring nitrogens; and
(c) R2' is hydrogen and R2 is hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a d_6 aliphatic group, or R2 and R2' are taken together with their intervening atoms to form a substituted or unsubstituted benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring.
More preferred compounds of formula V have one or more, and more preferably all, of the features selected from the group consisting of: (a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is a naphthyl ring, and R1 is -halo, a Cι-6 haloaliphatic group, a d-6 aliphatic group, phenyl, or -CN; or Ring D is an optionally substituted ring selected from phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, morpholinyl, 1,2,3,4-tetrahydroisoquinolinyl , 1,2,3,4- tetrahydroquinolinyl, 2 , 3 -dihydro-lH-isoindolyl, 2,3- dihydro - 1H-indolyl, isoquinolinyl, quinolinyl, or naphthyl ;
(b) Rx is hydrogen or methyl and Ry is -R, N(R4)2, or -OR, or Rx and Rγ are taken together with their intervening atoms to form a benzo ring or a 5-7 membered partially unsaturated carbocyclo ring, said benzo or carbocyclo ring optionally substituted with -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -C0N(R4)2/ -S02N(R)2, -OC(=0)R, -N(R4)COR, -N(R4) C02 (optionally substituted C_.6 aliphatic) , -N(R4)N(R4)2, -C=NN(R4)2, -C=N-OR, -N (R4) C0N(R4) 2, -N(R4)S02N(R4)2, -N(R4)S02R, or -OC (=0)N(R4) 2;
(c) R2' is hydrogen and R2 is hydrogen or a substituted or unsubstituted group selected from aryl, or a d-6 aliphatic group, or R2 and R2' are taken together with their intervening atoms to form a substituted or unsubstituted benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring,- and (d) Ring D is substituted by oxo or R5, wherein each R5 is independently selected from -halo, -CN, -N02, -N(R)2, optionally substituted Cι-S aliphatic group, -OR, -C(0)R, -C02R, -CONH(R4), -N(R4)COR, -S02N(R4)2, or -N(R)S02R. Even more preferred compounds of formula V have one or more, and more preferably all, of the features selected from the group consisting of .-
(a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is a naphthyl ring, and R1 is -halo, a Cι-4 aliphatic group optionally substituted with halogen, or -CN; or Ring D is an optionally substituted ring selected from phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, morpholinyl, 1,2,3, 4-tetrahydroisoquinolinyl, 1,2,3,4- tetrahydroquinolinyl, isoquinolinyl, quinolinyl, or naphthyl;
(b) Rx is hydrogen or methyl and Ry is methyl, ethoxymethyl , ethyl, cyclopropyl, isopropyl, t-butyl, alkyl- or an optionally substituted group selected from 2-pyridyl, 4-pyridyl, piperidinyl, or phenyl, or Rx and Rγ are taken together with their intervening atoms to form a benzo ring or a 6-membered partially unsaturated carbocyclo ring optionally substituted with halo, CN, oxo, Cχ-6 alkyl, d_6 alkoxy, (Cι-6 alkyl) carbonyl, (Cι-6 alkyl) sulfonyl, mono- or dialkylamino, mono- or 5 dialkylaminocarbonyl, mono- or dialkylaminocarbonyloxy, or 5-6 membered heteroaryl;
(c) R2 and R2' are taken together with their intervening atoms to form a benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring
10. optionally substituted with -halo, -N(R4) , -d-4 alkyl,
-d-4 haloalkyl, -N02, -O (d-4 alkyl) , -C02 (d-4 alkyl) , -CN, -S02 (d-4 alkyl) , -S02NH2, -OC(0)NH2, -NH2S02 (d-4 alkyl) , -NHC(O) (d-4 alkyl) , -C(0)NH2, or -CO (d-4 alkyl) , wherein the (Cι_4 alkyl) is a straight, branched, or cyclic alkyl'
15 group; and
(d) Ring D is substituted by oxo or R5, wherein each R5 is independently selected from -Cl, -F, -CN, -CF3, -NH2, -NH(Cι_4 aliphatic), -N(Cι_4 aliphatic)2, -0(Cι-4 aliphatic), Ci-4 aliphatic, and -C02(d-4 aliphatic).
20 Representative compounds of formula V are set forth in Table 4 below.
Table 4 .
V-4 V-5 V-6
V-7 V-8 V-9
V- 64 V- 65 V- 66
In another embodiment, this invention provides a composition comprising a compound of formula V and a pharmaceutically acceptable carrier. One aspect of this invention relates to a method of inhibiting GSK-3 activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula V. Another aspect relates to a method of treating a disease that is alleviated by treatment with a GSK-3 inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula V.
Another aspect relates to a method of enhancing glycogen synthesis and/or lowering blood levels of glucose in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comorisincr a compound of formula V. This method is especially useful for diabetic patients .
Another aspect relates to a method of inhibiting the production of hyperphosphorylated Tau protein in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula V. This method is especially useful in halting or slowing the progression of Alzheimer's disease. Another aspect relates to a method of inhibiting the phosphorylation of β-catenin in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula V. This method is especially useful for treating schizophrenia.
One aspect of this invention relates to a method of inhibiting Aurora activity in a patient, comprising administering to the.patient a therapeutically effective amount of a composition comprising a compound of formula V.
Another aspect relates to a method of treating a disease that is alleviated by treatment with an Aurora inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula V. This method is especially useful for treating cancer, such as colon, ovarian, and breast cancer.
One aspect of this invention relates to a method of inhibiting CDK-2 activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula V. Another aspect relates to a method of treating a disease that is alleviated by treatment with a CDK-2 inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula V. This method is especially useful for treating cancer, Alzheimer's disease, restenosis, angiogenesis, glomerulonephritis, cytomegalovirus, HIV, herpes, psoriasis, atherosclerosis, alopecia, and autoimmune diseases such as rheumatoid arthritis .
Another method relates to inhibiting GSK-3, Aurora, or CDK-2 activity in a biological sample, which method comprises contacting the biological sample with the GSK-3 or Aurora inhibitor of formula V, or a pharmaceutical composition thereof, in an amount effective to inhibit GSK-3, Aurora or CDK-2.
Each of the aforementioned methods directed to the inhibition of GSK-3, Aurora or CDK-2, or the treatment of a disease alleviated thereby, is preferably carried out with a preferred compound of formula V, as described above .
Another embodiment of this invention relates to compounds of formula VI :
VI or a pharmaceutically acceptable derivative or prodrug thereof, wherein: G is Ring C or Ring D;
Ring C is selected from a phenyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, or 1, 2, 4-triazinyl ring, wherein said Ring C has one or two ortho substituents independently selected from -R1, any substitutable non- ortho carbon position on Ring C is independently substituted by -R5, and two adjacent substituents on Ring C are optionally taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-6 membered ring having 0-3 heteroatoms selected from oxygen, sulfur or nitrogen, said fused ring being optionally substituted by halo, oxo, or -R8; Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein Ring D is substituted at any substitutable ring carbon by oxo or -R5, and at any substitutable ring nitrogen by -R4, provided that when Ring D is a six-membered aryl or heteroaryl ring, -R5 is hydrogen at each ortho carbon position of Ring D; R1 is selected from -halo, -CN, -N02, T-V-R6, phenyl, 5-6 membered heteroaryl ring, 5-6 membered heterocyclyl ring, or Cι-6 aliphatic group, said phenyl, heteroaryl, and heterocyclyl rings each optionally substituted by up to three groups independently selected from halo, oxo, or -R8, said Cι_6 aliphatic group optionally substituted with halo, cyano, nitro, or oxygen, or R1 and an adjacent substituent taken together with their intervening atoms form said ring fused to Ring C;
Rγ is T-R3' ;
T is a valence bond or a d_ alkylidene chain;
R2 and R2' are independently selected from -R, -T-W-R6, or R2 and R2' are taken together with their intervening atoms to form a fused, 5-8 membered, unsaturated or partially unsaturated, ring having 0-3 ring heteroatoms selected from nitrogen, oxygen, or sulfur, wherein each substitutable carbon on said fused ring formed by R2 and R2' is substituted by halo, oxo, -CN, -N02, -R7, or -V-R6, and any substitutable nitrogen on said ring formed by R2 and R2' is substituted by R4;
R3' is an optionally substituted group selected from Cι-6 aliphatic, C3-ι0 carbocyclyl, C6-ιo aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms; each R is independently selected from hydrogen or an optionally substituted group selected from Cι-6 aliphatic, C3-10 aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms ; each R4 is independently selected from -R7, -COR7,
-C02 (optionally substituted d-6 aliphatic) , -C0N(R7)2, or -S02R7, or two R4 on the same nitrogen are taken together to form a 5-8 membered heterocyclyl or heteroaryl ring; each R5 is independently selected from -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -C0N(R4)2, -S02N(R)2, -OC(=0)R, -N(R4)C0R, -N(R4) C02 (optionally substituted Cι-6 aliphatic) , -N(R4)N(R4)2, -C=NN(R4)2, -C=N-OR, -N (R4) CON (R4) 2, -N(R)S02N(R4)2, -N(R4)S02R, or -OC (=0)N(R4) 2, or R5 and an adjacent substituent taken together with their intervening atoms form said ring fused to Ring C; V is -0-, -S-, -SO-, -SO2-, -N(R6)S02-, -S02N(R6)-, -N(R6)-, -CO-, -CO2-, -N(R6)CO-, -N(R6)C(0)0-, -N(R6)CON(R6) -, -N(R6)S02N(R5) -, -N (R6) N (R6) - ,
-C(0)N(R6)-, -OC(0)N(R6)-, -C(R6)20-, -C(R6)2S-, -C(R6)2SO-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C (R6) 2N (R6) - , -C(R6)2N(R6)C(0)-, -C(R6)2N(R6)C(0)0-, -C (R6) =NN(R6) - , -C(Rs)=N-0-, -C(R6)2N(R6)N(R6) -, -C (R6) 2N(R6) S02N(R6) - , or -C(R6)2N(R6)CON(R6) -;
W is -C(R6)20-, -C(R6)2S-, -C(R6)2SO-, -C(Rε)2S02-, -C(R6)2S02N(R6)-, -C(Rε)2N(R6)-, -CO-, -C02-, -C(R6)OC(0)-, -C(Rε)OC(0)N(R6) -, -C (R6) 2N(R6) CO- , -C(R6)2N(R6)C(0)0-, -C(R6)=NN(R6) -, -C(R6)=N-0-, -C(R6)2N(R6)N(R6) -, -C (R6) 2N(R?) S02N (R6) - , -C(R6)2N(R6)CON(R6) -, or -CON(R6)-; each R6 is independently selected from hydrogen, an optionally substituted d-4 aliphatic group, or two R6 groups on the same nitrogen atom are taken together with the nitrogen atom to form a 5-6 membered heterocyclyl or heteroaryl ring; each R7 is independently selected from hydrogen or an optionally substituted Cι_s aliphatic group, or two R7 on the same nitrogen are taken together with the nitrogen to form a 5-8 membered heterocyclyl or heteroaryl ring; and each R8 is independently selected from an optionally substituted -4 aliphatic group, -OR6, -SR6, -COR6, -S02R6, -N(R6)2, -N(R6)N(R6)2, -CN, -N02, -CON(R6)2, or -C02R6.
Preferred Rγ groups of formula VI include T-R3' wherein T is a valence bond or a methylene, and R3' is an optionally substituted group selected from d-6 aliphatic, C3-10 carbocyclyl, C6-10 aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms. A preferred R3' group is an optionally substituted group selected from C3-6 carbocyclyl, phenyl, or a 5-6 membered heteroaryl or heterocyclyl ring. Examples of preferred Ry include 2-pyridyl, 4-pyridyl, piperidinyl, morpholinyl, cyclopropyl, cyclohexyl, and optionally substituted phenyl such as phenyl or halo-substituted phenyl .
The R2 and R2' groups of formula VI may be taken together to form a fused ring, thus providing a bicyclic ring system containing a pyrazole ring. Preferred fused rings include benzo, pyrido, pyrimido, and a partially unsaturated 6-membered carbocyclo ring. These are exemplified in the following formula VI compounds having a pyrazole-containing bicyclic ring system:
Preferred substituents on the R2/R2' fused ring include one or more of the following: -halo, -N(R4)2, -C1-4 alkyl, -Cι-4 haloalkyl, -N02, -O (Cι-4 alkyl) , -C02(Cχ- alkyl), -CN, -S02 (d-4 alkyl) , -S02NH2, -OC(0)NH2, -NH2S02(Cι-4 alkyl) , -NHC (O) (C1-4 alkyl) , -C(0)NH2, and -CO (Cι._4 alkyl) , wherein the (d_4 alkyl) is a straight, branched, or cyclic alkyl group. Preferably, the (Cχ-4 alkyl) group is methyl. When the pyrazole ring system is monocyclic, preferred R2 groups of formula VI include hydrogen, C1-4 aliphatic, alkoxycarbonyl, (un) substituted phenyl, hydroxyalkyl, alkoxyalkyl, aminocarbonyl, mono- or dialkylaminocarbonyl, aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl , phenylaminocarbonyl , and (N- heterocyclyl) carbonyl. Examples of such preferred R2 substituents include methyl, cyclopropyl, ethyl, isopropyl, propyl, t-butyl, cyclopentyl, phenyl, C02H, Cθ2CH3, CH20H, CH2OCH3, CH2CH2CH2OH, CH2CH2CH2OCH3 ,
CH2CH2CH2OCH2Ph, CH2CH2CH2NH2 , CH2CH2CH2NHCOOC (CH3) 3 , CONHCH(CH3)2, CONHCH2CH=CH2, CONHCH2CH2OCH3 , CONHCH2Ph, CONH (eyelohexyl) , CON(Et)2, CON(CH3) CH2Ph, CONH (n-C3H7) , CON(Et)CH2CH2CH3, CONHCH2CH (CH3) 2n CON (n-C3H7) 2, CO(3- methoxymethylpyrrolidin-1-yl) , CONH(3-tolyl) , CONH(4- tolyl) , CONHCH3, CO(morpholin-l-yl) , CO (4-methylpiperazin- 1-yl), CONHCH2CH2OH, CONH2, and CO (piperidin-1-yl) . A preferred R2' group is hydrogen.
When G is Ring C, preferred formula VI Ring C groups are phenyl and pyridinyl. When two adjacent substituents on Ring C are taken together to form a fused ring, Ring C is contained in a bicyclic ring system. Preferred fused rings include a benzo or pyrido ring. Such rings preferably are fused at ortho and meta positions of Ring C. Examples of preferred bicyclic Ring C systems include naphthyl and isoquinolinyl. Preferred R1 groups include -halo, an optionally substituted Cι-6 aliphatic group, phenyl, -COR6, -OR6, -CN, -S02R6, -S02NH2, -N(R6)2, -C02R6, -CONH2, -NHCOR6, -0C(0)NH2, or -NHS02R6. When R1 is an optionally substituted d-6 aliphatic group, the most preferred optional substituents are halogen. Examples of preferred R1 groups include -CF3, -Cl, -F,' -CN, -C0CH3, -0CH3, -OH, -CH2CH3, -0CH2CH3, -CH3, -CF2CH3, cyclohexyl, t-butyl, isopropyl, cyclopropyl, -C≡CH, -C≡C-CH3, -S02CH3, -S02NH2, -N(CH3)2, -C02CH3, -CONH2, -NHCOCHs, -OC(0)NH2, -NHS02CH3, and -0CF3.
On Ring C preferred R5 substituents, when present, include -halo, -CN, -N02, -N(R)2, optionally substituted Cι-6 aliphatic group, -OR, -C(0)R, -C0R, -CONH(R4), -N(R)C0R, -S02N(R4)2, and -N (R4) S02R. More preferred R5 substituents include -Cl, -F, -CN, -CF3, -NH2, -NH(d_4 aliphatic), -N(d-4 aliphatic)2, -0(d-4 aliphatic), d- aliphatic, and -C02(Cι-4 aliphatic).
Examples of such preferred R5 substituents include -Cl, -F, -CN, -CF3, -NH2, -NHMe, -NMe2, -OEt, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, and -C02Et.
When G is Ring D, preferred formula VI Ring D monocyclic rings include substituted and unsubstituted phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, thienyl, azepanyl, and morpholinyl rings. When two adjacent substituents on Ring D are taken together to form a fused ring, the Ring D system is bicyclic. Preferred formula VI Ring D bicyclic rings include 1, 2 , 3 , 4-tetrahydroisoquinolinyl, 1,2,3,4- tetrahydroquinolinyl, 2 , 3-dihydro-lH-isoindolyl , 2,3- dihydro-lH-indolyl, isoquinolinyl, quinolinyl, and naphthyl . Examples of more pre erred bicyclic Ring D systems include naphthyl and isoquinolinyl.
Preferred substituents on formula VI Ring D include one or more of the following: halo, oxo, CN, -N02, -N(R)2, -C02R, -C0NH(R4), -N(R4)COR, -S02N(R4)2, -N(R4)S02R, -SR, -OR, -C(0)R, or substituted or unsubstituted group selected from 5-6 membered heterocyclyl, C6-ι0 aryl, or Cι-ε aliphatic . More preferred Ring D substituents include -halo, -CN, -oxo, -SR, -OR, -N(R)2, -C(0)R, or a substituted or unsubstituted group selected from 5-6 membered heterocyclyl, C6-ιo aryl, or Cι-6 aliphatic. Examples of Ring D substituents include -OH, phenyl, methyl, CH2OH, CH2CH2OH, pyrrolidinyl, OPh, CF3', C≡CH, Cl, Br, F, I, NH2, C(0)CH3, i-propyl, tert-butyl, SEt, OMe, N(Me)2, methylene dioxy, and ethylene dioxy.
Preferred formula VI compounds have one or more, and more preferably all, of the features selected from the group consisting of:
(a) Ring C is selected from a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is selected from a naphthyl, quinolinyl or isoquinolinyl ring, and R1 is -halo, an optionally substituted d-6 aliphatic group, phenyl, -COR6, -OR6, -CN, -S02R6, -S02NH2, -N(R6)2, -C02R6, -CONH2, -NHCOR6, -OC(0)NH2, or -NHS02R6; or Ring D is an optionally substituted ring selected from a phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, thienyl, azepanyl, morpholinyl, 1,2,3,4- tetrahydroisoquinolinyl, 1, 2, 3 , 4-tetrahydroquinolinyl, 2 , 3 -dihydro- 1H-isoindolyl , 2 , 3 -dihydro- 1H-indolyl, isoquinolinyl, quinolinyl, or naphthyl ring;
(b) Ry is T-R3', wherein T is a valence bond or a methylene; and (c) R2' is hydrogen and R2 is hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a Cα-6 aliphatic group, or R2 and R2' are taken together with their intervening atoms to form a substituted or unsubstituted benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring.
More preferred compounds of formula VI have one or more, and more preferably all, of the features selected from the group consisting of : (a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is a naphthyl ring, and R1 is -halo, a Ci-6 haloaliphatic group, a d_6 aliphatic group, phenyl, or -CN; or Ring D is an optionally substituted ring selected from phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, morpholinyl, 1,2,3, 4 -tetrahydroisoquinolinyl, 1,2,3,4- tetrahydroqumolmyl, 2, 3-dihydro-lH-isoindolyl, 2,3- dihydro-lH- indolyl, isoquinolinyl, quinolinyl, or naphthyl ,-
(b) Rγ is T-R3', wherein T is a valence bond or a methylene and R3' is an optionally substituted group selected from Ci-6 aliphatic, C3.6 carbocyclyl, C6-ι0 aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms;
(c) R2' is hydrogen and R2 is hydrogen or a substituted or unsubstituted group selected from aryl, or a d-6 aliphatic group, or R2 and R2' are taken together with their intervening atoms to form a substituted or unsubstituted benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring; and
(d) Ring D is substituted by oxo or R5, wherein each R5 is independently selected from -halo, -CN, -N02,
-N(R )2, optionally substituted Cι_6 aliphatic group, -OR, -C(0)R, -C02R, -CONH(R4), -N(R4)COR, -S02N(R4)2, or -N(R )S02R.
Even more preferred compounds of formula VI have one or more, and more preferably all, of the features selected from the group consisting of:
(a) Rγ is T-R3', wherein T is a valence bond or a methylene and R3' is an optionally substituted group selected from C1-4 aliphatic, C3-ε carbocyclyl, phenyl, or a 5-6 membered heteroaryl or heterocyclyl ring;
(b) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is a naphthyl ring, and R1 is -halo, a Cι-4 aliphatic group optionally substituted with halogen, or -CN; or Ring D is an optionally substituted ring selected from phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, morpholinyl, 1,2,3, 4-tetrahydroisoquinolinyl, 1,2,3,4- tetrahydroquinolinyl, isoquinolinyl, quinolinyl, or naphthyl ,-
(c) R2 and R2' are taken together with their intervening atoms to form a benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring optionally substituted with -halo, -N(R4)2, -d-4 alkyl, -Ci-4 haloalkyl, -N02, -O (Cι-4 alkyl) , -C02 (d-4 alkyl) , -CN, -S02 (d-4 alkyl) , -S02NH2, -OC(0)NH2, -NH2S02 (d-4 alkyl) , -NHC(O) (Ci-4 alkyl) , -C(0)NH2, or -CO (d-4 alkyl) , wherein the (d-4 alkyl) is a straight, branched, or cyclic alkyl group ,- and
(d) Ring D is substituted by oxo or R5, wherein each R5 is independently selected from -Cl, -F, -CN, -CF3, -NH2, -NH(d_4 aliphatic), -N(d-4 aliphatic)2, -0(Cι-4 aliphatic), Cι_4 aliphatic, and -C02(Cι-4 aliphatic)'.
Another embodiment of this invention relates to compounds of formula Via:
Via
or a pharmaceutically acceptable derivative or prodrug thereof , wherein: G is Ring C or Ring D;
Ring C is selected from a phenyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, or 1, 2, -triazinyl ring, wherein said Ring C has one or two ortho substituents independently selected from -R1, any substitutable non- ortho carbon position on Ring C is independently substituted by -R5, and two adjacent substituents on Ring C are optionally taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-6 membered ring having 0-3 heteroatoms selected from oxygen, sulfur or nitrogen, said fused ring being optionally substituted by halo, oxo, or -Rs;
Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein Ring D is substituted at any substitutable ring carbon by oxo or -R5, and at any substitutable ring nitrogen by -R4, provided that when Ring D is a six-membered aryl or heteroaryl ring, -R5 is hydrogen at each ortho carbon position of Ring D; R1 is selected from -halo, -CN, -N02, T-V-R6, phenyl, 5-6 membered heteroaryl ring, 5-6 membered heterocyclyl ring, or Cχ-6 aliphatic group, said phenyl, heteroaryl, and heterocyclyl rings each optionally substituted by up to three groups independently selected from halo, oxo, or -R8, said Cχ-6 aliphatic group optionally substituted with halo, cyano, nitro, or oxygen, or R1 and an adjacent substituent taken together with their intervening atoms form said ring fused to Ring C; T is a valence bond or a Cι_4 alkylidene chain; R2 and R2' are taken together with their intervening atoms to form a fused, 5-8 membered, unsaturated or partially unsaturated, ring having 0-3 ring heteroatoms selected from nitrogen, oxygen, or sulfur, wherein each substitutable carbon on said fused ring formed by R2 and R2' is substituted by halo, oxo, -CN, -N02, -R7, or -V-R6, and any substitutable nitrogen on said ring formed by R2 and R2' is substituted by R4; each R is independently selected from hydrogen or an optionally substituted group selected from d-s aliphatic, C6.10 aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms ; each R4 is independently selected from -R7, -COR7,
-C02 (optionally substituted Cι-S aliphatic) , -CON(R7)2, or -S02R7, or two R4 on the same nitrogen are taken together to form a 5-8 membered heterocyclyl or heteroaryl ring; each R5 is independently selected from -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -CON(R4)2, -S02N(R4)2, ~0C(=0)R, -N(R4)COR, -N(R4) C02 (optionally substituted Cι-6 aliphatic) , -N(R4)N(R4)2/ -C=NN(R4)2, -C=N-OR, -N (R4) CON (R4) 2, -N(R4)S02N(R)2, -N(R4)S02R, or -OC (=0) N(R4) 2, or R5 and an adjacent substituent taken together with their intervening atoms form said ring fused to Ring C;
V is -0-, -S-, -SO-, -S02-, -N(R6)S02-, -S02N(R6)-, -N(R6)-, -CO-, -C02-, -N(R6)C0-, -N(R6) C (O) O- , -N(R6)CON(R6) -, -N(Rs)S02N(R6) -, -N (Re) N (R6) - , -C(0)N(R6)-, -OC(0)N(R6) -,' -C(R6)20-, -C(Re)2S-, -C(R6)2SO-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C (R6) 2N (R6) - , -C(R6)2N(R6)C(0)-, -C(R6)2N(R6)C(0)0-, -C (R6) =NN (R6) - , -C(R6)=N-0-, -C(R6)2N(R6)N(R6) -, -C (Rs) 2N (R6) S02N (R6) - , or -C(R6)2N(R6)C0N(R6) -;
W is -C(R6)20-, -C(R6)2S-, -C(R6)2SO-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C(R6)2N(R6)-, -CO-, -C02-, -C(R6)OC(0) -, -C(R6)OC(0)N(R6) -, -C (R6) 2N (R6) CO- , -C(R6)2N(R6)C(0)0-, -C(R6)=NN(R6) -, -C(R6)=N-0-, -C(R6)2N(R6)N(R6) -, -C(R6)2N(Rε)S02N(R6) -, -C(R6)2N(R6)CON(R6) - , or -CON(R6)-; each R6 is independently selected from hydrogen, an optionally substituted C1-4 aliphatic group, or two R6 groups on the same nitrogen atom are taken together with the nitrogen atom to form a 5-6 membered heterocyclyl or heteroaryl ring; each R7 is independently selected from hydrogen or an optionally substituted Cι-6 aliphatic group, or two R7 on the same nitrogen are taken together with the nitrogen to form a 5-8 membered heterocyclyl or heteroaryl ring; and each R8 is independently selected from an optionally substituted d-4 aliphatic group, -OR6, -SR6, -COR6, -S02R6, -N(R6)2, -N(R6)N(R6)2, -CN, -N02, -CON(R6)2, or
-C02Rε.
Preferred rings formed by the R2 and R2' groups of formula Via include benzo, pyrido, pyrimido, and a partially unsaturated 6-membered carbocyclo ring. These are exemplified in the following formula Via compounds having a pyrazole-containing bicyclic ring system:
Preferred substituents on the R2/R2' fused ring include one or more of the following: -halo, -N(R4)2, -C1-4 alkyl, -d-4 haloalkyl, -N02, -O (Cι-4 alkyl) , -C02(Cι-4 alkyl), -CN, -S02 (d-4 alkyl) , -S02NH2, -OC(0)NH2,
-NH2S02(Cι_4 alkyl) , -NHC(O) (Cι-4 alkyl) , -C(0)NH2, and -CO (Cι-4 alkyl) , wherein the (Cι-4 alkyl) is a straight, branched, or cyclic alkyl group. Preferably, the (Cι- alkyl) group is methyl. When G is Ring C, preferred formula Via Ring C groups are phenyl and pyridinyl . When two adj acent substituents on Ring C are taken together to form a fused ring, Ring C is contained in a bicyclic ring system. Preferred fused rings include a benzo or pyrido ring. Such rings preferably are fused at ortho and meta positions of Ring C. Examples of preferred bicyclic Ring C systems include naphthyl and isoquinolinyl. Preferred R1 groups include -halo, an optionally substituted Ci-6 aliphatic group, phenyl, -COR6, -OR6, -CN, -S02R6, -S02NH2, -N(R6)2, -C02R6, -CONH2, -NHCOR5, -0C(0)NH2, or -NHS02Rδ .
When R1 is an optionally substituted Cι-6 aliphatic group, the most preferred optional substituents are halogen. Examples of preferred R1 groups include -CF3, -Cl, -F, -CN, -COCH3, -OCH3, -OH, -CH2CH3, -0CH2CH3, -CH3, -CF2CH3, cyclohexyl, t-butyl, isopropyl, cyclopropyl, -C≡CH, -C≡C-CH3, -S02CH3, -S02NH2, -N(CH3)2, -C02CH3, -CONH2, -NHCOCH3, -OC(0)NH2, -NHS02CH3, and -OCF3. On Ring C preferred R5 substituents, when present, include -halo, -CN, -N02, -N(R4) , optionally substituted Cι-6 aliphatic group, -OR, -C(0)R, -C02R, -C0NH(R4), -N(R4)COR, -S02N(R4)2, and -N (R4) S02R. More preferred R5 substituents include -Cl, -F, -CN, -CF3, -NH2, -NH(Ci-4 aliphatic), -N(Cι_4 aliphatic)2, -0(Cι-4 aliphatic), Cι- aliphatic, and -C02(Cχ-4 aliphatic). Examples of such preferred R5 substituents include -Cl, -F, -CN, -CF3, -NH2, -NHMe, -NMe2, -OEt, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, and -C02Et. When G is Ring D, preferred formula Via Ring D monocyclic rings include substituted and unsubstituted phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, thienyl, azepanyl, and morpholinyl rings. When two adjacent substituents on Ring D are taken together to form a fused ring, the Ring D system is bicyclic. Preferred formula Via Ring D bicyclic rings include 1, 2, 3, -tetrahydroisoquinolinyl, 1,2,3,4- tetrahydroquinolinyl , 2 , 3-dihydro-1H-isoindolyl , 2,3- dihydro-liϊ-indolyl, isoquinolinyl, quinolinyl, and naphthyl. Examples of more preferred bicyclic Ring D systems include naphthyl and isoquinolinyl.
Preferred substituents on the formula Via Ring D include one or more of the following: halo, oxo, CN, -N02, -N(R4)2, -C02R, -CONH(R4), -N(R4)COR, -S02N(R4)2, -N(R4)S02R, -SR, -OR, -C(0)R, or substituted or unsubstituted group selected from 5-6 membered heterocyclyl, C6-ιo aryl, or d-6 aliphatic. More preferred Ring D substituents include -halo, -CN, -oxo, -SR, -OR, -N(R)2, -C(0)R, or a substituted or unsubstituted group selected from 5-6 membered heterocyclyl, C6-ιo aryl, or Cι_6 aliphatic. Examples of Ring D substituents include -OH, phenyl, methyl, CH2OH, CH2CH2OH, pyrrolidinyl, OPh, CF3, CsCH, Cl, Br, F, I, NH2, C(O) CH3, i-propyl, tert-butyl, SEt, OMe, N(Me)2, methylene dioxy, and ethylene dioxy. Preferred formula Via compounds have one or more, and more preferably all, of the features selected from the group consisting of: (a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is selected from a naphthyl, quinolinyl or isoquinolinyl ring, and R1 is -halo, an optionally substituted Cι_6 aliphatic group, phenyl, -COR6, -OR6, -CN, -S02R6, -S02NH2, -N(R6)2, -C02R6, -CONH2, -NHCOR6, -OC(0)NH2, or -NHS02R6; or Ring D is an optionally substituted ring selected from a phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, thienyl , azepanyl , morpholinyl , 1,2,3,4- tetrahydroisoquinolinyl, 1,2,3,4-tetrahydroquinolinyl , 2, 3-dihydro-lH-isoindolyl, 2, 3-dihydro-1H-indolyl, isoquinolinyl, quinolinyl, or naphthyl ring; and
(b) R2 and R2' are taken together with their intervening atoms to form a substituted or unsubstituted benzo, pyrido, pyrimido or partially unsaturated 6- membered carbocyclo ring.
More preferred compounds of formula V a have one or more, and more preferably all, of the features selected from the group consisting of:
(a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is a naphthyl ring, and R1 is -halo, a d-6 haloaliphatic group, a d-6 aliphatic group, phenyl, or -CN; or Ring D is an optionally substituted ring selected from phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, morpholinyl, 1,2,3, 4-tetrahydroisoquinolinyl, 1,2,3,4- tetrahydroquiholinyl, 2, 3 -dihydro-lH-isoindolyl, 2,3- dihydro-lH-indolyl, isoquinolinyl, quinolinyl, or naphthyl ; (b) R2 and R2' are taken together with their intervening atoms to form a benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring optionally substituted with -halo, -N(R4)2, -Cι-4 alkyl, -Ci-4 haloalkyl, -N02, -O (Cι_4 alkyl) , -C02 (d-4 alkyl) , -CN, -S02(d-4 alkyl) , -S02NH2, -0C(0)NH2, -NH2S02 (d-4 alkyl) ,
-NHC(O) (d-4 alkyl) , -C(0)NH2, and -CO (d-4 alkyl) , wherein the (d-4 alkyl) is a straight, branched, or cyclic alkyl group; and
(c) Ring D is substituted by oxo or R5, wherein each R5 is independently selected from -halo, -CN, -N02, -N(R4)2, optionally substituted Cι-6 aliphatic group, -OR, -C(0)R, -C02R, -CONH(R4), -N(R4)COR, -S02N(R4)2, or -N(R4)S02R.
Even more preferred compounds of formula Via have one or more, and more preferably all, of the features selected from the group consisting of :
(a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is a naphthyl ring, and R1 is -halo, a Cι- aliphatic group optionally substituted with halogen, or -CN; or Ring D is an optionally substituted ring selected from phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, morpholinyl, 1,2,3, 4-tetrahydroisoquinolinyl, 1,2,3,4- tetrahydroquinolinyl, isoquinolinyl, quinolinyl, or naphthyl ; (b) R2 and R2' are taken together with their intervening atoms to form a benzo, pyrido, or partially unsaturated 6-membered carbocyclo ring optionally substituted with -halo, -N(R4)2, -d_4 alkyl, -Cχ- haloalkyl, -N02, -0 (Cι-4 alkyl) , -C02 (d-4 alkyl) , -CN, -S02(d-4 alkyl) , -S02NH2, -OC(0)NH2, -NH2S02 (d-4 alkyl) ,
-NHC(O) ( - alkyl) , -C(0)NH2, or -CO (d-4 alkyl) , wherein the (Cι- alkyl) is a straight, branched, or cyclic alkyl group ; and
(d) Ring D is substituted by oxo or R5, wherein each R5 is independently selected from -Cl, -F, -CN, -CF3, -NH2, -NH(d-4 aliphatic), -N(Cι- aliphatic)2, -0(d-4 aliphatic), d-4 aliphatic, and -C0 (C1.4 aliphatic).
Representative compounds of formula VI and IVa are set forth in Table 5 below.
Table 5
VI - 1 VI-2 VI- 3
VI-7 VI-8 VI-9
VI-10 VI-11 VI -12
VI- 13 VI-14 VI-15 -16 VI-17
VI-19 VI-20 VI-21
VI-35 VI-36
VI-40 VI-41 VI-42
-45
In another embodiment, this invention provides a composition comprising a compound of formula VI or Via and a pharmaceutically acceptable carrier. One aspect of this invention relates to a method of inhibiting GSK-3 activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula VI or Via. Another aspect relates to a method of treating a disease that is alleviated by treatment with a GSK-3 inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula VI or Via.
Another aspect relates to a method of enhancing glycogen synthesis and/or lowering blood levels of glucose in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula VI or Via. This method is especially useful for diabetic patients . Another aspect relates to a method of inhibiting the production of hyperphosphorylated Tau protein in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula VI or Via. This method is especially useful in halting or slowing the progression of Alzheimer's disease.
Another aspect relates to a method of inhibiting the phosphorylation of β-catenin in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula VI or Via. This method is especially useful for treating schizophrenia.
One aspect of this invention relates to a method of inhibiting Aurora activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula VI or Via.
Another aspect relates to a method of treating a disease that is alleviated by treatment with an Aurora inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula VI or Via. This method is especially useful for treating cancer, such as colon, ovarian, and breast cancer.
One aspect of this invention relates to a method of inhibiting CDK-2 activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula VI or Via.
Another aspect relates to a method of treating a disease that is alleviated by treatment with a CDK-2 inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula VI or Via. This method is especially useful for treating cancer, Alzheimer's disease, restenosis, angiogenesis, glomerulonephritis, cytomegalovirus, HIV, herpes, psoriasis, atherosclerosis, alopecia, and autoimmune diseases such as rheumatoid arthritis.
Another method relates to inhibiting GSK-3, Aurora, or CDK-2 activity in a biological sample, which method comprises contacting the biological sample with the GSK-3 or Aurora inhibitor of formula VI or Via, or a pharmaceutical composition thereof,, in an amount effective to inhibit GSK-3, Aurora or CDK-2. Each of the aforementioned methods directed to the inhibition of GSK-3, Aurora or CDK-2, or the treatment of a disease alleviated thereby, is preferably carried out with a preferred compound of formula VI or Via, as described above. Another embodiment of this invention relates to compounds of formula VII:
VII
or a pharmaceutically acceptable derivative or prodrug thereof, wherein: G is Ring C or Ring D;
Ring C is selected from a phenyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, or 1, 2 , 4-triazinyl ring, wherein said Ring C has one or two ortho substituents independently selected from -R1, any substitutable non- ortho carbon position on Ring C is independently substituted by -R5, and two adjacent substituents on Ring C are optionally taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-6 membered ring having 0-3 heteroatoms selected from oxygen, sulfur or nitrogen, said fused ring being optionally substituted by halo, oxo, or -R8; Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein Ring D is substituted at any substitutable ring carbon by oxo or
-R5, and at any substitutable ring nitrogen by -R4, provided that when Ring D is a six-membered aryl or heteroaryl ring, -R5 is hydrogen at each ortho carbon position of Ring D; R1 is selected from -halo, -CN, -N02, T-V-R6, phenyl, 5-6 membered heteroaryl ring, 5-6 membered heterocyclyl ring, or Cι-6 aliphatic group, said phenyl, heteroaryl, and heterocyclyl rings each optionally substituted by up to three groups independently selected from halo, oxo, or -R8, said Cι-6 aliphatic group optionally substituted with halo, cyano, nitro, or oxygen, or R1 and an adjacent substituent taken together with their intervening atoms form said ring fused to Ring C;
Ry is hydrogen or T-R3";
T is a valence bond, hydrogen, or a d-4 alkylidene chain;
R2 and R2' are independently selected from -R, -T-W-R6, or R2 and R2' are taken together with their intervening atoms to form a fused, 5-8 membered, unsaturated or partially unsaturated, ring having 0-3 ring heteroatoms selected from nitrogen, oxygen, or sulfur, wherein each substitutable carbon on said fused ring formed by R2 and R2' is substituted by halo, oxo, -CN, -N02, -R7, or -V-R6, and any substitutable nitrogen on said ring formed by R2 and R2' is substituted by R4 ;
R3" is selected from an optionally substituted group selected from C3_ι0 carbocyclyl, C6-ιo aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms; each R is independently selected from hydrogen or an optionally substituted group selected from d-6 aliphatic, C6-ι0 aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms ; each R4 is independently selected from -R7, -COR7,
-C02 (optionally substituted d-6 aliphatic) , -CON(R7)2, or -S02R7, or two R4 on the same nitrogen are taken together to form a 5-8 membered heterocyclyl or heteroaryl ring; each R5 is independently selected from -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -CON(R)2, -S02N(R4)2, -0C(=0)R, -N(R4)C0R, -N(R4) C02 (optionally substituted Cι-S aliphatic) , -N(R4)N(R4)2, -C=NN(R4)2, -C=N-0R, -N (R4) CON (R4) 2, -N(R4)S02N(R4)2, -N(R4)S02R, or -OC (=0) N(R4) _ , or R5 and an adjacent substituent taken together with their intervening atoms form said ring fused to Ring C; V is -0-, -S-, -SO-, -S02-, -N(R6)S02-, -S02N(R6)-, -N(R6)-, -CO-, -CO2-, -N(R6)CO-, -N(R6) C (0) 0- , -N(R6)CON(R6) -, -N(R6)S02N(R6) -, -N (R6) N (R6) - , -C(0)N(R6)-, -0C(0)N(R6)-, -C(R6)20-, -C(R6)2S-, -C(R6)2SO-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C (R6) 2N (R6) - , -C(R6)2N(R6)C(0)-, -C(R6)2N(R6)C(0)0-, -C (R6) =NN (R6) - , -C(R6)=N-0-, -C(R6)2N(R6)N(R6)-, -C (R6) 2N (R5) S02N (R6) - , or -C(R6)2N(R6)CON(R6) -; W is -C(R6)20-, -C(R6)2S-, -C(R6)2SO-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C(RS)2N(R6)-, -CO-, -C02-, -C(R6)0C(0) -, -C(R6)0C(0)N(R6) -, -C (R6) 2N (R6) CO- , -C(R6)2N(R6)C(0)0-, -C(R6)=NN(R6)-, -C(R6)=N-0-, -C (R6) 2N (R6) N (R6) - , -C (R6) 2N (R6) S02N (R6) - , -C(R6)2N(R6)CON(R6) -, or -CON(R6)-; each R6 is independently selected from hydrogen, an optionally substituted d- aliphatic group, or two R6 groups on the same nitrogen atom are taken together with the nitrogen atom to form a 5-6 membered heterocyclyl or heteroaryl ring; each R7 is independently selected from hydrogen or an optionally substituted Cι-ε aliphatic group, or two R7 on the same nitrogen are taken together with the nitrogen to form a 5-8 membered heterocyclyl or heteroaryl ring; each R8 is independently selected from an optionally substituted Cι-4 aliphatic group, -OR6, -SR6, -COR6, -S02R6, -N(R6)2, -N(R6)N(R6)2, -CN, -N02, -CON(R6)2, or -C02R6; and R9 is selected from -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -CON(R4)2, -S02N(R4)2, -OC(=0)R, -N(R4)COR, -N (R4) C02 (optionally substituted Cχ.6 aliphatic) , -N(R4)N(R)2, -C=NN(R4)2, -C=N-OR, -N(R4)CON(R4)2, -N (R4) S02N (R4) 2, -N(R4)S02R, or -OC(=0)N(R4)2. Preferred Rγ groups of formula VII include T-R3" wherein T is a valence bond or a methylene. Preferred R3" groups include an optionally substituted group selected from C3_6 carbocyclyl, phenyl, or a 5-6 membered heteroaryl or heterocyclyl ring. Examples of preferred Rγ include 2-pyridyl, 4-pyridyl, piperidinyl, cyclopropyl, and an optionally substituted phenyl such as phenyl or halo-substituted phenyl.
The R2 and R2' groups of formula VII may be taken together to form a fused ring, thus providing a bicyclic ring system containing a pyrazole ring.
Preferred fused rings include benzo, pyrido, pyrimido, and a partially unsaturated 6-membered carbocyclo ring. These are exemplified in the following formula VII compounds having a pyrazole-containing bicyclic ring system:
Preferred substituents on the R2/R2' fused ring include one or more of the following: -halo, -N(R4)2, -Cι-4 alkyl, -Cι_4 haloalkyl, -N02, -O (d-4 alkyl) , -C02(C1.4 alkyl), -CN, -S02 (d_4 alkyl) , -S02NH2, -OC(0)NH2, -NH2S02(Cι-4 alkyl) , -NHC (O) (C1-4 alkyl) , -C(0)NH2, and -CO(Cχ-4 alkyl), wherein the (Cι_4 alkyl) is a straight, branched, or cyclic alkyl group. Preferably, the (Cι-4 alkyl) group is methyl.
When the pyrazole ring system of formula VII. is monocyclic, preferred R2 groups include hydrogen, d_4 aliphatic, alkoxycarbonyl, (un) substituted phenyl, hydroxyalkyl, alkoxyalkyl, aminocarbonyl, mono- or dialkylaminocarbonyl , aminoalkyl , alkylaminoalkyl , dialkylaminoalkyl, phenylaminocarbonyl, and (N- heterocyclyl) carbonyl . Examples of such preferred R2 substituents include methyl, cyclopropyl, ethyl, isopropyl, propyl, t-butyl, cyclopentyl, phenyl, C02H, C02CH3, CH2OH, CH2OCH3, CH2CH2CH2OH, CH2CH2CH2OCH3 , CH2CH2CH2OCH2Ph, CH2CH2CH2NH2, CH2CH2CH2NHCOOC (CH3) 3 , CONHCH(CH3)2, CONHCH2CH=CH2 , CONHCH2CH2OCH3 , CONHCH2Ph,
CONH (eyelohexyl) , CON(Et)2, CON(CH3) CH2Ph, CONH (n-C3H7) , CON(Et)CH2CH2CH3, CONHCH2CH (CH3) 2 , CON(n-C3H7) _ , CO(3- methoxymethylpyrrolidin-1-yl) , CONH (3 -tolyl) , CONH (4- tolyl) , CONHCH3, CO (morpholin-1-yl) , CO (4-methylpiperazin- 1-yl) , CONHCH2CH2OH, CONH2, and CO (piperidin-1-yl) . A preferred R2' group is hydrogen.
When G is Ring C, preferred formula VII Ring C groups are phenyl and pyridinyl. When two adjacent substituents on Ring C are taken together to form a fused ring, Ring C is contained in a bicyclic ring system. Preferred fused rings include a benzo or pyrido ring. Such rings preferably are fused at ortho and meta positions of Ring C. Examples of preferred bicyclic Ring C systems include naphthyl and isoquinolinyl. Preferred R1 groups include -halo, an optionally substituted Cι-6 aliphatic group, phenyl, -COR6, -OR6, -CN, -S02R6, -S02NH2, -N(R6)2, -C02R6, -C0NH2, -NHCOR6, -OC(0)NH2, or -NHS02R6. When R1 is an optionally substituted d-6 aliphatic group, the most preferred optional substituents are halogen. Examples of preferred R1 groups include -CF3, -Cl, -F, -CN, -COCH3, -0CH3, -OH, -CH2CH3, -0CH2CH3, -CH3, -CF2CH3, cyclohexyl, t-butyl, isopropyl, cyclopropyl, -C≡CH, -C≡C-CH3, -S02CH3, -S02NH2, -N(CH3)2, -C02CH3, -CONH2, -NHCOCH3, -OC(0)NH2, -NHS02CH3, and -OCF3 '.
On Ring C preferred R5 substituents, when present, include -halo, -CN, -N02, -N(R4)2, optionally substituted Cι_6 aliphatic group, -OR, -C(0)R, -C02R, -C0NH(R4), -N(R4)C0R, -S02N(R4)2, and -N(R4)S02R. More preferred R5 substituents include -Cl, -F, -CN, -CF3, -NH2, -NH(Cι-4 aliphatic), -N(d_4 aliphatic)2, -0(d-4 aliphatic), Cι-4 aliphatic, and -C02(Cι-4 aliphatic). Examples of such preferred R5 substituents include -Cl, -F, -CN, -CF3, -NH2, -NHMe, -NMe2, -OEt, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, and -C02Et.
When G is Ring D, preferred formula VII Ring D monocyclic rings include substituted and unsubstituted phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, thienyl, azepanyl, and morpholinyl rings. When two adjacent substituents on Ring D are taken together to form a fused ring, the Ring D system is bicyclic. Preferred formula VII Ring D bicyclic rings include 1, 2, 3 , 4-tetrahydroisoquinolinyl, 1,2,3,4- tetrahydroqumolinyl, 2 , 3-dihydro-lH-isoindolyl, .2,3- dihydro-lH-indolyl, isoquinolinyl, quinolinyl, and naphthyl . Examples of more preferred bicyclic Ring D systems include naphthyl and isoquinolinyl .
Preferred substituents on Ring D include one or more of the following: halo, oxo, CN, -N02, -N(R)2, -C02R, -CONH(R4), -N(R4)COR, -S02N(R4)2, -N(R)S02R, -SR, -OR, -C(0)R, or substituted or unsubstituted group selected from 5-6 membered heterocyclyl, C6-ιo aryl, or d-e aliphatic. More preferred Ring D substituents include -halo, -CN, -oxo, -SR, -OR, -N(R)2, -C(0)R, or a substituted or unsubstituted group selected from 5-6 membered heterocyclyl, Cg-io aryl, or C_.6 aliphatic. Examples of Ring D substituents include -OH, phenyl, methyl, CH2OH, CH2CH2OH, pyrrolidinyl, OPh, CF3, C≡CH, Cl, Br, F, I, NH2, C(0)CH3, i-propyl, tert-butyl, SEt, OMe, N(Me)2, methylene dioxy, and ethylene dioxy.
Preferred formula VII compounds have one or more, and more preferably all, of the features selected from the group consisting of :
(a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is selected from a naphthyl, quinolinyl or isoquinolinyl ring, and R1 is -halo, an optionally substituted Cι_6 aliphatic group, phenyl, -COR6, -OR6, -CN, -S02R6, -S02NH2, -N(R6)2, -C02R6, -CONH2, -NHCOR6, -OC(0)NH2, or -NHS02R6; or Ring D is an optionally substituted ring selected from a phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, thienyl, azepanyl, morpholinyl, 1,2,3,4- tetrahydroisoquinolinyl , 1,2,3,4-tetrahydroqumolinyl , 2 , 3 -dihydro-IH-isoindolyl , 2 , 3 -dihydro- 1H-indolyl , isoquinolinyl, quinolinyl, or naphthyl ring;
(b) Rγ is T-R3", wherein T is a valence bond or a methylene; and
(c) R2' is hydrogen and R2 is hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a Cχ-6 aliphatic group, or R2 and R2' are taken together with their intervening atoms to form a substituted or unsubstituted benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring. More preferred compounds of formula VII have one or more, and more preferably all, of the features selected from the group consisting of :
(a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is a naphthyl ring, and R1 is -halo, a Ci-6 haloaliphatic group, a Cι_6 aliphatic group, phenyl, or -CN; or Ring D is an optionally substituted ring selected from phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, morpholinyl, 1,2, 3, 4 -tetrahydroisoquinolinyl, 1,2,3,4- tetrahydroquinolinyl, 2 , 3 -dihydro-Iff-isoindolyl, 2,3- dihydro-Iff-indolyl, isoquinolinyl, quinolinyl, or naphthyl;
(b) Rγ is T-R3", wherein T is a valence bond or a methylene and R3" is an optionally substituted group selected from C3-e carbocyclyl, phenyl, or a 5-6 membered heteroaryl or heterocyclyl ring; (c) R2' is hydrogen and R2 is hydrogen or a substituted or unsubstituted group selected from aryl, or a d_6 aliphatic group, or R2 and R2' are taken together with their intervening atoms to form a substituted or unsubstituted benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring; and
(d) Ring D is substituted by oxo or R5, wherein each R5 is independently selected from -halo, -CN, -N02, -N(R4)2, optionally substituted d-6 aliphatic group, -OR, -C(0)R, -C02R, -CONH(R4), -N(R4)C0R, -S02N(R )2, or -N(R4)S02R.
Even more preferred compounds of formula VII have one or more, and more preferably all, of the features selected from the group consisting of : (a) Rγ is T-R3", wherein T is a valence bond or a methylene and R3" is an optionally substituted group selected from phenyl, or a 5-6 membered heteroaryl or heterocyclyl ring; (b) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is a naphthyl ring, and R1 is -halo, a Cι-4 aliphatic group optionally substituted with halogen, or -CN; or Ring D is an optionally substituted ring selected from phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, morpholinyl, 1,2, 3, 4-tetrahydroisoquinolinyl, 1,2,3,4- tetrahydroquinolinyl, isoquinolinyl, quinolinyl, or naphthyl ;
(c) R2 and R2' are taken together with their intervening atoms to form a benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring optionally substituted with -halo, -N(R)2, -Cι-4 alkyl, -Ci-4 haloalkyl, -N02, -0 (Cι_4 alkyl) , -C02 (Cx-4 alkyl) , -CN, -S02(C!-4 alkyl) , -S02NH2, -OC(0)NH2, -NH2S02 (Cι_4 alkyl) , -NHC(O) (Ci-4 alkyl) , -C(0)NH2, or -CO (Cι-4 alkyl) , wherein the (Cι_4 alkyl) is a straight, branched, or cyclic alkyl group; and (d) Ring D is substituted by oxo or R5, wherein each R5 is independently selected from -Cl, -F, -CN, -CF3, -NH2, -NH(d-4 aliphatic), -N(Cι_4 aliphatic)2, -0(d-4 aliphatic), d_4 aliphatic, and -C02(Cι_4 aliphatic).
Representative compounds of formula VII are set forth in Table 6 below.
Table 6. -1 VII-3
VII-4 VII -5 VII-6
VII-7 VII -8 VII -9
VII-13 VII-14 VII-15
VII-16 VII-17 VII-18
VII-22 VII-23 VII-24
VII-25 VII-26 VII-27
VII-28 VII-29 VII-30
VII-31 VII-32 VII-33
VII-34 VII-35 VII-36
In another embodiment, this invention provides a composition comprising a compound .of formula VII and a pharmaceutically acceptable carrier. One aspect of this invention relates to a method of inhibiting GSK-3 activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula VII.
Another aspect relates to a method of treating a disease that is alleviated by treatment with a GSK-3 inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula VII .
Another aspect relates to a method of enhancing glycogen synthesis and/or lowering blood levels of glucose in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula VII. This method is especially useful for diabetic patients .
Another aspect relates to a method of inhibiting the production of hyperphosphorylated Tau protein in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula VII. This method is especially useful in halting or slowing the progression of Alzheimer's disease.
Another aspect relates to a method of inhibiting the phosphorylation of β-catenin in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula VII. This method is especially useful for treating schizophrenia.
One aspect of this invention relates to a method of inhibiting Aurora activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula VII .
Another aspect relates to a method of treating a disease that is alleviated by treatment with an Aurora inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula VII . This method is especially useful for treating cancer, such as colon, ovarian, and breast cancer.
One aspect of this invention relates to a method of inhibiting CDK-2 activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula VII.
Another aspect relates to a method of treating a disease that is alleviated by treatment with a CDK-2 inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula VII . This method is especially useful for treating cancer, Alzheimer's disease, restenosis, angiogenesis, glomerulonephritis, cytomegalovirus, HIV, herpes, psoriasis, atherosclerosis, alopecia, and autoimmune diseases such as rheumatoid arthritis.
Another method relates to inhibiting GSK-3, Aurora, or CDK-2 activity in a biological sample, which method comprises contacting the biological sample with the GSK-3 or Aurora inhibitor of formula VII, or a pharmaceutical composition thereof, in an amount effective to inhibit GSK-3, Aurora or CDK-2. Each of the aforementioned methods directed to the inhibition of GSK-3, Aurora or CDK-2, or the treatment of a disease alleviated thereby, is preferably carried out with a preferred compound of formula VII, as described above.
Another embodiment of this invention relates to compounds of formula VIII:
VIII
or a pharmaceutically acceptable derivative or prodrug thereof, wherein:
Z1 is N or CR9, Z2 is N or CH, and Z3 is N or CRX, provided that one of Z1 and Z3 is nitrogen;
G is Ring C or Ring D;
Ring C is selected from a phenyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, or 1, 2 , 4-triazinyl ring, wherein said Ring C has one or two ortho substituents independently selected from -R1, any substitutable non- ortho carbon position on Ring C is independently substituted by -R5, and two adjacent substituents on Ring C are optionally taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-6 membered ring having 0-3 heteroatoms selected from oxygen, sulfur or nitrogen, said fused ring being optionally substituted by halo, oxo, or -R8; Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein Ring D is
. substituted at any substitutable ring carbon by halo, oxo, or -R5, and at any substitutable ring nitrogen by -R4, provided that when Ring D is a six-membered aryl or heteroaryl ring, -R5 is hydrogen at each ortho carbon position of Ring D;
R1 is. selected from -halo, -CN, -N02, T-V-R6, phenyl, 5-6 membered heteroaryl ring, 5-6 membered heterocyclyl ring, or d-6 aliphatic group, said phenyl, heteroaryl, and heterocyclyl rings each optionally substituted by up to three groups independently selected from halo, oxo, or -R8, said d-e aliphatic group optionally substituted with halo, cyano, nitro, or oxygen, or R1 and an adjacent substituent taken together with their intervening atoms form said ring fused to Ring C;
Rx is T-R3;
T is a valence bond or a Cι-4 alkylidene chain; R2 and R2' are independently selected from -R, -T-W-R6, or R2 and R2' are taken together with their intervening atoms to form a fused, 5-8 membered, unsaturated or partially unsaturated, ring having 0-3 ring heteroatoms selected from nitrogen, oxygen, or sulfur, wherein each substitutable carbon on said fused ring formed by R2 and R2' is substituted by halo, oxo, -CN, -N02, -R7, or -V-R6, and any substitutable nitrogen on said ring formed by R2 and R2' is substituted by R4;
R3 is selected from -R, -halo, -OR, -C(=0)R, -C02R, -COCOR, -COCH2COR, -N02, -CN, -S(0)R, -S(0)2R, -SR, -N(R4)2, -CON(R7)2, -S02N(R)2, -OC(=0)R, -N(R)C0R, -N(R7) C02 (optionally substituted d-6 aliphatic) , -N(R4)N(R4)2, -C=NN(R4)2, -C=N-OR, -N (R7) CON (R7) 2, -N(R7)S02N(R7)2, -N(R4)S02R, or -OC (=0)N(R7) 2; each R is independently selected from hydrogen or an optionally substituted group selected from d-6 aliphatic, C6-ιo aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms ; each R4 is independently selected from -R7, -COR7,
-C02 (optionally substituted d-6 aliphatic) , -C0N(R7)2, or -S02R7, or two R4 on the same nitrogen are taken together to form a 5-8 membered heterocyclyl or heteroaryl ring; each R5 is independently selected from -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -C0N(R)2, -S02N(R4)2, -OC (=0)R, -N(R4)COR, -N(R4) C02 (optionally substituted Ci-6 aliphatic) , -N(R)N(R)2, -C=NN(R4)2, -C=N-0R, -N (R4) CON (R4) _ ,
-N(R4)S02N(R4)2. -N(R4)S02R, or -OC (=0)N(R4) _ , or R5 and an adjacent substituent taken together with their intervening atoms form said ring fused to Ring C;
V is -0-, -S-, -SO-, -S02-, -N(R6)S02-, -S02N(R6)-, -N(R6)-, -CO-, -CO2-, -N(R6)CO-, -N (R6) C (O) O- , -N(R6)CON(R6) -, ■ -N(R6)S02N(R6) -, -N(R6)N(R6) -, -C(0)N(R6)-, -OC(0)N(R6) -, -C(R6)20-, -C(R6)2S-, -C(R6)2SO-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C (R6) 2N (R6) - , -C(R6)2N(R6)C(0)-, -C(R6)2N(R6)C(0)0-, -C (R6) =NN(R6) - , -C(R6)=N-0-, -C(R6)2N(R6)N(R6)-, -C (R6) 2N (R6) S02N(R6) - , or -C(R6)2N(R6)CON(R6) -;
W is -C(R6)20-, -C(R6)2S-, -C(R6)2SO-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C(R6)2N(R6)-, -CO-, -C02-, -C(R6)OC(0)-, -C(R6)OC(0)N(R6)-, -C (R6) 2N(R6) CO- , -C(R6)2N(R6)C(0)θ-, -C (R6) =NN (R6) - , -C(Re)=N-0-, -C (R6) 2N (R6) N (R6) - , -C (R6) 2N (R6) S02N (R6) - ,
-C(R6)2N(R6)CON(R6) -, or -CON(R6)-; each R6 is independently selected from hydrogen, an optionally substituted Cι_4 aliphatic group, or two R6 groups on the same nitrogen atom are taken together with" the nitrogen atom to form a 5-6 membered heterocyclyl or heteroaryl ring; each R7 is independently selected from hydrogen or an optionally substituted d-6 aliphatic group, or two R7 on the same nitrogen are taken together with the nitrogen to form a 5-8 membered heterocyclyl or heteroaryl ring; each R8 is independently selected from an optionally substituted C1-4 aliphatic group, -OR6, -SR6, -COR6, -S02R6, -N(R6)2, -N(Rε)N(R6)2, -CN, -N02, -CON(R6)2, or
-C02R6; and R9 is selected from -R, halo, -OR, -C(=0)R, -C02R, -COCOR,
-N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -CON(R4)2,
-S02N(R4)2, -OC(=0)R, -N(R4)C0R, - (R4) C02 (optionally substituted d-6 aliphatic) , -N(R4)N(R4) 2, -C=NN(R4)2,
-C=N-0R, -N(R)CON(R4)2, -N(R4) S02N (R4) 2, -N(R)S02R, or
-0C(=0)N(R4)2.
Accordingly, the present invention relates to compounds of formula Villa, Vlllb, VIIIc and Vllld as shown below:
Villa VIIlb VIIIc Vllld
Preferred Rx groups of formula VIII include T-R3 wherein T is a valence bond or a methylene and R3 is CN, -R, or -OR. When R3 is -R, preferred R3 groups include an optionally substituted group selected from d-6 aliphatic, phenyl, or a 5-6 membered heteroaryl or heterocyclyl ring. When R3 is -OR, preferred R groups include an optionally substituted group C_.5 aliphatic group such as alkyl- or dialkylaminoalkyl and aminoalkyl . Examples of preferred Rx include acetamido, CN, piperidinyl, piperazinyl, phenyl, pyridinyl, imidazol-1-yl, imidazol- 2-yl, cyclohexyl, cyclopropyl, methyl, ethyl, isopropyl, t-butyl, NH2CH2CH2NH, and NH2CH2CH20. Preferred R9 groups of formula VIII, when present, include R, OR, and N(R4)2. Examples of preferred R9 include methyl, ethyl, NH2, NH2CH2CH2NH, N(CH3) 2CH2CH2NH, N(CH3)2CH2CH20, (piperidin-1-yl) CH2CH20, and NH2CH2CH20. The R2 and R2' groups of formula VIII may be taken together to form a fused ring, thus providing a bicyclic ring system containing a pyrazole ring. Preferred fused rings include benzo, pyrido, pyrimido, and a partially unsaturated 6-membered carbocyclo ring. These are exemplified in the following formula VIII compounds having a pyrazole-containing bicyclic ring system:
Preferred substituents on the formula VIII R2/R2' fused ring include one or more of the following: -halo, -N(R4)2, -d-4 alkyl, -d-4 haloalkyl, -N02, -0(d-4 alkyl), -C02 (d_4 alkyl) , -CN, -S02 (Cι-4 alkyl) , -S02NH2, -OC(0)NH2, -NH2S02(C1.4 alkyl) , -NHC(O) (d-4 alkyl) , -C(0)NH2, and -CO (d-4 alkyl) , wherein the (Cι-4 alkyl) is a straight, branched, or cyclic alkyl group. Preferably, the (Cχ-4 alkyl) group is methyl. When the pyrazole ring system of formula VIII is monocyclic, preferred R2 groups include hydrogen, Cι_4 aliphatic, alkoxycarbonyl, (un) substituted phenyl, hydroxyalkyl, alkoxyalkyl, aminocarbonyl, mono- or dialkylaminocarbonyl, aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl , phenylaminocarbonyl , and (N- heterocyclyl) carbonyl. Examples of such preferred R2 substituents include methyl, cyclopropyl, ethyl, isopropyl, propyl, t-butyl, cyclopentyl, phenyl, C02H, C02CH3, CH2OH, CH2OCH3, CH2CH2CH2OH, CH2CH2CH2OCH3, CH2CH2CH2OCH2Ph, CH2CH2CH2NH2, CH2CH2CH2NHCOOC (CH3) 3,
CONHCH(CH3)2, CONHCH2CH=CH2, CONHCH2CH2OCH3 , C0NHCH2Ph, CONH (eyelohexyl) , CON (Et) 2 , CON (CH3) CH2Ph, CONH (n-C3H7) , CON(Et)CH2CH2CH3, CONHCH2CH (CH3) 2, CON(n-C3H7) 2, CO(3- methoxymethylpyrrolidin-1-yl) , CONH (3 -tolyl) , CONH (4- tolyl), CONHCH3, CO (morpholin-1-yl) , CO (4-methylpiperazin- 1-yl) , CONHCH2CH2OH, CONH2, and CO (piperidin-1-yl) . A preferred R2' group is hydrogen.
When G is Ring C, preferred formula VIII Ring C groups are phenyl and pyridinyl. When two adjacent substituents on Ring C are taken together to form a fused ring, Ring C is contained in a bicyclic ring system. Preferred fused rings include a benzo or pyrido ring. Such rings preferably are fused at ortho and. meta positions of Ring C. Examples of preferred bicyclic Ring C systems include naphthyl and isoquinolinyl. Preferred R1 groups include -halo, an optionally substituted Cι-6 aliphatic group, phenyl, -COR6, -OR6, -CN, -S02R6, -S02NH2, -N(R6)2, -C02R6, -CONH2, -NHCOR6, -OC(0)NH2, or -NHS02R6. When R1 is an optionally substituted d_6 aliphatic group, the most preferred optional substituents are halogen. Examples of preferred R1 groups include -CF3, -Cl, -F, -CN, -COCH3, -OCH3, -OH, -CH2CH3, -OCH2CH3, -CH3, -CF2CH3, cyclohexyl, t-butyl, isopropyl, cyclopropyl, -C≡CH, -C≡C-CH3, -S02CH3, -S02NH2, -N(CH3)2, -C02CH3, -CONH2, -NHCOCHa, -OC(0)NH2, -NHS02CH3, and -OCF3.
On Ring C preferred R5 substituents, when present, include -halo, -CN, -N02, -N(R4)2, optionally substituted d_s aliphatic group, -OR, -C(0)R, -C02R, -CONH(R4), -N(R4)COR, -S02N(R4)2, and -N (R4) S02R. More preferred R5 substituents include -Cl, -F, -CN, -CF3, -NH2, -NH(Ci_4 aliphatic), -N(d_4 aliphatic)2, -0(Cι-4 aliphatic), d_4 aliphatic, and -C0 (CX-4 aliphatic). Examples of such preferred R5 substituents include -Cl, -F, -CN, -CF3, -NH2, -NHMe, -NMe2, -OEt, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, and -C02Et.
When G is Ring D, preferred formula VIII Ring D monocyclic rings include substituted and unsubstituted phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, thienyl, azepanyl, and morpholinyl rings. When two adjacent substituents on Ring D are taken together to form a fused ring, the Ring D system is bicyclic. Preferred formula VIII Ring D bicyclic rings include 1, 2 , 3 , 4 -tetrahydroisoquinolinyl, 1,2,3,4- tetrahydroquinolinyl, 2, 3-dihydro-lff-isoindolyl, 2,3- dihydro-Iff-indolyl, isoquinolinyl, quinolinyl, and naphthyl . Examples of more preferred bicyclic Ring D systems include naphthyl and isoquinolinyl.
Preferred R5 substituents on Ring D of formula VIII include halo, oxo, CN, -N02, -N(R4)2, -C02R, -CONH(R4), -N(R4)C0R, -S02N(R)2, -N(R4)S02R, -SR, -OR, -C(0)R, or substituted or unsubstituted group selected from 5-6 membered heterocyclyl, C6-ιo aryl, or d-6 aliphatic. More preferred R5 substituents include -halo, -CN, -oxo, -SR, -OR, -N(R4)2, -C(0)R, or a substituted or unsubstituted group selected from 5-6 membered heterocyclyl, C6-ιo aryl, or d-6 aliphatic. Examples of Ring D substituents include -OH, phenyl, methyl, CH20H, CH2CH2OH, pyrrolidinyl, OPh, CF3, C≡CH, Cl, Br, F, I, NH2, C(0)CH3, i-propyl, tert-butyl, SEt, OMe, N(Me)2, methylene dioxy, and ethylene dioxy.
Preferred formula VIII compounds have one or more, and more preferably all, of the features selected from the group consisting of:
(a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is selected from a naphthyl, quinolinyl or isoquinolinyl ring, and R1 is -halo, an optionally substituted d-6 aliphatic group, phenyl, -COR6, -OR6, -CN, -S02R6, -S02NH2, -N(R6)2, -C0R6, -C0NH2, -NHCOR6, -0C(0)NH2, or -NHS02R6; or Ring D is an optionally substituted ring selected from a phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, thienyl, azepanyl, morpholinyl, 1,2,3,4- tetrahydroisoquinolinyl, 1, 2, 3, -tetrahydroquinolinyl, 2, 3 -dihydro-Iff-isoindolyl, 2, 3 -dihydro-Iff-indolyl, isoquinolinyl, quinolinyl, or naphthyl ring; (b) Rx is T-R3 wherein T is a valence bond or a methylene; and
(c) R2' is hydrogen and R2 is hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a Cι_6 aliphatic group, or R2 and R2' are taken together with their intervening atoms to form a substituted or unsubstituted benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring.
More preferred compounds of formula VIII have one or more, and more preferably all, of the features selected from the group consisting of:
(a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is a naphthyl ring, and R1 is -halo, a Cι_6 haloaliphatic group, a Cι-6 aliphatic group, phenyl, or -CN; or Ring D is an optionally substituted ring selected from phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, morpholinyl, 1,2, 3, 4 -tetrahydroisoquinolinyl, 1,2,3,4- tetrahydroquinolinyl, 2 , 3-dihydro-lff-isoindolyl, 2,3- dihydro-Iff-indolyl, isoquinolinyl, quinolinyl, or naphthyl ; .
(b) Rx is T-R3 wherein T is a valence bond or a methylene and R3 is CN, -R or -OR;
(c) R2' is hydrogen and R2 is hydrogen or a substituted or unsubstituted group selected from aryl, or a Cχ-6 aliphatic group, or R2 and R2' are taken together with their intervening atoms to form a substituted or unsubstituted benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring; and
(d) each R5 is independently selected from -halo, -CN, -N02, -N(R4)2, optionally substituted Cι-6 aliphatic group, -OR, -C(0)R, -C02R, -CONH(R4), -N(R)COR, -S02N(R4)2, or -N(R4)S02R.
Even more preferred compounds of formula VIII have one or more, and more preferably all, of the features selected from the group consisting of :
(a) Rx is T-R3 wherein T is a valence bond or a methylene and R3 is -R or -OR wherein R is an optionally substituted group selected from Cι-6 aliphatic, phenyl, or a 5-6 membered heteroaryl or heterocyclyl ring; (b) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is a naphthyl ring, and R1 is -halo, a d-4 aliphatic group optionally substituted with halogen, or -CN; or Ring D is an optionally substituted ring selected from phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, morpholinyl, 1,2,3, 4-tetrahydroisoquinolinyl, 1,2,3,4- tetrahydroquinolinyl, isoquinolinyl, quinolinyl, or naphthyl ;
(c) R2 and R2' are taken together with their intervening atoms to form a benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring optionally substituted with -halo, -N(R4)2, -d-4 alkyl, -d_4 haloalkyl, -N02, -O (d-4 alkyl) , -C02 (d-4 alkyl) , -CN, -S02 (Cχ-4 alkyl) , -S02NH2, -OC(0)NH2, -NH2S02 (d_4 alkyl) , -NHC(O) (Ci-4 alkyl) , -C(0)NH2, or -CO (d-4 alkyl) , wherein the (d-4 alkyl) is a straight, branched, or cyclic alkyl group; (d) each R5 is independently selected from -Cl,
-F, -CN, -CF3, -NH2, -NH(Cι-4 aliphatic), -N(Cι-4 aliphatic)2, -0(d-4 aliphatic), C1-4 aliphatic, and -C0 (d_4 aliphatic); and (e) R9 is R, OR, or N(R4)2.
Representative compounds of formula VIII are set forth in Table 7 below.
Table 7.
VIII-4 VIII-5 VIII-6
VIII-7 VIII-8 VIII-9
VIII-10 VIII-11 VIII-12
VIII-13 VIII-14 VIII-15
VIII-16 -17 VIII-1J
VIII-19 VIII-20 VIII-21
VIII-22 VIII-23 VIII-24
VIII-25 VIII-26 VIII-27
-28 -29 -30
VIII-31 VIII-32 VIII-33
VIII-34 VIII-35 VIII-36
VIII-37 VIII-38 VIII-39
VIII-40 VIII-41 VIII-42
VIII-43 VIII-44 VIII-45
-46 VIII-47 VIII-48
VIII - 52 VIII- 53 VIII- 54
In another embodiment, this invention provides a composition comprising a compound of formula VIII and a pharmaceutically acceptable carrier. One aspect of this invention relates to a method of inhibiting GSK-3 activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula VIII. Another aspect relates to a method of treating a disease that is alleviated by treatment with a GSK-3 inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula VIII. Another aspect relates to a method of enhancing glycogen synthesis and/or lowering blood levels of glucose in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula VIII. This method is especially useful for diabetic patients.
Another aspect relates to a method of inhibiting the production of hyperphosphorylated Tau protein in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula VIII. This method is especially useful in halting or slowing the progression of Alzheimer's disease. Another aspect relates to a method of inhibiting the phosphorylation of β-catenin in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula VIII. This method is especially useful for treating schizophrenia. One aspect of this invention relates to a method of inhibiting Aurora activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula VIII. Another aspect relates to a method of treating a disease that is alleviated by treatment with an Aurora inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula VIII . This method is especially useful for treating cancer, such as colon, ovarian, and breast cancer. One aspect of this invention relates to a method of inhibiting CDK-2 activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula VIII. Another aspect relates to a method of treating a disease that is alleviated by treatment with a CDK-2 inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula VIII. This method is especially useful for treating cancer, Alzheimer's disease, restenosis, angiogenesis, glomerulonephritis, cytomegalovirus, HIV, herpes, psoriasis, atherosclerosis, alopecia, and autoimmune diseases such as rheumatoid arthritis.
Another method relates to inhibiting GSK-3, Aurora, or CDK-2 activity in a biological sample, which method comprises contacting the biological sample with the GSK-3 or Aurora inhibitor of formula VIII, or a pharmaceutical composition thereof, in an amount effective to inhibit GSK-3, Aurora or CDK-2.
Each of the aforementioned methods directed to the inhibition of GSK-3, Aurora or CDK-2, or the treatment of a disease alleviated thereby, is preferably carried out with a preferred compound of formula VIII, as described above.
The above formula I compounds contain a pyrazole ring bearing the R2 and R2' substituents. In their search for further inhibitors of the protein kinases GSK and Aurora, applicants sought to replace the pyrazole moiety of formula I with other heteroaromatic rings . One of the more effective pyrazole ring replacements was found to be a triazole ring. Inhibitors having this triazole ring are otherwise structurally similar to the formula I compounds and are represented by the general formula IX:
IX
or a pharmaceutically acceptable derivative or prodrug thereof , wherei : Z1 is nitrogen or CR9 and Z2 is nitrogen or CH, provided that at least one of Z1 and Z2 is nitrogen; G is Ring C or Ring D;
Ring C is selected from a phenyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, or 1, 2, 4-triazinyl ring, wherein said Ring C has one or two ortho substituents independently selected from -R1, any substitutable non- ortho carbon position on Ring C is independently substituted by -R5, and two adjacent substituents on Ring C are optionally taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-6 membered ring having 0-3 heteroatoms selected from oxygen, sulfur or nitrogen, said fused ring being optionally substituted by halo, oxo, or -R8;
Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein Ring D is substituted at any substitutable ring carbon by oxo or -R5, and at any substitutable ring nitrogen by -R4, provided that when Ring D is a six-membered aryl or heteroaryl ring, -R5 is hydrogen at each ortho carbon position of Ring D;
R1 is selected from -halo, -CN, -N02, T-V-R6, phenyl, 5-6 membered heteroaryl ring, 5-6 membered heterocyclyl ring, or Cx-S aliphatic group, said phenyl, heteroaryl, and heterocyclyl rings each optionally substituted by up to three groups independently selected from halo, oxo, or -R8, said Ci-6 aliphatic group optionally substituted with halo, cyano, nitro, or oxygen, or R1 and an adjacent substituent taken together with their intervening atoms form said ring fused to Ring C;
Rx and Ry are independently selected from T-R3 , or Rx and Rγ are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-8 membered ring having 0-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen, wherein any substitutable carbon on said fused ring formed by Rx and Rγ is substituted by oxo or T-R3, and any substitutable nitrogen on said ring formed by Rx and Ry is substituted by R4;
T is a valence bond or a Cι_4 alkylidene chain;
R2 is -R or -T-W-R6; R3 is selected from -R, -halo, -OR, -C(=0)R, -C02R, -COCOR, -COCH2COR, -N02, -CN, -S(0)R, -S(0)2R, -SR, -N(R4)2, -CON(R7)2, -S02N(R7)2, -OC(=0)R, -N(R7)COR, -N(R7) C02 (optionally substituted Ci-6 aliphatic) , -N(R)N(R)2, -C=NN(R4)2, -C=N-OR, -N (R7) CON (R7) 2, -N(R)S02N(R7)2/ -N(R4)S02R, or -OC (=0)N (R7) 2; each R is independently selected from hydrogen or an optionally substituted group selected from Cι-6 aliphatic, C6.10 aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms ,- each R4 is independently selected from -R7, -COR7,
-C02 (optionally substituted Cι-6 aliphatic) , -CON(R7)2, or -S02R7, or two R4 on the same nitrogen are taken together to form a 5-8 membered heterocyclyl or heteroaryl ring; each R5 is independently selected from -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S{0)R, -S02R, -SR, -N(R4)2, -CON(R )2, -S02N(R4)2, -OC(=0)R, -N(R4)COR, -N(R4) C02 (optionally substituted Cι_6 aliphatic) , -N(R4)N(R)2, -C=NN(R )2, -C=N-0R, -N (R4) CON (R4) _ ,
-N(R4)S02N(R4)2, -N(R)S02R, or -OC (=0)N(R4) 2, or R5 and an adjacent substituent taken together with their intervening atoms form said ring fused to Ring C;
V is -0-, -S-, -SO-, -S02-, -N(R6)S02-, -S02N(R6)-, -N(R6)-, -CO-, -C02-, -N(R6)CO-, -N (R6) C (0) O- , -N(R6)CON(R6) -, -N(R6)S02N(R6) -, -N (Rε)N (R6) - , -C(0)N(R6)-, -OC(0)N(R6)-, -C(R6)20-, -C(R6)2S-, -C(Rs)2SO-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C (R6) 2N (R6) - , -C(Rε)2N(R6)C(0) -, -C(R6)2N(R6)C(0)0-, -C (R6) =NN(R6) - , -C(R6)=N-0-, -C(R6)2N(R5)N(R6) -, -C (Re) 2N (R6) S02N (R6) - , or -C(R6)2N(R6)CON(R6)-; W is -C(R6)20-, -C(R6)2S-, -C(R6)2SO-, -C(R6)2S02-, -C(Rε)2S02N(R6)-, -C(R6)2N(R6)-, -CO-, -C02-, -C(R6)OC(0) -, -C(R6)OC(0)N(R6) -, -C (R6) 2N(R6) CO- , -C(Rε)2N(R6)C(0)0-, -C(R6)=NN(R6)-, -C(Rε)=N-0-, -C(R6)2N(R6)N(R6) -, -C(Rε)2N(R6)S02N(R6) -, -C(R6)2N(R6)CON(R6) -, or -CON(R6)-; each R6 is independently selected from hydrogen, an optionally substituted Cι_4 aliphatic group, or two R6 groups on the same nitrogen atom are taken together with the nitrogen atom to form a 5-6 membered heterocyclyl or heteroaryl ring; each R7 is independently selected from hydrogen or an optionally substituted C_-6 aliphatic group, or two R7 on the same nitrogen are taken together with the nitrogen to form a 5-8 membered heterocyclyl or heteroaryl ring; each R8 is independently selected from an optionally substituted d-4 aliphatic group, -OR6, -SR6, -COR6, -S02R6, -N(R6)2, -N(Rε)N(Rε)2, -CN, -N02, -CON(R6)2, or -C02R6; and
R9 is selected from -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R)2, -CON(R4)2, -S02N(R4)2/ -OC(=0)R, -N(R)C0R, -N(R4) C02 (optionally substituted d-6 aliphatic) , -N(R4)N(R4) 2, -C=NN(R4)2, -C=N-0R, -N(R4)C0N(R4)2, -N(R4) S02N(R4) 2, -N(R4)S02R, or -0C(=0)N(R4)2.
Compounds of formula IX may exist in alternative tautomeric forms, as in tautomers 1-3 shown below. Unless otherwise indicated, the representation of any of these tautomers is meant to include the other two.
The Rx and Rγ groups of formula IX may be taken together to form a fused ring, providing a bicyclic ring system containing Ring A. Preferred R^/R rings include a 5-, 6-, 7-, or 8-membered unsaturated or partially unsaturated ring having 0-2 heteroatoms, wherein said Rx/Ry ring is optionally substituted. Examples of Ring A systems are shown below by compounds IX-A through IX-DD, wherein Zα is nitrogen or C(R9) and Z2 is nitrogen or C(H).
IX-G IX-H IX-I
IX-M IX-N IX-0
IX-P IX-Q IX-R
IX- s IX-T IX-ϋ
IX-V IX-W IX-X
IX-Y IX- z IX-AA
IX-BB IX-CC IX-DD
Preferred bicyclic Ring A systems of formula IX include IX-A, IX-B, IX-C, IX-D, IX-E, IX-F, IX-G, IX-H, IX-I, IX-J, IX-K, IX-L, and IX-M, more preferably IX-A,
IX-B, IX-C, IX-F, and IX-H, and most preferably IX-A, IX- B, and IX-H.
In the monocyclic Ring A system of formula IX, preferred Rx groups include hydrogen, alkyl- or dialkylamino, acetamido, or a Cχ-4 aliphatic group such as methyl, ethyl, cyclopropyl, isopropyl or t-butyl. Preferred Ry groups, when present, include T-R3 wherein T is a valence bond or a methylene, and R3 is -R, -N(R)2, or -OR. Examples of preferred Rγ include 2-pyridyl, 4- pyridyl, piperidinyl, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, alkyl- or dialkylamino, acetamido, optionally substituted phenyl such as phenyl or halo- substituted phenyl, and methoxymethyl . In the bicyclic Ring A system of formula IX, the ring formed by Rx and Rγ taken together may be substituted or unsubstituted. Suitable substituents include -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -CON(R4)2, -S02N(R)2,
-OC(=0)R, -N(R4)COR, -N(R4)C02 (optionally substituted d_6 aliphatic), -N(R4)N(R4) _ , -C=NN(R4)2, -C=N-0R, -N(R4)CON(R4)2, -N(R)S02N(R)2, -N(R4)S02R, or -OC(=0)N(R) , wherein R and R4 are as defined above. Preferred Rx/Rγ ring substituents include -halo, -R, -OR, -COR, -C02R, -C0N(R4)2, -CN, or -N(R4)2 wherein R is an optionally substituted Cι-6 aliphatic group.
Preferred R2 groups of formula IX include hydrogen, d-4 aliphatic, alkoxycarbonyl, (un) substituted phenyl, hydroxyalkyl, alkoxyalkyl, aminocarbonyl, mono- or dialkylaminocarbonyl, aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl, phenylaminocarbonyl, and (N- heterocyclyl) carbonyl . Examples of such preferred R2 substituents include methyl, cyclopropyl, ethyl, isopropyl, propyl, t-butyl, cyclopentyl, phenyl, C02H, C02CH3, CH2OH, CH20CH3, CH2CH2CH2OH, CH2CH2CH2OCH3 , CH2CH2CH2OCH2Ph, CH2CH2CH2NH2 , CH2CH2CH2NHCOOC (CH3) 3 , CONHCH(CH3)2, CONHCH2CH=CH2, CONHCH2CH2OCH3 , CONHCH2Ph, CONH (eyelohexyl) , CON(Et)2, CON (CH3) CH2Ph, CONH (n-C3H7) , CON(Et)CH2CH2CH3, CONHCH2CH (CH3) 2, CON (n-C3H7) _ , CO (3- methoxymethylpyrrolidin-1-yl) , CONH (3 -tolyl) , CONH (4- tolyl) , CONHCH3, CO (morpholin-1-yl) , CO (4-methylpiperazin- l-yl) , CONHCH2CH2OH, CONH2, and CO (piperidin-1-yl) . A more preferred R2 group for formula IX compounds is hydrogen.
An embodiment that is particularly useful for treating GSK3-mediated diseases relates to compounds of formula X wherein ring A is a pyrimidine ring:
or a pharmaceutically acceptable derivative or prodrug thereof, wherein; Ring C is selected from a phenyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, or 1, 2, 4-triazinyl ring, wherein said Ring C has one or two ortho substituents independently selected from -R1, any substitutable non- ortho carbon position on Ring C is independently substituted by -R5, and two adjacent substituents on Ring C are optionally taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-6 membered ring having 0-3 heteroatoms selected from oxygen, sulfur or nitrogen, said fused ring being optionally substituted by halo, oxo, or -R8; R1 is selected from -halo, -CN, -N02, T-V-R6, phenyl, 5-6 membered heteroaryl ring, 5-6 membered heterocyclyl ring, or Ci-6 aliphatic group, said phenyl, heteroaryl, and heterocyclyl rings each optionally substituted by up to three groups independently selected from halo, oxo, or -R8, said d_6 aliphatic group optionally substituted with halo, cyano, nitro, or oxygen, or R1 and an adjacent substituent taken together with their intervening atoms form said ring fused to.Ring C; Rx and Ry are independently selected from T-R3, or Rx and Rγ are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-8 membered ring having 0-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen, wherein any substitutable carbon on said fused ring formed by Rx and Ry is substituted by oxo or T-R3 , and any substitutable nitrogen on said ring formed by Rx and Rγ is substituted by R4,-
T is a valence bond or a d-4 alkylidene chain;
R2 is -R or -T-W-R6;
R3 is selected from -R, -halo, -OR, -C(=0)R, -C0R, -COCOR, -COCH2COR, -N02, -CN, -S(0)R^ -S(0)2R, -SR, -N(R4)2, -CON(R7)2, -S02N(R7)2, -OC(=0)R, -N(R7)C0R, -N(R7) C02 (optionally substituted Cα-6 aliphatic) , -N(R)N(R4)2, -C=NN(R4)2, -C=N-0R, -N(R7) CON(R7) 2, -N(R7)S02N(R7)2, -N(R)S02R, or -OC (=0)N(R7) 2; each R is independently selected from hydrogen or an optionally substituted group selected from Cι-6 aliphatic, C6-ιo aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms ; each R4 is independently selected from -R7, -COR7,
-C02 (optionally substituted Cι-6 aliphatic) , -C0N(R7)2, or -S02R7, or two R4 on the same nitrogen are taken together to form a 5-8 membered heterocyclyl or heteroaryl ring; each R5 is independently selected from -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -C0N(R4)2, -S02N(R)2, -OC(=0)R, -N(R4)COR, -N(R4) C02 (optionally substituted d-6 aliphatic) , -N(R )N(R4)2, -C=NN(R4)2, -C=N-OR, -N(R4) CON (R4) _ , -N(R4)S02N(R4)2, -N(R4)S02R, or -OC (=0)N(R4) ■_ , or R5 and an adjacent substituent taken together with their intervening atoms form said ring fused to Ring C; V is -0-, -S-, -SO-, -SO2-, -N(R6)S02-, -S02N(R6)-, -N(R6)-, -CO-, -C02-, -N(R6)CO-, -N (R6) C (0) O- , -N(R6)CON(R6) -, -N(R6)S02N(R6) -, -N (Rε) N (R6) - ,
-C(0)N(R6)-, -OC(0)N(R6)-, -C(R6)20-, -C(R6)2S-, -C(R6)2SO-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C (R6) 2N (R6) - , -C(R6)2N(R6)C(0) -, -C(R6)2N(R6)C(0)0-, -C (R6) =NN (Rε) - , -C(R6)=N-0-, -C(R6)2N(Rε)N(R6)-, -C (R6) 2N (Rε) S02N (R6) - , or -C(R6)2N(R6)CON(R6) -;
W is -C(Rε)20-, -C(R6)2S-, -C(R6)2SO-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C(Rε)2N(R6)-, -CO-, -C02-, -C(R6)0C(0) -, -C(R6)OC(0)N(R6) -, -C (R6) 2N(R6) CO- , -C(Rε)2N(R6)C(0)0-, -C(Rε)=NN(R6)-, -C(R6)=N-0-, -C(R6)2N(R6)N(R6) -, -C (R6) 2N(R6) S02N(Rs) - , -C(R6)2N(R6)CON(R6) -, or -CON(R6)-; each Rε is independently selected from hydrogen, an optionally substituted C1-4 aliphatic group, or two R6 groups on the same nitrogen atom are taken together with the nitrogen atom to form a 5-6 membered heterocyclyl or heteroaryl ring; each R7 is independently selected from hydrogen or an optionally substituted Cι~6 aliphatic group, or two R7 on the same nitrogen are taken together with the nitrogen to form a 5-8 membered heterocyclyl or heteroaryl ring; and each R8 is independently selected from an optionally substituted C1-4 aliphatic group, -OR6, -SR6, -COR6, -S02R6, -N(R6)2, -N(R6)N(R6)2, -CN, -N02, -CON(Rs)2/ or -C02R6.
Compounds of formula X are structurally similar to compounds of formula II except, for the replacement of the pyrazole ring moiety by the triazole ring moiety. Preferred R2, R , Rγ and Ring C groups of formula X are as described above for the formula II compounds . Preferred formula X compounds have one or more,' and more preferably all, of the features selected from the group consisting of:
(a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is selected from a naphthyl, quinolinyl or isoquinolinyl ring;
(b) Rx is hydrogen or Ci-4 aliphatic and Rγ is T- R3, or Rx and Rγ are taken together with their intervening atoms to form an optionally substituted 5-7 membered unsaturated or partially unsaturated ring having 0-2 ring nitrogens;
(c) Rα is -halo, an optionally substituted Ci-6 aliphatic group, phenyl, -COR6, -OR6, -CN, -S02Rε, -S02NH2, -N(R6)2, -C02Rε, -CONH2/ -NHCOR6, -0C(0)NH2, or -NHS02R6; and (d) R2 is hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a Ci-e aliphatic group.
More preferred compounds of formula X have one or more, and more preferably all, of the features selected from the group consisting of:
(a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is a naphthyl ring; (b) Rx is hydrogen or methyl and Ry is -R,
N(R4)2, or -OR, or Rx and Rγ are taken together with their intervening atoms to form a benzo ring or a 5-7 membered carbocyclo ring, wherein said ring formed by Rx and Ry is optionally substituted with -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -C0N(R4)2, -S02N(R4)2, -OC(=0)R, -N(R4)COR, -N(R4) C02 (optionally substituted Ci-6 aliphatic) , -N(R4)N(R4) _ , -C=NN(R4)2, -C=N-OR, -N(R4)CON(R4)2, -N (R4) S02N (R4) _ , -N(R4)S02R, or -OC(=0)N(R4)2;
(c) R1 is -halo, a d-6 haloaliphatic group, a d_ 6 aliphatic group, phenyl, or -CN;
(d) R2 is hydrogen or a substituted or unsubstituted group selected from aryl or a Cι-6 aliphatic group ; and
(e) each R5 is independently selected from -halo, -CN, -N02, -N(R )2, optionally substituted d_6 aliphatic group, -OR, -C(0)R, -C02R, -CONH(R4), -N(R4)COR, -S02N(R4)2, or -N(R4)S02R.
Even more preferred compounds of formula X have one or more, and more preferably all, of the features selected from the group consisting of :
(a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is a naphthyl ring;
(b) • Rx is hydrogen or methyl and Rγ is methyl, methoxymethyl , ethyl, cyclopropyl, isopropyl, t-butyl, alkyl- or an optionally substituted group selected from
2-pyridyl , 4-pyridyl, piperidinyl, or phenyl, or Rx and Rγ are taken together with their intervening atoms to form an optionally substituted benzo ring or a 6-membered carbocyclo ring; (c) R1 is -halo, a Ci-4. aliphatic group optionally substituted with halogen, or -CN;
(d) R2 is hydrogen or a Cι_6 aliphatic group; and (e) each Rs is independently selected from -Cl, -F, -CN, -CF3, -NH2, -NH(Ci-4 aliphatic), -N(Cι-4 aliphatic) 2, -0(Cι_4 aliphatic), d-4 aliphatic, and -C02(d-4 aliphatic). Another embodiment of this invention relates to compounds of formula XI :
XI
or a pharmaceutically acceptable derivative or prodrug thereof, wherein:.
Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein Ring D is substituted at any substitutable ring carbon by oxo or -R5, and at any substitutable ring nitrogen by -R4, provided that when Ring D is a six-membered aryl or heteroaryl ring, -R5 is hydrogen at each ortho carbon position of Ring D;
Rx and Ry are taken together with their intervening atoms to form a fused benzo ring or 5-8 membered carbocyclo ring, wherein any substitutable carbon on said fused ring formed by Rx and Rγ is substituted by oxo or T-R3;
T is a valence bond or a Cι-4 alkylidene chain;
R2 is -R or -T-W-R6; R3 is selected from -R, -halo, =0, -OR, -C(=0)R, -C02R, -COCOR, -COCH2COR, -N02, -CN, -S(0)R, -S(0)2R, -SR, -N(R4)2, -CON(R4)2, -S02N(R)2, -OC(=0)R, -N(R4)COR, -N(R4) C02 (optionally substituted Ci-6 aliphatic) , -N(R4)N(R4)2, -C=NN(R)2, -C=N-OR, -N (R4) CON (R4) 2, -N(R4)S02N(R4)2, -N(R)S02R, or -OC (=0)N(R4) 2; each R is independently selected from hydrogen or an optionally substituted group selected from Cχ-6 aliphatic, C6-ιo aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms ; each R4 is independently selected from -R7, -COR7,
-C02 (optionally substituted Cι-6 aliphatic) , -CON(R7)2, or -S02R7, or two R4 on the same nitrogen are taken together to form a 5-8 membered heterocyclyl or heteroaryl ring; each R5 is independently selected from -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -CON(R4)2, -S02N(R4)2, -OC(=0)R, -N(R)COR, -N(R4) C02 (optionally substituted Ci-6 aliphatic) , -N(R4)N(R4)2, -C=NN(R4)2, -C=N-OR, -N(R4) C0N(R4) 2, -N(R4)S02N(R4)2, -N(R4)S02R, or -OC (=0)N(R4) 2;
V is -0-, -S-, -SO-, -S02-, -N(R6)S02-, -S02N(R6)-, -N(R6)-, -CO-, -C02-, -N(R6)CO-, -N(R6) C (0) O- , -N(R6)CON(R6) -, -N(Rε)S02N(R6) -, -N (Rε) N(R6) - ,
-C(0)N(R6)-, -OC(0)N(R6)-, -C(R6)20-, -C(R6)2S-, -C(R6)2SO-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C (R6) 2N (R6) - , -C(R6)2N(R6)C(0) -, -C(R6)2N(R6)C(0)0-, -C (R6) =NN(R6) - , -C(R6)=N-0-, -C(Re)2N(Rε)N(R6) -, -C (Rε) 2N(R6) S02N(R6) - , or -C(Rε)2N(R6)CON(R6)-;
W is -C(R6)20-, -C(R6)2S-, -C(Rε)2SO-, -C(Rε)2S02-, -C(R6)2S02N(R6)-, -C(R6)2N(R6)-, -CO-, -C02-, -C(R6)OC(0) -, -C(R6)0C(0)N(R6) -, -C (R6) 2N(Rε) CO- , -C(R6)2N(R6)C(0)0-, -C(R6)=NN(R6) -, -C(Rε)=N-0-, -C(R6)2N(Rε)N(R6) -, -C(R6)2N(R6)S02N(R6)-, -C(Rs)2N(Rε)C0N(Rε) -, or -CON(R6)-; each R6 is independently selected from hydrogen or an optionally substituted Cχ-4 aliphatic group, or two R6 groups on the same nitrogen atom are taken together with the nitrogen atom to form a 5-6 membered heterocyclyl or heteroaryl ring; and each R7 is independently selected from hydrogen or an optionally substituted Cχ-6 aliphatic group, or two R7 on the same nitrogen are taken together with the nitrogen to form a 5-8 membered heterocyclyl or heteroaryl ring.
Compounds of formula XI are structurally similar to compounds of formula III except for the replacement of the pyrazole ring moiety by the triazole ring moiety. Preferred R2, Rx, Rγ, and Ring D groups of formula XI are as described above for the formula III compounds . Preferred formula XI compounds have one or more, and more preferably all, of the features selected from the group consisting of :
(a) Ring D is an optionally substituted ring selected from a phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, thienyl, azepanyl, morpholinyl, 1, 2, 3 , 4-tetrahydroisoquinolinyl, 1,2,3,4- tetrahydroquinolinyl, 2 , 3-dihydro-lH-isoindolyl, 2,3- dihydro-li-"-indolyl, isoquinolinyl, quinolinyl, or naphthyl ring;
(b) Rx and Rγ are taken together with their intervening atoms to form an optionally substituted benzo ring or 5-7 membered carbocyclo ring; and (c) R2 is hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a d-6 aliphatic group.
More preferred compounds of formula XI have one or more, and more preferably all, of the features selected from the group consisting of:
(a) Ring D is an optionally substituted ring selected from phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, morpholinyl, 1,2,3,4- tetrahydroisoquinolinyl, 1, 2 , 3 , 4-tetrahydroquinolinyl, 2 , 3-dihydro-lH-isoindolyl , 2 , 3 -dihydro-1JJ-indolyl , isoquinolinyl, quinolinyl, or naphthyl;
(b) Rx and Ry are taken together with their intervening atoms to form a benzo ring or 5-7 membered carbocyclo ring, wherein said ring formed by Rx and Rγ is optionally substituted with -R, oxo, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -CON(R4)2, -S02N(R4)2, -0C(=0)R, -N(R4)C0R, -N(R4) C02 (optionally substituted Cι_6 aliphatic) , -N(R4)N(R4)2, -C=NN(R4)2, -C=N-0R, -N(R4) CON(R4) 2, -N(R4)S02N(R4)2, -N(R4)S02R, or -OC (=0)N(R4) 2;
(c) R2 is hydrogen or a substituted or unsubstituted group selected from aryl or a d-s aliphatic group; and (d) each R5 is independently selected from halo, oxo, CN, N02, -N(R4)2, -C02R, -CONH(R4), -N(R4)COR, -S02N(R4)2, -N(R4)S02R, -SR, -OR, -C(0)R, or a substituted or unsubstituted group selected from 5-6 membered heterocyclyl, C6-ιo aryl, or d-6 aliphatic. Even more preferred compounds of formula XI have one or more, and more preferably all, of the features selected from the group consisting of: (a) Rx and Ry are taken together with their intervening atoms to form a benzo ring or 6-membered carbocyclo ring, wherein said ring formed by Rx and Ry is optionally substituted with halo, CN, oxo, Ci-6 alkyl, d-6 alkoxy, (d_6 alkyl) carbonyl, (d-6 alkyl) sulfonyl, mono- or dialkylamino, mono- or dialkylaminocarbonyl, mono- or dialkylaminocarbonyloxy, or 5-6 membered heteroaryl;
(b) each R5 is independently selected from -halo, -CN, -oxo, -SR, -OR, -N(R)2, -C(0)R, or a substituted or unsubstituted group selected from 5-6 membered heterocyclyl, Cε-io aryl, or d-6 aliphatic; and
(c) R2 is hydrogen or a Cι-S aliphatic group. Another embodiment of this invention relates to compounds of formula XII :
XII
or a pharmaceutically acceptable derivative or prodrug thereof, wherein: Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein Ring D is substituted at any substitutable ring carbon by oxo or -R5, and at any substitutable ring nitrogen by -R4, provided that when Ring D is a six-membered aryl or heteroaryl ring, -R5 is hydrogen at each ortho carbon position of Ring D; Rx and Rγ are independently selected from T-R3, or Rx and Rγ are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-8 membered ring having 1-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen, wherein any substitutable carbon on said fused ring is optionally and independently substituted by T-R3, and any substitutable nitrogen on said ring is substituted by R4;
T is a valence bond or a d-4 alkylidene chain;
R2 is -R or -T-W-R6;
R3 is selected from -R, -halo, =0, -OR, -C(=0)R, -C02R,
-COCOR, -C0CH2C0R, -N02, -CN, -S(0)R, -S(0)2R, -SR, -N(R4)2, -CON(R4)2, -S02N(R)2, -OC(=0)R, -N(R4)C0R, -N(R4) C02 (optionally substituted Ci-6 aliphatic) , -N(R4)N(R4)2, -C=NN(R4)2, -C=N-OR, -N (R4) CON (R4) _ , -N(R4)S02N(R)2, -N(R4)S02R, or -OC (=0) N (R4) 2; each R is independently selected from hydrogen or an optionally substituted group selected from Q_.6 aliphatic, C6-ιo aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms ; each R4 is independently selected from -R7, -COR7, -C02 (optionally substituted d_6 aliphatic) , -CON(R7)2, or -S02R7, or two R4 on the same nitrogen are taken together to form a 5-8 membered heterocyclyl or heteroaryl ring; each R5 is independently selected from -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -C0N(R4)2, -S02N(R)2, -OC(=0)R, -N(R4)COR, -N(R4) C02 (optionally substituted d-6 aliphatic) , -N(R )N(R4)2, -C=NN(R4)2, -C=N-OR, -N (R4) CON (R4) _, -N(R4)S02N(R4)2, -N(R4)S02R, or -OC (=0) N(R4) 2; V is -0-, -S-, -SO-, -S02-, -N(R6)S02-, -S02N(R6)-, -N(R6) -, -CO-, -CO2-, -N(R6)C0-, -N(R6)C(0)0-, -N(R6)C0N(Rε) -, -N(R )S02N(Rε) -, -N (R6) N (R6) - ,
-C(0)N(R6) -, -OC(0)N(R6)-, -C(R6)20-, -C(Rδ)2S-, -C(R6)2SO-, -C(R6)2S02-, -C(R6)2S02N(R6) -, -C (R6) 2N (R6) - , -C(Re)2N(R6)C(0) -, -C(R6)2N(R6)C(0)0-, -C (R6) =NN(Rε) - , -C(R6)=N-0-, -C(Rε)2N(Rε)N(R6) -, -C (R6) 2N(R6) S02N(R6) - , or -C(R6)2N(R6)CON(Rε) -;
W is -C(R6)20-, -C(R6)2S-, -C(R6)2SO-, -C(R6)2S02-, -C(Rδ)2S02N(Rε) -, -C(R6)2N(R6)-, -CO-, -C02-, -C(Rε)OC(0) -, -C(Rε)OC(0)N(R6) -, -C (R6) 2N(R6) CO- , -C(Rε)2N(R6)C(0)0-, -C(Rε)=NN(Rε) -, -C (R6) =N-0- , -C(R6)2N(R6)N(R6)-, -C (R6) 2N (Rε) S02N (Rε) - , -C(Rε)2N(R6)CON(R6) -, or -CON(R6)-; each R6 is independently selected from hydrogen or an optionally substituted C1- aliphatic group, or two R6 groups on the same nitrogen atom are taken together with the nitrogen atom to form a 5-6 membered heterocyclyl or heteroaryl ring; and each R7 is independently selected from hydrogen or an optionally substituted Cι_6 aliphatic group, or two R7 on the same nitrogen are taken together with the nitrogen to form a 5-8 membered heterocyclyl ring or heteroaryl .
Compounds of formula XII are structurally similar to compounds of formula IV except for the replacement of the pyrazole ring moiety by the triazole ring moiety. Preferred R2, Rx, Rγ, and Ring D groups of formula XII are as described above for the formula IV compounds . Preferred formula XII compounds have one or more, and more preferably all, of the features selected from the group consisting of :
(a) Ring D is an optionally substituted ring selected from a phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, thienyl, azepanyl, morpholinyl, 1, 2, 3 , 4-tetrahydroisoquinolinyl, 1,2,3,4- tetrahydroquinolinyl, 2, 3-dihydro-Iff-isoindolyl, 2,3- dihydro-Iff-indolyl, isoquinolinyl, quinolinyl, or naphthyl ring; (b) Rx is hydrogen or Cι- aliphatic and Rγ is T-
R3, or Rx and Rγ are taken together with their intervening atoms to form an optionally substituted 5-7 membered unsaturated or partially unsaturated ring having 1-2 ring heteroatoms ; and (c) R2 is hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a
C_.6 aliphatic group.
More preferred compounds of formula XII have one or more, and more preferably all, of the features selected from the group consisting of:
(a) Ring D is an optionally substituted ring selected from phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, morpholinyl, 1,2,3,4- tetrahydroisoquinolinyl , 1,2,3,4-tetrahydroqumolinyl , 2, 3 -dihydro-Iff- isoindolyl, 2, 3 -dihydro-Iff- indolyl, isoquinolinyl, quinolinyl, or naphthyl;
(b) Rx is hydrogen or methyl and Ry is -R, N(R )2, or -OR, or Rx and Rγ are taken together with their intervening atoms to form a 5-7 membered unsaturated or partially unsaturated ring having 1-2 ring nitrogens, wherein said ring is optionally substituted with -R, halo, oxo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -CON(R4)2, -S02N(R4)2, -OC(=0)R, -N(R4)COR, -N(R4)C02 (optionally substituted d-6 aliphatic) , -N(R4)N(R4)2, -C=NN(R4)2, -C=N-OR, -N (R4) CON (R4) _ , -N(R)S02N(R4)2, -N(R4)S02R, or -OC (=0) N (R4) 2;
(c) R2 is hydrogen or a substituted or unsubstituted group selected from aryl or a Cι-6 aliphatic grou ; and
(d) each R5 is independently selected from halo, oxo, CN, N02, -N(R4)2, -C02R, -CONH(R4), -N(R4)COR, -S02N(R4)2, -N(R4)S02R, -SR, -OR, -C(0)R, or a substituted or unsubstituted group selected from 5-6 membered heterocyclyl, C6-ιo aryl, or Ci-6 aliphatic.
Even more preferred compounds of formula XII have one or more, and more preferably all, of the features selected from the group consisting of: (a) Rx and Rγ are taken together with their intervening atoms to form a 6-membered unsaturated or partially unsaturated ring having 1-2 ring nitrogens, optionally substituted with halo, CN, oxo, Ci-6 alkyl, d_G alkoxy, (Cι-6 alkyl) carbonyl, (Cι-6 alkyl) sulfonyl, mono- or dialkylamino, mono- or dialkylaminocarbonyl, mono- or dialkylaminocarbonyloxy, or 5-6 membered heteroaryl;
(b) each R5 is independently selected from -halo, -CN, -oxo, -SR, -OR, -N(R)2, -C(0)R, or a substituted or unsubstituted group selected from 5-6 membered heterocyclyl, C6_ι0 aryl, or Ci-β aliphatic; and
(c) R2 is hydrogen or a d_6 aliphatic group. Another embodiment of this invention relates to compounds of formula XIII:
XIII
or a pharmaceutically acceptable derivative or prodrug thereof, wherein:
Z1 is nitrogen, CRa, or CH, and Z2 is nitrogen or CH; provided that one of Z1 and Z2 is nitrogen;
G is Ring C or Ring D;
Ring C is selected from a phenyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, or 1, 2, 4-triazinyl ring, wherein said Ring C has one or two ortho substituents independently selected from -R1, any substitutable non- ortho carbon position on Ring C is independently substituted by -R5, and two adjacent substituents on Ring C are optionally taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-6 membered ring having 0-3 heteroatoms selected from oxygen, sulfur or nitrogen, said fused ring being optionally substituted by halo, oxo, or -R8;
Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen .or sulfur, wherein Ring D is substituted at any substitutable ring carbon by oxo or -R5, and at any substitutable ring nitrogen by -R4, provided that when Ring D is a six-membered aryl or . heteroaryl ring, -R5 is hydrogen at each ortho carbon position of Ring D;
R1 is selected from -halo, -CN, -N02, T-V-R6, phenyl, 5-6 membered heteroaryl ring, 5-6 membered heterocyclyl ring, or Ci-β aliphatic group, said phenyl, heteroaryl, and heterocyclyl rings each optionally substituted by up to three groups independently selected from halo, oxo, or -R8, said d-6 aliphatic group optionally substituted with halo, cyano, nitro, or oxygen, or R1 and an adjacent substituent taken together with their intervening atoms form said ring fused to Ring C;
Rx and Ry are independently selected from T-R3, or Rx and Rγ are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-8 membered ring having 0-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen, wherein any substitutable carbon on said fused ring formed by Rx and Rγ is substituted by oxo or T-R3, and any substitutable nitrogen on said ring formed by Rx and Ry is substituted by R4;
T is a valence bond or a d-4 alkylidene chain;
R2 is -R or -T-W-R6;
R3 is selected from -R, -halo, -OR, -C(=0)R, -C02R, -COCOR, -COCH2COR, -N02, -CN, -S(0)R, -S(0)2R, -SR, -N(R4)2, -CON(R7)2, -S02N(R7)2, -OC(=0)R, -N(R7)C0R, -N(R7) C02 (optionally substituted Cχ-6 aliphatic), -N(R4)N(R4)2, -C=NN(R4)2, -C=N-OR, -N (R7) CON (R7) 2, -N(R7)S02N(R7)2, -N(R4)S02R, or -OC (=0)N(R7) 2; each R is independently selected from hydrogen or an optionally substituted group selected from Cι_6 aliphatic, C6-ιo aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms ; each R4 is independently selected from -R7, -COR7,
-C02 (optionally substituted d_6 aliphatic) , -CON(R7)2, or -S02R7, or two R4 on the same nitrogen are taken together to form a 5-8 membered heterocyclyl or heteroaryl ring; each R5 is independently selected from -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -CON(R4)2, -S02N(R4)2, -OC(=0)R, -N(R)C0R, -N(R4) C02 (optionally substituted d_6 aliphatic) , -N(R4)N(R4)2, -C=NN(R4)2, -C=N-OR, -N (R4) CON (R4) 2,
-N(R4)S02N(R4)2, -N(R4)S02R, or -OC (=0) N(R4) _ , or R5 and an adjacent substituent taken together with their intervening atoms form said ring fused to Ring C; V is -0-, -S-, -SO-, -S02-, -N(R6)S02-, -S02N(R6)-, -N(RS)-, -CO-, -CO2-, -N(R6)CO-, -N (R6) C (0) O- , -N(R6)CON(R6) -, -N(R6)S02N(R6) -, -N (R6) N (Rε) - , -C(0)N(R6)-, -0C(0)N(Rε) -, -C(R6)20-, -C(R6)2S-, -C(Rε)2S0-, -C(R6)2S02-, -C(Rε)2S02N(R6)-, -C (R6) 2N (R6) - , -C(R6)2N(R6)C(0)-, -C(R6)2N(R6)C(0)0-, -C (R6) =NN(R6) - , -C(R6)=N-0-, -C(RS)2N(R6)N(R6) -, -C (R6) 2N (Rε) S02N(R6) - , or -C(R6)2N(R6)C0N(R6)-; W is -C(Rε)20-, -C(R6)2S-, -C(R6)2SO-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C(R6)2N(R6)-, -CO-, -C02-, -C(R6)OC(0) -, -C(R6)OC(0)N(R6) -, -C (Rε) 2N(R6) CO- , -C(R6)2N(R6)C(0)0-, -C (R6) =NN (Rε) - , -C (R6) =N-0- , -C(Rε)2N(R6)N(R6)-, -C(R6)2N(R6)S02N(R6) -, -C(R6)2N(R6)CON(R6) -, or -CON(R6)-; each R6 is independently selected from hydrogen, an optionally substituted C1-4 aliphatic group, or two R6 groups on the same nitrogen atom are taken together with the nitrogen atom to form a 5-6 membered heterocyclyl or heteroaryl ring; each R7 is independently selected from hydrogen or an optionally substituted C_.6 aliphatic group, or two R7 on the same nitrogen are taken together with the nitrogen to form a 5-8 membered heterocyclyl or heteroaryl ring; each R8 is independently selected from an optionally substituted Cι_4 aliphatic group, -OR6, -SR6, -COR6, -S02R6, -N(R6)2, -N(R6)N(R6)2, -CN, -N02, -CON(R6)2, or -C02R6; and Ra is selected from halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -CON(R4)2, -S02N(R)2, -OC(=0)R, -N(R4)COR, - (R4) C02 (optionally substituted Cx-6 aliphatic) , -N(R)N(R4) _ , -C=NN(R4)2, -C=N-OR, -N(R4)CON(R4)2, -N (R4) S02N(R4) _ , -N(R4)S02R, -0C(=0)N(R4) 2 , or an optionally substituted group selected from C_.e aliphatic, C6-ιo aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms.
Compounds of formula XIII may be represented by specifying Z1 and Z2 as shown below:
Xllla XIIlb XIIIc
Compounds of formula XIII are structurally similar to compounds of formula V except for the replacement of the pyrazole ring moiety by the triazole ring moiety. Preferred R2, Rx, Rγ, R , and Ring G groups of formula XIII are as described above for the formula V compounds . Preferred formula XIII compounds have one or more, and more preferably all, of the .features selected from the group consisting of: (a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is selected from a naphthyl, quinolinyl or isoquinolinyl ring, and R1 is -halo, an optionally substituted Cι_6 aliphatic group, phenyl, -COR6, -OR6, -CN, -S02Rε, -S02NH2, -N(R6)2, -C02R6, -CONH2, -NHCOR5, -OC(0)NH2, or -NHS02R6; or Ring D is an optionally substituted ring selected from a phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, thienyl, azepanyl, morpholinyl, 1,2,3,4- tetrahydroisoquinolinyl , 1,2,3,4-tetrahydroqumolinyl , 2, 3-dihydro-Iff-isoindolyl, 2, 3-dihydro-Iff-indolyl, isoquinolinyl, quinolinyl, or naphthyl ring;
(b) Rx is hydrogen or d-4 aliphatic and Rγ is T- R3, or Rx and Rγ are taken together with their intervening atoms to form an optionally substituted 5-7 membered unsaturated or partially unsaturated ring having 0-2 ring nitrogens ; and
(c) R2 is hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a d-6 aliphatic group.
More preferred compounds of formula XIII have one or more, and more preferably all, of the features selected from the group consisting of : (a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is a naphthyl ring, and R1 is -halo,, a -6 haloaliphatic group, a Ci-β aliphatic group, phenyl, or -CN; or Ring D is an optionally substituted ring selected from phenyl, pyridinyl, piperidinyl, piperazinyl, pyrrolidinyl, morpholinyl, ■ 1, 2, 3 ,4-tetrahydroisoquinolinyl, 1,2,3,4- tetrahydroquinolinyl, 2, 3-dihydro-lff-isoindolyl, 2,3- dihydro-Iff-indolyl, isoquinolinyl, quinolinyl, or naphthyl;
(b) Rx is hydrogen or methyl and Ry is -R, N(R4)2, or -OR, or Rx and Rγ are taken together with their intervening atoms to form a benzo ring or a 5-7 membered carbocyclo ring, wherein said ring formed by Rx and Ry is optionally substituted with -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -C0N(R4)2, -S02N(R4)2, -OC(=0)R, -N(R4)COR, -N (R4) C02 (optionally substituted Ci-6 aliphatic) , -N(R4)N(R4) 2, -C=NN(R)2, -C=N-OR, -N(R )C0N(R4)2, -N (R4) S02N (R4) 2, -N(R4)S02R, or -OC(=0)N(R4)2;
(c) R2 is hydrogen or a substituted or unsubstituted group selected from aryl, or a Cι-6 aliphatic group; and
(d) each R5 is independently selected from -halo, -CN, -N02, -N(R4)2, optionally substituted C_.6 aliphatic group, -OR, -C(0)R, -C02R, -CONH(R4), -N(R4)COR, -S02N(R4)2, or -N(R4)S02R, and, when Ring G is Ring D, Ring D is substituted by oxo or R5.
Even more preferred compounds of formula XIII have one or more, and more preferably all, of the features selected from the group consisting of: (a) Rx is hydrogen or methyl and Rγ is methyl, methoxymethyl , ethyl, cyclopropyl, isopropyl, t-butyl, alkyl- or an optionally substituted group selected from 2-pyridyl, 4-pyridyl, piperidinyl, or phenyl, or Rx and Rγ are taken together with their intervening atoms to form a benzo ring or a 6-membered carbocyclo ring wherein said ring formed by Rx and Rγ is optionally substituted with halo, CN, oxo, C_-6 alkyl, d_6 alkoxy, (Cι-6 alkyl) carbonyl, 5 (d-6 alkyl) sulfonyl, mono- or dialkylamino, mono- or dialkylaminocarbonyl, mono- or dialkylaminocarbonyloxy, or 5-6 membered heteroaryl;
(b) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two
10 adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is a naphthyl ring, and R1 is -halo, a Cχ-4 aliphatic group optionally substituted with halogen, or -CN; or Ring D is an optionally substituted ring selected from phenyl, pyridinyl,
15 piperidinyl, piperazinyl, pyrrolidinyl, morpholinyl, 1,2,3, -tetrahydroisoquinolinyl, 1,2,3,4- tetrahydroquinolinyl, isoquinolinyl, quinolinyl, or naphthyl ;
(c) R2 is hydrogen or a Cι-6 aliphatic group; and 20 (d) each R5 is independently selected from -Cl,
-F, -CN, -CF3, -NH2, -NH(d-4 aliphatic), -N(d-4 aliphatic)2/ -0(d_ aliphatic), Cι_4 aliphatic, and -C02(Cι-4 aliphatic) , and when Ring G is Ring D, Ring D is substituted by oxo or R5. 25 Representative compounds of formula IX are shown below in Table 8.
Table - 8 .
IX- 1 IX- 2 IX- 3
IX-10 IX-11 IX- 12
IX-19 IX-20 IX-21
IX-22 IX-23 IX-24
IX-28 IX-29 IX- 3.0
-31 IX-32 IX-33
IX-40 IX-41 IX-42
IX-55 IX-56 IX-57
IX-58 IX- 59 IX-60
IX-61 IX-62 IX-63
IX- 64 ' IX-65 IX-66
IX-67 IX- 68 IX-69
IX- 70 IX-71 IX-72
IX-73 IX-74 IX-75
IX-79 IX-80 IX-81
•IX- 82 IX- 83 IX- 84
IX- 85 IX-86 IX-87
IX-88 IX- 89 IX-90
IX-91 IX-92 IX-93
-94 IX-95 -96
IX-97 IX-98 IX-99
-100 IX-101 IX-102
IX-103 IX-104 IX-105
IX-106 IX-107 IX-108
IX-112 IX-113 IX-114
IX-115 IX-116 IX-117
IX- 118 IX-119 IX- 120
I -124 IX-125 IX-126
-130 -131 -132
IX-133 IX-134 IX-135
IX-136 IX-137 IX-138
IX-139 IX-140 IX- 141
IX- 142 IX- 143 IX- 144
IX-145 IX- 146 IX-147
IX-148 IX-149 IX-150
IX-151 IX-152 IX-153
IX-154 IX-155 IX-156
IX-160 IX-161 IX-162
IX-172 IX-173 IX-174
In another embodiment, this invention provides a composition comprising a compound of formula IX and a pharmaceutically acceptable carrier.
One aspect of this invention relates to a method of inhibiting GSK-3 activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula IX.
7Λnother aspect relates to a method of treating a disease that is alleviated by treatment with a GSK-3 inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula IX.
7Another aspect relates to a method- of enhancing glycogen synthesis and/or lowering blood levels of glucose in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula IX. This method is especially useful for diabetic patients. 7Λnother aspect relates to a method of inhibiting the production of hyperphosphorylated Tau protein in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula IX. This method is especially useful in halting or slowing the progression of Alzheimer's disease. Another aspect relates to a method of inhibiting the phosphorylation of β-catenin in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of a composition comprising a compound of formula IX. This method is especially useful for treating schizophrenia.
One aspect of this invention relates to a method of inhibiting Aurora activity in a patient, comprising administering to the patient a therapeutically effective amount of a composition comprising a compound of formula IX.
Another aspect relates to a method of treating a disease that is alleviated by treatment with an Aurora inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of a composition comprising a compound of formula IX. This method is ' especially, useful for treating cancer, such as colon, ovarian, and breast cancer.
Another method relates to inhibiting GSK-3 or Aurora activity in a biological sample, which method comprises contacting the biological sample with the GSK-3 or Aurora inhibitor of formula IX, or a pharmaceutical composition thereof, in an amount effective to inhibit GSK-3 or Aurora.
Each of the aforementioned compositions and methods directed to the inhibition of GSK-3 or Aurora, or the treatment of a disease alleviated thereby, is preferably carried out with a preferred compound of formula IX, as described above. The compounds of this invention may be prepared as illustrated by the Synthetic Methods below, by the Synthetic Examples described herein and by general methods known to those skilled in the art.
General Synthetic Methods
The general synthetic methods below provide a series of general reaction routes that were used to prepare compounds of this invention. Methods A-F below are particularly useful for preparing formula II compounds. In most cases, Ring C is drawn as a phenyl ring bearing an ortho R1 substituent. However, it will be apparent to one skilled in the art that compounds having other Ring C groups may be obtained in a similar manner. Methods analogous to methods A-F are also useful for preparing other compounds of this invention. Methods F-I below are particulary useful for preparing compounds of formula III or IV.
Method A
II
Method A is a general route for the preparation of compounds wherein ring C is an aryl or heteroaryl ring. Preparation of the starting dichloropyrimidine 1 may be achieved in a manner similar to that described in Chem. Pharm. Bull . , 30, 9, 1982, 3121-3124. The chlorine in position 4 of intermediate 1 may be replaced by an aminopyrazole or aminoindazole to provide intermediate 2 in a manner similar to that described in J. Med. Chem. , 38, 3547-3557 (1995) . Ring C is then introduced using a boronic ester under palladium catalysis (see Tetrahedron, 48, 37, 1992, 8117-8126) . This method is illustrated by the following procedure.
A suspension of 1H-quinazoline-2, 4-dione (10.0 g, 61.7 mmol) in POCl3 (60 L, 644 mmol) and N,N- dimethylaniline (8mL, 63.1 mmol) is heated under reflux for 2 h. Excess POCl3 is evaporated under vacuum, the residue is poured into ice, and the precipitate is collected by filtration. The crude solid 2,4- dichloroquinazoline product may be used without further purificatio .
To a solution of 2,4-dichloro-quinazoline (3.3 g, 16.6 mmol) in anhydrous ethanol (150 mL) is added 5- methyl-lJϊ-pyrazol-3-yl amine (3.2 g, 32.9 mmol). The mixture is stirred at room temperature for 4 h, and the resulting precipitate is collected by filtration, washed with ethanol, and dried under vacuum to afford (2-chloro- quinazolin-4-yl) - (5-methyl-lff-pyrazol-3-yl) -amine.
To a solution of (2-chloro-quinazolin-4-yl) - (5- methyl-lH-pyrazol-3-yl) -amine (50 mg, 0.19 mmol) in DMF (1.0 mL) is added the desired arylboronic acid (0.38 mmol), 2M Na2C03 (0.96 mmol), and tri-t-butylphosphine (0.19 mmol). Under nitrogen, PdCl2 (dppf) (0.011 mmol) is added in one portion. The reaction mixture is then heated at 80°C for 5 to 10 hours, cooled to room temperature, and poured into water (2 mL) . The resulting precipitate is collected by filtration, washed with water, and purified by HPLC.
Method B (i)
(iii)
Methods B through F describe routes where the pyrazole ring system is introduced after Ring C and the . pyrimidine ring portion are first constructed. A versatile intermediate is the 4-chloropyrimidine 4, which is readily obtained from pyrimidinone 3 as shown in Method B(i). This reaction sequence is generally applicable for a variety of Ring C groups including aliphatic, aryl, heteroaryl, or heterocyclyl. See J. Med. Chem. , 38, 3547-3557 (1995).
For quinazoline ring systems (where Rx and Ry are taken together to form a benzo ring) , the useful intermediate 6 may be obtained by condensing an anthranilic acid or its derivative with a benzamidine as shown in Method B(ii) or by condensing a benzoylchloride with an anthranilamide as shown in Method B(iii) .' Many substituted anthranilic acid, anthranilamide, benzamidine and benzoylchloride starting materials may' be obtained by known methods. See Aust . J. Chem. , 38, 467-474 and J". Med. Chem. , 38, 3547-3557 (1995). Method B(iii) is illustrated by the following procedure.
To a solution of anthranilamide (33 mmol) in THF and CH2C12 (1:1, 70 mL) is added the desired benzoylchloride (33 mmol) , and triethylamine (99 mmol) at room temperature. The mixture is stirred for about 14 hours . The resulting precipitate is collected by filtration, washed with CH2C12 and water, and dried under vacuum. The crude 2-benzoylaminobenzamide may be used directly for the next step without further purification.
To a solution of the above crude product (13 mmol) in ethanol (50 mL) is added NaOEt (26 mmol) at room temperature. The mixture is heated under reflux for 48 to 96 h. The solvent is evaporated and the residue is neutralized using concentrated HC1 to pH 7. The product is then collected by filtration and dried under vacuum to provide 2-phenyl-3H-quinazolin-4-one that may be used without further purification. To a suspension of the above product (12 mmol) in POCl3 (120 mmol) is added tri-n-propylamine (24 mmol) . The mixture is heated under reflux for lh. After removal of the excess P0C13 by evaporation, the residue is dissolved in ethyl acetate, and washed with IN NaOH (twice) and water (twice) . The organic layer is dried over MgS04, the solvent is evaporated under vacuum, and the crude product is purified by flash chromatography (eluting with 10% of ethyl actetate in hexanes) to give 4-chloro-2-aryl quinazoline. To a solution of 4-chloro-2-aryl quinazoline
(0.16 mmol) in DMF (or THF, ethanol) (1 mL) is added the desired aminopyrazole or aminoindazole (0.32 mmol). The mixture is heated in DMF (or THF under reflux) at 100 to 110°C for 16 h (or in ethanol at l30-160°C for 16 hours) and then poured into water (2 mL) . The precipitate is collected by filtration and purified by HPLC.
Method C
Method D(i)
R'Λ CO_Et
_L
10 11
Methods C and D(i) above employ β-ketoesters 8 and 10, respectively, as pyrimidinone .precursors. The substitution pattern of the Rx and Ry groups on the pyrimidinone ring will be reversed if a chlorocrotonate 11 (Synth. Comm, (1986), 997-1002), instead of the corresponding β-ketoester 10, is condensed with the desired benzamidine. These methods are illustrated by the following general procedure.
To a solution of a β-ketoester (5.2' mmol) and amidinium chloride (5.7 mmol) in ethanol (5 mL) .is added sodium ethoxide (7.8 mmol) . The mixture is heated under reflux for 7-14 hours. After evaporation the resulting residue is dissolved in water, acidified with concentrated HC1 to pH 6, and then filtered to obtain a solid product 2-aryl-3H-pyrimidin-4-one (yield 75-87%) , which may be purified by flash column chromatography if needed. To this pyrimidinone (3.7 mmol) is added P0C13 (4 L) and n-Pr3N (1.4 L) . The mixture is heated under reflux for 1 hour. After evaporation of the excess P0C13, the residue is dissolved in ethyl acetate, washed with IN NaOH solution (three times) and NaHC03 (once) , and dried over MgS04. The solvent is removed under vacuum and the residue is purified by flash column chromatography eluting with 10% of ethyl acetate in hexanes to give 2- aryl-4-chloro-pyrimidine as a pale yellow syrup. This crude product may be treated with a 3-aminopyrazole or 3- aminoindazole as described above.
Method D ( ii)
Method D(ii) above shows a general route for the preparation of the present compounds, such as compound 40, wherein Rγ is N(R4)2. See 11 Farmaco, 52(1) 61-65 (1997) . Displacement of the 6-chloro group is exemplified here using morpholine. This method is illustrated by the following procedure.
To a solution of 2-methylmalonic acid diethyl ester (5 mmol) and sodium ethoxide (15 mmol) is added the appropriate amidine salt (5 mmol) in ethanol (10 mL) and the reaction heated at reflux for 2-24 hours. The residue is dissolved in water and acidified with 2N HCl. The resulting precipitate is filtered off and further purified by flash chromatography (yield 5-35%) to afford the pyrimidinedione 37. To 37 (1.6 mmol) is added P0C13 (32 mmol) and tri-n-propylamine (6.4 mmol) and the reaction refluxed is for lh. After evaporation of excess P0C13, the residue is dissolved in ethyl acetate, basified with IN NaOH, separated and the aqueous phase twice more extracted with ethyl acetate. The combined organics are dried (sodium sulfate) and evaporated. Purification by flash chromatography provides the dichloropyrimidine (38) as a yellow oil in 23% yield. A solution of 38 (0.33 mmol) in methanol (5 mL) is treated with an amine, exemplified here using morpholine (0.64 mmol) and refluxed 1 hour. After evaporation of solvent, the residue is purified by flash chromatography to provide the mono-chloropyrimidine 39 as a colorless oil in 75% yield.
The mono-chloropyrimidine, 39, (0.19 mmol) may be treated with a 3-aminopyrazole or 3-aminoindazole compound in a manner substantially similar those described above in Methods A and B.
Method E
9 (Rx = H)
As shown by Method E, an acyl isocyanate 12 may be condensed with an enamine to provide uvrimidinone 9 (J. Org. Chem (1993), 58, 414-418; J.Med. Chem., (1992), 35, 1515-1520; J. Org. Chem., 91967, 32, 313-214). This method is illustrated by the following general procedure. The enamine is prepared according to W. White, et al, J. Org Chem. (1967), 32, 213-214. The acyl isocyanate is prepared according to G Bradley, et al, J Med. Chem. (1992), 35, 1515-1520. The coupling reaction then follows the procedure of S Kawamura, et al, J. Org. Chem, (1993), 58, 414-418. To the enamine (10 mmol) in tetrahydrofuran (30 mL) at 0°C under nitrogen is added dropwise over 5 min a solution of acyl isocyanate (10 mmol) in tetrahydrofuran (5 mL) . After stirring for 0.5 h> acetic acid (30 mL) is added, followed by ammonium acetate (50 mmol) . The mixture is refluxed for 2 h with continuous removal of tetrahydrofuran. The reaction is cooled to room temperature and is poured into water (100 mL) . The precipitate is filtered, washed with water and ether and dried to provide the 2-aryl-3H-pyrimidin-4-one.
Method F
Method F shows a general route for the preparation of the present compounds wherein Rx and Rγ are taken together to form a 5-8 membered partially unsaturated saturated or unsaturated ring having 1-3 heteroatoms. The condensation of a 2-amino-carboxylic acid, such as 2-amino-nicotinic acid 13, and an acid chloride 7 provides an oxazinone 14. Treatment of 14 with ammonium hydroxide will furnish the benzamide 15 which may be cyclized to a 2- (substituted) -pyrido [2, 3- d] [l,3]pyrimidin-4-one 16. This method is illustrated by the following procedure.
2- (Trifluoromethyl) benzoyl chloride (4.2 ml, 29.2 mmol) is added dropwise to a solution of 2- aminonicotinic acid (2.04g, 14.76 mmol) in 20 ml of pyridine. The reaction mixture is. heated at 158 C for 30 min then cooled to room temperature. The reaction is poured into 200 ml of water and an oil forms which solidifies upon stirring. The solid is collected by vacuum filtration and washed with water and diethyl ether. The product is dried to give 2- (2- trifluoromethyl-phenyl) -pyrido [2, 3-d] [1,3] oxazin-4-one (2.56 g, 60% yield) which may be used in the next step without further purification.
2- (2-Trifluoromethyl-phenyl) -pyrido [2,3- d] [1, 3] oxazin-4-one (2.51g) is stirred in 30% ammonium hydroxide (25 ml) at room temperature overnight. The resulting precipitate is filtered and rinsed with water and diethyl ether. The precipitate is dried under vacuum at 50 C overnight to give 2- (2-trifluoromethyl- benzoylamino) -nicotinamide (850 mg, 33% yield)
2- (2-Trifluoromethyl-benzoylamino) -nicotinamide (800mg, 2.6mmol) is dissolved in 10ml of ethanol. Potassium ethoxide (435mg, 5.2mmol) is added to the solution which is heated to reflux for 16 h. The reaction mixture is evaporated in vacuo to afford a gummy residue that is dissolved i water and acidified with 10% sodium hydrogen sulfate to pH 7. The resulting precipitate is filtered and dried under vacuum at 50 C to give 2- (2-trifluoromethyl-phenyl) -3H-pyrido [2,3- d] pyrimidin-4-one . Method G
Method G is analogous to Method B(i) above. This method is illustrated by the following general procedure . 2- (3, 4-Dichloro-phenyl) -3H-quinazolin-4-one
(lg, 3.43 mmol) is suspended in phosphorus oxychloride (4 mL) and the reaction mixture was stirred at 110°C for 3 hours . The solvents are then evaporated and the residue is treated carefully with an .ice cold aqueous saturated solution of NaHC03. The solid is collected by filtration and washed with ether to give 4-chloro-2- (3 , 5-dichloro- phenyl) -quinazoline as a white solid (993 mg, 93%).
To 4-chloro-2- (3, 5-dichloro-phenyl) -quinazoline (4.00mg, 1.29 mmol) in THF (30 mL) is added 3-amino-5- methyl pyrazole (396 mg, 2.58 mmol) and the reaction mixture is heated at 65°C overnight. The solvents are then evaporated and the residue triturated with ethyl acetate, filtered and washed with a minimum amount of ethanol to give [2- (3, 4-dichlorophenyl) -quinazolin-4-yl] - (5-methyl-2H-pyrazol-3-yi) -amine as a white solid (311 mg 65%): mp 274°C; ^ NMR (DMSO) δ 2.34 (3H, s) , 6.69 (1H, s) , 7.60 (1H, m) , 7.84 (1H, d) , 7.96 (2H, d) , 8.39 (1H, dd) , 8.60 (1H, d) , 8.65 (1H, d) , 10.51 (1H, s) , 12.30 (1H, s) ; IR (solid) 1619, 1600, 1559, 1528, 1476, 1449, 1376, 1352, 797, 764, 738; MS 370.5 (M+H)+.
The THF solvent used, in the previous step may be replaced by other organic solvents such as ethanol, N,N-dimethylformamide, or dioxane.
Method H
( i) 17 18
( ii) 1 19
Method H shows routes in which a Ring D aryl group bearing a halogen (X is Br or I) may be converted to other formula III compounds. Method H(i) shows a phenylboronic acid coupling to Ring D to provide compound 18 and Method H(ii) shows an acetylene coupling to provide compound 19. Substituent X in compound 17 may be bromine or iodine. These methods are illustrated by the following procedures .
Method H(i) . To a mixture of [2- (4-bromo- phenyl) -quinazolin-4-yl] - (5-methyl-2H-pyrazol-3-yl) -amine (196 mg, 0.51 mmol) and phenylboronic acid (75 mg, 0.62 mmol) in THF/water (l/l, 4 L) is added Na2C03 (219 mg, 2.06 mmol), triphenylphosphine (9mg, 1/15 mol%) and palladium acetate (1 mg, 1/135 mol%) . The mixture is heated at 80°C overnight, the solvents are evaporated and the residue is purified by flash chromatography (gradient of CH2Cl2/MeOH) to give (2-biphenyl-4-yl-quinazolin-4-yl) - (5-methyl-2H-pyrazol-3-yl) -amine as a yellow solid (99 mg, 51%) :XH NMR (DMSO) δ 2.37 (3H, s) , 6.82 (1H, s) , 7.39- 7.57 (4H, m) , 7.73-7.87 (6H, m) , 8.57 (2H, d) , 8.67 (1H, d) , 10.42 (1H, s) , 12.27 (1H, s) ; MS 378.2 (M+H) +
Method H(ii) . To a mixture of [2-(4-bromo- phenyl) -quinazolin-4-yl] - (5-methyl-2Jf-pyrazol-3-yl) -amine (114 mg, 0.3 mmol), and trimethylsilylacetylene (147 mg, 1.5 mmol) in DMF (2 mL) is added Cul (1.1 mg, 1/50 mol%) , Pd(PPh3)2Cl2 (4.2 mg, 1/50 mol%) and triethylamine (121 mg, 0.36 mmol) . The mixture is heated at 120°C overnight and the solvent is evaporated. The residue is triturated in ethyl acetate and the precipitate is collected by filtration.
To the above precipitate suspended in THF (3 mL) is added tetrabutylammonium fluoride (IM in THF, 1. leq) . The reaction mixture is stirred at room temperature for two hours and the solvent is evaporated. The- residue is purified by flash chromatography (gradient of CH2Cl2/MeOH) to give [2- (4-ethynylphenyl) -quinazolin-4- yl] - (5-methyl-2H-pyrazol-3-yl) -amine as a white solid (68 mg, 70%): XH NMR (DMSO) δ 2.34 (3H, s)1, 4.36 (1H, s) , 6.74 (1H, s) , 7.55 (1H, m) , 7.65 (2H, d) , 7.84 (2H, m) , 8.47 (2H, d) , 8.65 (1H, d) , 10.43 (1H, s) , 12.24 (1H, s) ; MS 326.1 (M+H)+
Method I
Method I above shows a general route for the preparation of the present compounds wherein ring D is a heteroaryl or heterocyclyl ring directly attached to the pyrimidine 2-position via a nitrogen atom. Displacement of the 2-chloro group, exemplified here using piperidine, may be carried out in a manner similar to that described in J". Med. Chem. , 38, 2763-2773 (1995) and J. Chem. Soc , 1766-1771 (1948) . This method is illustrated by the following procedure.
To a solution of (2-chloro-quinazolin- -yl) -
(lH-indazol-3-yl) -amine (1 equivalent, 0.1-0.2 mmol) in N, N-dimethylacetamide (1 ml) is added the desired amine
(3 equivalents) . The resulting mixture is maintained at 100°C for 6 h and then purified by reverse-phase HPLC.
Method J
21 22
23 24
Method J above shows the preparation of compounds of formula V via the displacement of a chloro group from an appropriately substituted pyridyl ring. Method J(i) is a route for preparing compounds of formula Va (see Indian J. Chem. Sect . B, 35, 8., 1996, 871-873) - Method J(ii) is a "route for preparing compounds of formula Vb (see Bioorg. Med. Chem. , 6 , 12, 1998, 2449- 2458) . For convenience, the chloropyridines 21 and 23 are shown with a phenyl substituent corresponding to Ring D of formula V. It would be apparent to one skilled in the art that Method J is also useful for preparing compounds of formula V wherein Ring D is heteroaryl, heterocyclyl, carbocyclyl or other aryl rings. Method J is illustrated by the following procedures .
Method J(i) . (5-Methyl-2iϊ-pyrazol-3-yl) - (2 - phenyl-quinolin-4-yl) -amine. To 4-chloro-2- phenylquinoline (J. Het. Chem., 20, 1983, 121-128) (0.53g, 2.21 mmol) in diphenylether (5 mL) was added 3-amino-5- methylpyrazole (0.43g, 4.42 mmol) and the mixture was heated at 200°C overnight with stirring. To the cooled mixture was added petroleum ether (20 mL) and the resulting crude precipitate was filtered and further washed with petroleum ether. The crude solid was purified by flash chromatography (Si02, gradient DCM-MeOH) to give the title compound as a white solid: mp 242-244°C; XH NMR (DMSO) δ 2.27 (3H, s) , 6.02(1H, s) ,. 7.47(2H, d) , 7.53- 7.40(2H, br m) , 7.67(1H, m) , 7.92(1H, m) , 8.09(2H, d) , 8.48(2H, m) , 9.20(1H, s) , 12.17(1H, br s) ; IR (solid) 1584, 1559, 1554, 1483, 1447, 1430, 1389; MS 301.2 (M+H) + Method J(ii) . (5-Methyl-2H-pyrazol—3-yl) - (3- phenyl-isoquinolin-1-yl) -amine. To l-chloro-3- phenylisoquinoline (J. Het. Chem., 20, 1983, 121- 128) (0.33g, 1.37 mmol) in dry DMF (5 mL) was added 3- amino-5-methylpyrazole (0.27g, 2.74 mmol) and potassium carbonate (0.57g, 4.13 mmol) and the mixture was heated under reflux for 6 hours. The mixture was cooled and the bulk of DMF was evaporated. The residue was extracted twice with ethyl acetate and the combined organic layers were washed with brine, dried (MgS04) , filtered and concentrated. The crude was purified by flash chromatography (Si0 , gradient DCM-MeOH) to give the title compound as a colourless oil; 2H NMR (MeOD) δ 2.23 (3H, s) , 5.61 (1H, s) , 7.41 (1H, m) , 7.52(2H, m) , 7.62 (1H, m) , 7.81(1H, m) , 8.07(1H, d) , 8.19(2H, m) , 8.29(1H, s) , 8.54 (1H, d) ; MS 301.2 (M+H) +
Method K
2 27
Method K shows a route for the preparation of compounds of formula VI . A versatile starting material is 2,4, 6-trichloro- [1, 3, 5] triazine 25 in which the chlorine substituents may be sequentially displaced. The displacement of one of the chlorines by an aryl Grignard reagent or an aryl boronic acid is described in PCT patent application WO 01/25220 and Helv. Chim. Acta, 33, 1365 (1950) . The displacement of one of the chlorines by a heteroaryl' ring is described in WO 01/25220; J. Het . Chem. , 11, 417 (1974); and Tetrahedron 31, 1879 (1975). These reactions provide a 2, 4-dichloro- (6- substituted) [1, 3, 5] triazine 26 that is a useful intermediate for the preparation of compounds of formula VI. Alternatively, intermediate 26 may be obtained by constructing the triazine ring by known methods. See US patent 2,832,779; and US patent 2,691020 together with J. Am. Chem. Soc. 60, 1656 (1938) . In turn, one of the chlorines of 26 may be displaced as described above to provide 2-chloro- (4, 6-disubstituted) [1, 3 , 5] triazine 27. The treatment of 27 with an appropriate aminopyrazole provides the desired compound of formula VI .
Method L
31
Method L shows a route for preparing compounds of formula VII. For illustration purposes the trifluoromethylchalcone 28 is used as a starting material; however, it would be apparent to one skilled in the art that other rings may be used in place of the trifluoromethylphenyl and phenyl rings of compound 28. Substituted chalcones may be prepared by known methods, for example as described in the Indian J. Chemistry, 32B, 449 (1993) . Condensation of a chalcone with urea provides the pyrimidinone 29, which may be treated with P0C13 to give the chloropyrimidine 30. See J". chem. Eng. Data, 30(4) 512 (1985) and Egypt . J. Chem. , 37(3), 283 (1994) . In an alternative approach to compound 30, one of the aryl rings attached to the pyrimidine is introduced by displacement of of the 4-chloro group of 2, 4-dichloro- (6-aryl) -pyrimidine by an aryl boronic acid using a palladium catalyst such as (Ph3P)4Pd in the presence of a base such as sodium carbonate as described in Bioorg. Med. Lett . , 9(7), 1057 (1999). Displacement of the chlorine of compound 30 by an appropriate aminopyrazole provides compounds of this invention, such as 31. The last step of this method is illustrated by the following procedure.
[4- (4-Methylpiperidin-l-yl) -pyrimidin-2-yl] - (5- methyl-2H-pyrazol-3-yl) -amine. To a solution of 2- chloro-4- (4-methylpiperidin-l-yl) -pyrimidine (prepared using a procedure similar to the one reported in I?ur. J". Med. Chem. , 26(7) 729 (1991) ) (222 mg, 1.05 mmol) in BuOH (5 mL) was added 3-amino-5-methyl-2H-pyrazole (305mg,
3.15 mmol) and the reaction mixture was then heated under reflux overnight. The solvent was evaporated and the residue dissolved in a mixture ethanol/water (1/3, 4 mL) . Potassium carbonate (57mg, 0.41 mmol) was added and- the mixture was stirred at room temperature for 2 hours. The resulting suspension was filtered, washed with water twice and rinsed with ether twice to give the title . compound as a white solid (143mg, 50%) : mp 193-195°C; XH NMR (DMSO) δ 0.91 (3H, d) , 1.04 (2H, m) , 1.67 (3H, ) ,
2.16 (3H, s) , 2.83 (2H, t) , 4.31 (2H, m) , 6.19 (2H, m) , 7.87 (1H, d) , 8.80 (1H, br s) , 11.71 (1H, s) ; IR (solid) 1627, 1579, 1541, 1498, 1417, 1388, 1322., 1246; MS 273.3 (M+H)+.
Method M Villa
VII b
33
VIIIc
34
Vlϊld
35
Method M provides routes for obtaining compounds of formula VIII. A general procedure for displacing the chlorine of a 4-chloro-6-substituted- pyridazine, 32, with an appropriately substituted pyrazole to provide Villa is described in J". Het . Chem. , 20, 1473 (1983) . Analogous reactions may be carried out as follows: (a) with 3-chloro-5-substituted-pyridazine, 33, to provide Vlllb is described in J". Med. Chem. , 41(3), 311 (1998); (b) with 5-chloro-3-substituted- [1, 2, 4] triazine, 34, to provide VIIIc is described in Heterocycles , 26(12), 3259 (1987); and (c) with 3-chloro- 5-substituted- [1,2,4] triazine, 35, to provide Vllld is described in Pol . J. Chem. , 57, 7, (1983); Indian J. Chem. Sect . B, 26, 496 (1987); and Agric. Biol . Chem. , 54(12), 3367 (1990). An alternative procedure to compounds of formula VIIIc is described in Indian J. Chem. Sect . B, 29(5), 435 (1990).
Compounds of formula IX are prepared by methods substantially similar to those described above for the pyrazole-containing compounds of formula I. Methods A-J may be used to prepare the triazole-containing compounds' of formula IX by replacing the amino-pyrazole compound with an amino-triazole compound. Such methods are specifically exemplified by Synthetic Examples 415-422 set forth below. The amino-triazole intermediate may be obtained by methods described in <J. Org. Chem. USSR, 27, 952-957 (1991) .
Certain synthetic intermediates that are useful for preparing the protein kinase inhibitors of this invention are new. Accordingly, another aspect of this invention relates to a 3-aminoindazole compound of formula A:
A where R10 is one to three substituents that are each independently selected from fluoro, bro o, C-6 haloalkyl, nitro, or 1-pyrrolyl. Examples of such compounds include the following:
Al A2 A3 A4
A5 A6 A7 A8
A9 A10
Another aspect of this invention relates to a 4-chloropyrimidine compound of formula B:
B wherein Rx and Ry are as defined above; R1 is selected from Cl, F, CF3, CN, or N02; and is one to three substituents that are each independently selected from H, Cl, F, CF3, N02, or CN; provided that R1 and R5 are not simultaneously Cl . Examples of compounds of formula B are shown below:
Bl B2 B3
B7 B8 B9
BIO Bll B12
B13 B14 B15
B17 B18
B20 Another aspect of this invention relates to compounds of formula C:
wherein Rx, Ry, R2, and R2' are as defined above. Examples of compounds of formula C are shown below:
C2 C3
C4 C5 C6
C7 C8 C9 CIO Cll C12
C13 C14 CIS
Yet another aspect of this invention relates to compounds of formula D :
D
where R5 , R and Ry are as defined above . Examples of formula D compounds and other useful pyrimidinone intermediates are shown below:
DI D2 D3
D4 D5 D6
D7 D8 D9
D10 Dll D12
D14 D15
D16 D17 D18
In order that the invention described herein may be more fully understood, the following examples ■ are set forth. It should be understood that these examples are for illustrative purposes only and are not to be construed as limiting this invention in any manner. - SYNTHETIC EXAMPLES The following HPLC methods were used in the analysis of the compounds as specified in the Synthetic Examples set forth below. As used herein, the term "Rt" refers to the retention time observed for the compound using the HPLC method specified.
HPLC-Method A: Column: C18, 3 urn, 2.1 X 50 mm, "Lighting" by Jones Chromatography.
Gradient: 100% water (containing 1% acetonitrile, 0.1% TFA) to 100% acetonitrile (containing 0.1% TFA) over 4.0 min, hold at 100% acetonitrile for 1.4 min and return to initial conditions . Total run time 7.0 min. Flow rate: 0.8 mL/min.
HPLC-Method B:
Column: C18, 5 um, 4.6 X 150 mm "Dynamax" by Rainin Gradient: 100% water (containing 1% acetonitrile,
0.1% TFA) to 100% acetonitrile (containing 0.1% TFA) over 20 min, - hold at 100% acetonitrile for 7.0 min and return to initial conditions . Total run time 31.5 min. Flow rate: 1.0 mL/min.
HPLC-Method C:
Column: Cyario, 5 um, 4.6 X 150 mm "Microsorb" by
Varian.
Gradient: 99% water (0.1% TFA), 1% acetonitrile (containing 0.1% TFA) to 50% water (0.1% TFA) , 50% acetonitrile (containing 0.1% TFA) over 20 min, hold for 8.0 min and return to initial conditions . Total run- time 30 min. Flow rate: 1.0 mL/min. HPLC-Method D:
Column: Waters (YMC) ODS-AQ 2.0x50mm, S5, 120A. Gradient: 90% water (0.2% Formic acid), 10% acetonitrile (containing 0.1% Formic acid) to 10% water (0.1% formic acid), 90% acetonitrile (containing 0.1% formic acid) over 5.0 min, hold for 0.8 min and return to initial conditions . Total run time 7.0 min. Flow rate: 1.0 mL/min.
HPLC-Method E:
Column: 50x2.0mm Hypersil C18 BDS;5 μm Gradient: elution 100% water (0.1% TFA), to 5% water (0.1% TFA), 95% acetonitrile (containing 0.1% TFA) over 2.1 min, returning to initial conditions after 2.3 min. Flow rate: 1 mL/min.
Example 1 [2- (2-Clorophenyl) -5, 6-dimethylpyrimidin-4-yl] - (5-Methyl-2H-pyrazol-3-yl) -amine (II-l) : XHNMR (500 MHz, DMS0-d6) δlθ.4 (s, br, IH) , 7.74 (m, 2H) , 7.68 (m, IH) , 7.60 (m, IH) , 6.39 (s, IH) , 2.52 (s, 3H) , 2.30 (s, 3H) , 2.22 (S, 3H) ; ' MS 314.1 (M+H).
Example 2 [2- (2-Chloro-phenyl) -6, 7, 8, 9-tetrahydro-5ff- cycloheptapyrimidin-4-yl] - (lH-indazol-3-yl) -amine (II- 2) : Prepared in 30% yield. ^ΗNMR (500MHz, DMSO-d6) δ 1^72 (m, 4H) , 1.91 (m, 2H) , 3.02 (m, 4H) , 7.05 (t, IH) , 7.33 (t, IH) , 7.39 (m, IH) , 7.47 (d, IH) , 7.55 (m, 3H) , 7.59 (d, IH) , 10.4. ( , IH) , 13.11 (br. s, IH) ; EI-MS 390.2 (M+H) ; HPLC-Method A, Rt 2.99 min. Example 3 (5~Fluoro-lH-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -5,6,7, 8-tetrahydro-pyrido [3,4- d]pyrimidin-4-yl] -amine (II-3) : Compound 11-18 (90 mg, 0.17 mmol) was treated with an equal weight of Pd/C (10%) in 4.4% formic acid in MeOH at room temperature for 14 h. The mixture was filtered through celite, the filtrate was evaporated, and crude product was purified by HPLC to provide 18 mg (24%) of the desired product as pale yellow solid. XHNMR (500 MHz, DMSO-d6) δ 12.9 (s, IH) , 9.51 (s, IH) , 9.26 (s, 2H) , 7.72 (d, IH) , 7.63 (t, IH) , 7.58 (t,
IH) , 7.49 (m, 2H) , 7.21 (td, IH) , 7.15 (dd, IH) , 4.24 (s, - 2H) , 3.56 (m, 2H) , 2.95 (m, 2H) ppm. MS (ES+) : m/e= 429.22 (M+H); HPLC-Method A, Rt 2.88 min.
Example 4 [2- (2-Chloro-phenyl) -6, 7, 8, 9-tetrahydro-5ff- cycloheptapyrimidin-4-yl] - (7-fluoro-lH-indazol-3-yl) - amine (II-4) : Prepared in 52% yield to afford a white solid. ^NMR (500MHz, DMSO-d6) δ 1.72 (m, 4H) , 1.92 (m, 2H) , 3.00 ( , 4H) , 7.02 (td, IH) , 7.20 (dd, IH) , 7.40 (m, IH) , 7.42 (d, IH) , 7.52 (m, 3H) , 10.5 (m, IH) , 13.50 (br. s, IH) ; EI-MS 408.2 (M+H); HPLC-Method A, Rt 3.00 min.
Example 5 [2- (2-Chloro-phenyl) -6,7, 8, 9-tetrahydro-5H- cycloheptapyrimidin-4-yl] - (5-fluoro-lH-indazol-3-yl) - amine (II- 5) : Prepared in 51% yield. XHNMR (500MHz, DMSO- d6) δ 1.71 (m, 4H) , 1.91 (m, 2H.) , 3.01 (m, 4H) , 7.24 (td, IH) , 7.41 (m, 2H) , 7.54 ( , 4H) , 10.5 (m, IH) , 13.1 (br. s, IH) ; EI-MS 408.2 (M+H); HPLC-Method A, Rt 3.05 min.
' Example 6 [2- (2-Chloro-phenyl) -6, 7, 8, 9-tetrahydro-5H- cycloheptapyrimidin-4-yl] - (5, 7-difluoro-lH-indazol-3-yl) - amine (II-6) : Prepared according to Method C in 72% yield. 1HNMR (500MHz, DMS0-d6) δ 1.72 (m, 4H) , 1.91 (m, 2H) , 3.01 (m, 4H) , 7.'31 (m, 2H) , 7.41 (m, IH) , 7.54 (m, 3H) , 10.5 (m, IH) , 13.6 (br. s, IH) ; EI-MS 426.2 (M+H); HPLC-Method A, Rt 3.21 min.
Example 7 (7-Fluoro-lH-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -5,6,7, 8-tetrahydroquinazolin-4- yl] -amine (II-7) : Prepared in 62% yield. ^ΗNMR (500 MHz, DMSO-d6) δl3.5 (s, br, IH) , 10.1 (s,- br, IH) , 7.75 (m, 4H) , 7.33 (d, IH) , 7.17 (dd, IH) , 7.00 (td, IH) , 2.80 (m, 2H) , 2.71 (m, 2H) , 1.89 (br, 4H) ppm; LC-MS (ES+) 428.44 (M+H), (ES-) 426.43 (M-H) ; HPLC-Method A, Rt 3.02 min.
Example 8 (5-Fluoro-lH-indazol-3-yl) -. [2- (2- trifluoro ethyl-phenyl) -5, 6,7, 8-tetrahydroquinazolin-4~ yl] -amine (II-8) : Prepared in 53% yield. 1HNMR (500 MHz, DMSO-d6) δl3.1 (s, IH) , 10.2 (s, br, IH) , 7.75 (m, 4H) , 7.50 (dd, IH) , 7.27 (dd, IH) , 7.21 (td, IH) , 2.80 (m, 2H) , 2.72 (m, 2H) , 1.88 (m, 4H) ppm; MS (ES+) 428.43 (M+H), (ES-) 426.43 (M-H); HPLC-Method A, Rt 3.01 min.
Example 9 (5, 7-Difluoro-lff-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -5,6,7, 8-tetrahydroquinazolin-4- yl] -amine (II-9) : Prepared in 37% yield. 1HNMR (500 MHz, DMSO-d6) δl3.7 (s, IH) , 10.2 (s, br, IH) , 7.80 (d, IH) , 7.76 (t, IH) , 7.69 (m, 2H) , 7.31 (t, IH) , 7.18 (d, IH) , 2.81 (t, br, 2H) , 2.72 (t, br, 2H) , 1.90 (m, 4H) ppm; MS (ES+) 446.42 (M+H), (ES-) 444.37 (M-H); HPLC-Method A, Rt 3.09 min.
Example 10 (5-Trifluoromethyl-lH-indazol-3 -yl) - [2- (2- trifluoromethyl-phenyl) -5,6,7, 8-tetrahydroquinazolin-4- yl] -amine (11-10) : Prepared by Method C in ethanol in 35% yield. ^ΗNMR (500 MHz, DMSO-d6) δl3.2 (s, IH) , 10.1 (s, br, IH) , 8.01 (s, IH) , 7.76 (d, IH) , 7.66 (m, 4H) , 7.57 (d, IH) , 2.79 (m, 2H) , 2.73 (m, 2H) , 1.89 (m, 4H) ppm. MS (ES+) 478.45 (M+H), (ES-) 476.42 (M-H); HPLC- Method A, R 3.21 min. '
Example 11 (5,7-difluoro-lff-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -6,7,8, 9-tetrahydro -5H- cycloheptapyrimidin-4-yl] -amine (11-11) : Prepared in 60% yield. White solid. XHNMR (500MHz, DMSO-d6) δ 1.72 (m, ' 4H) , 1.91 (m, 2H) , 3.01 (m, 4H) , 7.15 (dd, IH) , 7.30 (td, IH) , 7.66 (m, 2H) , 7.72 (t, IH) , 7.78 (d, IH) , 10.2 (m, IH) , 13.5 (br. s, IH) ; EI-MS 460.2 (M+H); HPLC-Method A, Rt 3.13 min. .
Example 12 (6-Benzyl-2- (2-trifluoromethyl-phenyl) - 5,6,7, 8-tetrahydro-pyrido [4, 3-d]pyrimidin-4-yl) - (5- fluoro-lH-indazol-3-yl) -amine (11-12) : Prepared in 49% yield. XHNMR (500 MHz, DMSO-d6) δ 12.8 (s, IH) , 9.11 (s., ' IH) , 7.68 (d, IH) , 7.58 (t, IH) , 7.53 (t, IH) , 7.44 (m, 4H) , 7.37 (t, 2H) , 7.29 (t, IH) , 7.19 (m, 2H) , 3.78 (s, 2H) , 3.61 (s, 2H) , 2.81 (s, br, 4H) ppm; LC-MS (ES+) 519.24 (M+H); HPLC-Method A, Rt 3.11 min.
Example 13 (lH-Indazol-3-yl) - [2- (2-trifluoromethyl- phenyl) -6, 7, 8, 9-tetrahydro-5iϊ-cycloheptapyrimidin- -yl] - amine (11-13) :_Prepared in 40% yield. ^NMR (500MHz, DMSO-d6) δ 1.70 (m, 4H) , 1.90 (m, 2H) , 3.00 (m, 4H) , 7.01 (t, IH) , 7.30 (td, IH) , 7.44 (d, IH) , 7.49 (d, IH) , 7.68 (m, 3H) , 7.77 (d, IH) , 10.01 (m, IH) , 12.83 (s, IH) ; EI- MS 424.2 (M+H); HPLC-Method A, Rt 3.17 min.
Example 14 (7-Fluoro-UT-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -6,7, 8, 9-tetrahydro-5H- cycloheptapyrimidin-4-yl] -amine (11-14) : Prepared in 78% yield. HNMR (500MHz, DMS0-d6) δ 1.71 (m, 4H) , 1.91 (m, 2H) , 3.00 (m, 4H) , 6.98 (td, IH) , 7.16 (dd, IH) , 7.31 (d, IH) , 7.68 (m, 3H) , 7.77 (d, IH) , 10.25 (m, IH) , 13.40 (br. s, IH) ; EI-MS 442.2 (M+H); HPLC-Method A, Rt 3.12 min.
Example 15 (5-Fluoro-lH-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -6,7,8, 9-tetrahydro- 5H- cycloheptapyrimidin-4-yl] -amine (11-15) : Prepared in 63% yield. XHNMR (500MHz, DMS0-d6) δ 1.71 (m, 4H) , 1.91 (m, 2H) , 3.00 (m, 4H) , 7.20 (td, IH) , 7.25 (dd, IH) , 7.49 (dd, IH) , 7.69 (br. t, 2H) , 7.74 (m, IH) , 7.79 (d, IH) , 10.35 (m, IH) , 13.00 (br. S, IH) ; EI-MS 442.2 (M+H); HPLC-Method A, Rt 3.21 min.
Example 16 (5-Fluoro-lH-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -5,6,7, 8-tetrahydro-pyrido [4,3- d]pyrimidin-4-yl] -amine (11-16): A solution of compound 11-12 (45mg, 0.087 mmol) in methanol (4.4% HCOOH) was treated with an equal weight of Pd/C (10%) at room temperature for 14 h. The mixture was filtered through celite, the filtrate evaporated, and the crude product was purified by preparative HPLC to provide 15 mg (41%) of the desired product as yellow solid. XHNMR (500 MHz, DMSO-d6) δl2.9 (s, IH) , 9.52 (s, IH) , 9.32 (s, 2H, TFA- OH) , 7.72 (d, IH) , 7.59 ( , 2H) , 7.49 ( , 2H) , 7.21 (m, IH) , 7.15 (m, IH) , 4.31 (s, 2H) , 3.55 (s, 2H) , 3.00 (m, 2H) ppm; LC-MS (ES+) 429.20 (M+H); HPLC-Method A, Rt 2.79 min.
Example 17 (lH-indazol-3 -yl) - [2 - (2 -trif luoromethyl - phenyl) -5, 6 , 7 , 8 -tetrahydroquinazolin-4 -yl] -amine (11-17) : Prepared in 58% yield. 1HNMR (500 MHz, DMSO-d6) δ 13.0 (s, IH) , 10.3 (s, br, IH) , 7.74 (m, 4H) , 7.51 (d, IH) , 7.47 (d, IH) , 7.32 (t, IH) , 7.03 (t, IH) , 2.82 (m, 2H) , 2.73 (m, 2H) , 1.90 (m, 4H) ppm; LC-MS (ES+) 410.21 (M+H); HPLC-Method A, Rt 2.99 min.
Example 18 (7-Benzyl-2- (2-trifluoromethyl-phenyl) - 5,6,7, 8-tetrahydro-pyrido [4, 3-d]pyrimidin-4-yl) - (5- fluoro-lH-indazol-3-yl) -amine (11-18) : Prepared from compound Bll in 92% yield. 1HNMR (500 MHz, DMSO-d6) δl2.9 (s, IH) , 10.5 (s, br, IH) , 9.58 (s, IH, TFA-OH) , 7.71 (d, IH) , 7.52 (m, 9H) , 7.19 (m, 2H) , 4.57 (s, 2H) , 4.20 (m, 2H) , 3.70 (m, 2H) , 3.00 (m, 2H) ppm; LC-MS (ES+) 519.23 (M+H); HPLC-Method A, Rt 3.23 min.
Example 19 (lff-Indazol-3-yl) - [6-methyl-2- (2- trifluoromethyl-phenyl) -pyrimidin-4-yl] -amine (11-19) : Prepared in 42% yield. Melting point 235-237°C; ^NMR (500 MHz, DMSO) δ 2.44 (3H, s) , 7.09 (IH, J=7.5 Hz, t) , 7.40 (IH, J=7.1 Hz, t) , 7.49 (IH, J=8.3 Hz, d) , 7.70 (3H, m) , 7.79 (IH, J=7.3 Hz, t) , 7.87 (IH, J=8.3 Hz, d) , 8.03 (IH, J=7.7 Hz, d) , 10.3 (IH, s) , 12.6 (IH, s) ppm; HPLC- Method A, Rt 2.958 min; MS (FIA) 370.2 (M+H)+.
Example 20 (lH-Indazol-3-yl) - [6-phenyl-2- (2- trif luoromethyl -phenyl) -pyrimidin-4-yl] -amine (11-20) :
Prepared in 32% yield. ^ΗNMR (500 MHz, DMSO) δ 6.94 (IH, J=7.4 Hz, t), 7.24 (IH, J=7.4 Hz, t) , 7.33 (IH, J=8.4 Hz, d) , 7.42 (3H, m) , 7.57 (IH, J=7.3 Hz, t) , 7.68 (2H, m) , 7.75 (IH, J=7.9 Hz, d) , 7.93 (3H, m) , 8.18 (IH, br s) ,
10.45 (IH, br s) , 12.5 (IH, br s) ppm; HPLC-Method A, Rt 4.0 min; MS (FIA) 432.2 (M+H)+. Example 21 (lH-Indazol-3-yl) - [6- (pyridin-4-yl) -2- (2- trifluoromethyl-phenyl) -pyrimidin-4-yl] -amine (11-21) : Prepared in 12% yield. ^Η MR (500 MHz, DMSO) δ 7.16 (IH, J=7.4 Hz, t), 7.46 (IH, J=7.6 Hz, t) , 7.56 (IH, J=8.3 Hz, d) , 7.80 (IH, J=7.2 Hz, t) , 7.90 (2H, m) , 7.97 (IH, J=7.8 Hz, d) , 8.09 (IH, br) , 8.22 (2H, J= .9 Hz, d) , 8.45 (IH, br s) , 8.93 (2H, J=4.8 Hz, d) , 10.9 (IH, br s) , 12.8 (IH, br s) ppm; HPLC-Method A, Rt 3.307 min; MS (FIA) 433.2 (M+H) +
Example 22 (lH-Indazol-3-yl) - [6- (pyridin-2-yl) -2- (2- trifluoromethyl-phenyl) -pyrimidin-4-yl] -amine (11-22) : Prepared in 42% yield. XHNMR (500 MHz, DMSO) δ 7.07 (IH, J=7.4 Hz, t), 7.36 (IH, J=7.4 Hz, t) , 7.46 (IH, J=7.4 Hz, d) , 7.53 (IH, J=5.0 Hz, t) , 7.70 (IH, J=7.4 Hz, t) , 7.79 (IH, J=7.1 Hz, t) , 7.83 (IH, J=7.4 Hz, d) , 7.88 (IH, J=7.8 Hz, d) , 7.97 (IH, J=7.7 Hz, t) , 8.02 (IH, J=5.5 Hz, br d) , 8.36 (IH, J=7.8 Hz, d) , 8.75 (2H, J=4.1 Hz, d) , 10.5 (IH, br s) , 12.7 (IH, br s) ppm; HPLC-Method A, Rt 3.677 min; MS (FIA) 433.2 (M+H)+.
Example 23 [6- (2-Chlorophenyl) -2- (2-trifluoromethyl- phenyl) -pyrimidin-4-yl] - (lH-indazol-3-yl) -amine (11-23) :
Prepared in 44% yield; 1HNMR (500 MHz, DMSO) δ 7.08 (IH, J=7.5 Hz, t) , 7.37 (IH, J=7.5 Hz, t) , 7.45 (IH, J=8.4 Hz, d) , 7.51 (2H, m) , 7.61 (IH, J=7.4, 1.9 Hz, dd) , 7.69 (2H, m) , 7.79 (2H, J=4.0 Hz, d) , 7.86 (3H, J=7.8 Hz, d) , 8.04 (2H, J=6.2 Hz, br d) , 10.7 (IH, br s) , 12.6 (IH, br s) ppm; HPLC-Method A, Rt 3.552 min; MS (FIA).466.2 (M+H)+.
Example 24 [5, 6-Dimethyl-2- (2-trifluoromethyl-phenyl) - pyrimidin-4-yl] - (lH-indazol-3-yl) -amine (11-24): Prepared in 35% vield; mo 183-186°C: ^ΗNMR (500 MHz. DMSO) δ 2.14 ( 3H, s) , 2 . 27 ( 3H, s) , 6 . 85 ( IH , J=7 . 5 Hz , t) , 7 . 15 ( IH, J=7 . 6 Hz , t ) , 7 . 32 ( 3H, m) , 7 . 38 ( IH, J=7 . 5 Hz , t) , 7 . 42
(IH, J=7.4 Hz, t) , 7.53 (IH, J=7.6 Hz, d) , 8.88 (IH, s) , 12.5 (IH, s) ppm; HPLC-Method A, Rt 2.889 min.; MS (FIA) 384.2 (M+H)'.
Example 25 [5, 6-Dimethyl-2- (2-trifluoromethyl-phenyl) - pyrimidin-4-yl] - (5-fluoro-lH-indazol-3-yl) -amine (11-25) :
Prepared in 44% yield. Melting point 160-163°C; 1HNMR (500 MHz, DMSO) δ 2.27 (3H, s) , 2.40 (3H, s) , 7.16 (2H, m) , 7.44 (2H, m) , 7.52 (IH, J=7.4 Hz, t) , 7.57 (IH, J=7.4 Hz, t) , 7.67 (IH, J=7.8 Hz, d) , 9.03 (IH, s) , 12.75 (IH, s) ppm; HPLC-Method A, Rt 2.790 min; MS (FIA) 402.2 (M+H)+.
Example 26 [2- (2-Chlorophenyl) -5, 6-dimethyl-pyrimidin-4- yl] - (lff-indazol-3-yl) -amine (11-26): Prepared in 30% yield. 1HNMR (500 MHz, DMSO) δ 2.14 (3H, s) , 2.33 (3H, s) , 6.84 (IH, J=7.4 Hz, t) , 7.13 (IH, J=7 ,4 Hz, t) , 7.19 (IH, J=6.9 Hz, br t), 7.27 (IH, J=7.4 Hz, d) , 7.32 (3H, br m) , 7.37 (IH, J=7.1 Hz, d) , 10.0 (IH, br) , 12.8 (IH, br s) ppm; δ 2.919 min; MS (FIA) 350.1 (M+H)+.
Example 27 [5, 6-Dimethyl-2- (2-trifluoromethyl-phenyl) - pyrimidin-4-yl] - (7-fluoro-lff-indazol-3-yl) -amine (11-27):
Prepared in 92% yield. ^ΗNMR (500 MHz, DMSO) δ 2.33 (3H, s) , 2.50 (3H, s) , 6.97 (IH, m) , 7.15 (IH, m) , 7.30 (IH, J=8.1 Hz, d) , 7.65 (3H, m) , 7.76 (IH, J=7.5 Hz, d) , 10.0 (IH, s) , 13.4 (IH, s) ppm; HPLC-Method A, Rt 3.053 min; MS (FIA) 402.2 (M+H)+.
Example 28 (5,7-Difluoro-lH-indazol-3-yl) - [5, 6-Dimethyl- 2- (2-trifluoromethyl-phenyl) -pyrimidin-4-yl] -amine (II- 28).: Prepared in 50% yield. XHNMR (500 MHz, DMSO) δ 2.42 (3H, s) , 2.63 (3H, s) , 7.22 (IH, J=7.6 Hz, d) , 7.38 (IH, J=9.3, 1.7 Hz, dt) , 7.71 (IH, m) , 7.75 (IH, J=7.0 Hz, d) , 7.79 (IH, J=6.7 Hz, d) , 7.86 (IH, J=8.0 Hz, d) , 10.0. (IH, s) , 13.2 (IH, s) ppm; HPLC-Method" A, R 3.111 min; MS (FIA) 420.2 (M+H)+..
Example 29 [2- (2-Chloropheny1) -5, 6-dimethyl-pyrimidin-4- yl] - (5,7-difluoro-lH-indazol-3-yl) -amine (11-29) : Prepared in 58% yield. 1HNMR (500 MHz, DMSO) δ 2.47 (3H, S) , 2.66 (3H, s) , 7.44 (2H, m) , 7.53 (IH, m) , 7.64 (3H, m) , 10.4 (IH, br) , 13.8 (IH, br s) ppm; HPLC-Method A, Rt 2.921 min; MS (FIA) 386.1 (M+H)+.
Example 30 [2- (2-Chloropheny1) -5, 6-dimethyl-pyrimidin-4- yl] - (7-fluoro-lff-indazol-3-yl) -amine (11-30): Prepared in 70% yield. 1HNMR (500 MHz, DMSO) δ 2.35 (3H, s) , 2.51 (3H, s) , 7.03 (IH, J=7.8, 4.4 Hz, dt) , 7-22 (IH, m) , 7.33 (IH, J=7.4 Hz, t) , 7.42 (IH, m) , 9.19 (IH, s) , 13.3 (IH, s) ppm; HPLC-Method A, Rt 2.859 min; MS (FIA) 368.2 . (M+H)+.
Example 31 [2- (2-Chloropheny1) -5, 6-dimethyl-pyrimidin- - yl] - (5-fluoro-lH-indazol-3-yl) -amine (11-31): Prepared in 86% yield. 1HNMR (500 MHz, DMSO) δ 2.49 (3H, s) , 2.68
(3H, s) , 7.38 (IH, J=9.0 Hz, t) , 7.54 (2H, m) , 7.67 (4H, m) , 10.5 (IH, br) , 13.2 (IH, br s) ppm; HPLC-Method A, Rt 2.850 min; MS (FIA) 368.1 (M+H)+.
Example 32 [2- (2, 4-Dichlorophenyl) -5, e-dimethyl- pyrimidin^-yl] - (lff-indazol-3-yl) -amine (11-32): Prepared in 52% yield. XHNMR (500 MHz, DMSO) δ 2.46 (3H, s) , 2.64 (3H, s) , 7.16 (IH, J=7.5 Hz, t) , 7.46 (IH, J=7.6 Hz, t) ,
7.61 (2H, m) , 7.68 (2H, J=8.2 Hz, d) , 7.82 (IH, m) , 10.2 (IH, br) , 13.0 (IH, br s) ppm; HPLC-Method A, Rt 2.983. min; MS (FIA) 384.1 (M+H) .
Example 33 (5-Methyl-2ff-pyrazol-3-yl) - [2- (2- methylphenyl) -quinazolin-4-yl] -amine (11-33) : 1HNMR (DMSO) δ 1.21 (3H,s) , 2.25 (3H, s) , 6.53 (IH, s) , 7.38 (4H, m) ,
7.62 (IH, d) , 7.73 (IH, d) , 7.81 (IH, d) , 7.89 (IH, t) , 8.70 (IH, s) , 12.20 (IH, s) ; MS 316.3 (M+H)+.
Example 34 [2- (2,4-Dif luorophenyl) -quinazolin-4-yl] - (5- methyl-2H-pyrazol-3-yl) -amine (11-34) : 1HNMR (500 MHz, DMSO-d6) δl2.4 (br s, IH) , 10.8 (br s, IH) , 8.58 (d, IH) , 7.97 (m, IH) , 8.36 (m, IH) , 7.85 (m, IH) , 7.60 (m, IH) , 6.62 (s, IH) , 2.30 (s, 3H) ; MS 338.07 (M+H) .
Example 35 [2- (2, 5-Dimethoxyphenyl) -quinazolin-4-yl] - (5- methyl-2H-pyrazol-3-yl) -amine (11-35) : ^Η MR (500 MHz, DMSO-d6) δl2.5 (br s, IH) , 8.68 (br, IH) , 7.92 (t, J = 7.5 Hz, IH) , 7.86 (d, J = 8.2, Hz, IH) , 7.65 (t, J = 7.5 Hz, IH) , 7.45 (s, IH) , 7.14 (m, 2H) , 6.51 (s, IH) , 3.79 (s, 3H) , 3.67 (s,' 3H), 2.14 (s, 3H) ; MS 362.2 (M+H) .
Example 36 [2- (2 -Chloropheny 1) -quinazolin-4-yl] - (5- methyl-2H-pyrazol-3-yl) -amine (11-36) : XHNMR (500 MHz, DMSO-d6) δll.8 (br, IH) , 8.80 (d, J = 8.3 Hz, IH) , 8.00 (t, J = 7.6 Hz, IH) , 7.82 (d, J = 8.3 Hz, IH) , 7.78 (m, 2H) , 7.67 (d, J = 7.8 Hz, IH) , 7.61 (t, J = 7.0 Hz, IH) , 7.55 (t, J = 7.4 Hz, IH) , 6.56 (s, IH) , 2.18 (s, 3H) ; MS 336.1 (M+H) . Example 37 [2- (2-Methoxyphenyl) -quinazolin-4-yl] - (5- methyl-2H-pyrazol-3-yl) -amine (11-37): XHNMR (500 MHz, DMSO-d6) δ8.78 (s, br, IH) , 8.00 (t, J = 7.4 Hz, IH) , 7.90 (m, 2H) , 7.74 (t, J = 7.5 Hz, IH) , 7.63 (t, J = 7.3 Hz, IH) , 7.30 (d, J = 8.4 Hz, IH) , 7.18 (t, J = 7.5 Hz, IH) , 6.58 (s, br, IH) , 3.90 (s. 3H) , 2.21 (s, 3H) ; MS 332.1 (M+H) .
Example 38 [2- (2, 6-Dimethylphenyl) -quinazolin-4-yl] - (5- methyl-2#-pyrazol-3-yl) -amine (11-38): 1HNMR (500 MHz, DMSO-d6) δl2.2 (s, br, 2H) , 8.88 (d, J = 7.7 Hz, IH) , 8.05 (t, J = 7.7 Hz, IH) , 7.80 (m, 2H) , 7.37 (t, J = 7.6 HZ, IH) , 7.21 (d, J = 7.7 Hz, 2H) , 6.36 (s, IH) , 2.16 (s, 3H) , 2.15 (s, 6H) ; MS 330.1 (M+H).
Example 39 [2- (2-Acetylphenyl) -quinazolin-4-yl] - (5- methyl-2H-pyrazol-3-yl) -amine (11-39): XHNMR (500 MHz, DMSO-d6) δ 12.35 (s, br, IH) , 8.93 (d, J = 8.4 Hz, IH) , 8.37 (d, J = 8.6 Hz, IH) , 8.20 (d, J = 7.6 Hz, IH) , 8.11 (t, J = 8.0 Hz, 2H) , 7.89 (m, 2H) , 7.77 (m, 2H) , 6.93 (s, IH) , 2.33 (s, 3H) , 2.04 (s, 3H) MS 344.1 (M+H).
Example 40' [2- (2, 3-Dimethylphenyl) -quinazolin-4-yl] - (5- methyl-2ff-pyrazol-3-γl) -amine (11-40): ^NMR (500 MHz, DMSO-d6) δ 12.6 (s, br, IH) , 12.1 (s, br, IH) , 8.91 (d, J = 7.7 Hz, IH) , 8.14 (t, J = 7.2 Hz, IH) , 7.95 (d, J = 8.4 Hz, IH) , 7.89 (t, J = 7.7 Hz, IH) , 7.58 (d, J = 7.6 Hz, IH) , 7.53 (d, J = 7.0 Hz,' IH) , 7.42 (t, J = 7.6 Hz, IH) , 6 . 60 (s, IH), 2.43 (s, 3H) , 2.35 (s, 3H) , 2.32 (s, 3H) ; MS 330.1 (M+H) .
Example 41 (5-Methyl-2H-pyrazo1-3-yl) - [2- (2- trifluoromethylphenyl) -quinazolin-4-yl] -amine (11-41) : 1HNMR (500 MHz, DMSO-d6) δl2.3 (s, IH) , 10.5 (s, IH) , 8.77 (d, J = 8.2 Hz, IH) , 7.92 (m, 2H) , 7.85 (m, 3H) , 7.56 (t, J = 8.1 Hz, IH) , 7.67 (t, J = 7.4 Hz , IH) , 6.63 (s, IH) , 2.27 (s, 3H) ; MS 370.1 (M+H) .
Example 42 [2- (2-Ethylphenyl) -quinazolin-4-yl] - (5-Methyl- 2H-pyrazol-3-yl) -amine (11-42): ^ΗNMR (500 MHz, DMSO-d6) δ8.80 (m, IH) , 8.02 (s, br, IH) , 7.82' (d, J = 8.4 Hz, IH) , 7.77 (m, IH) , 7.62 (d, J = 7.6 Hz, IH) , 7.54 (m, IH) , 7.41 (m, 2H) , 6.40 (s, IH) , 2.75 (q, J = 7.1 Hz, 2H) , 2.17 (s, 3H) , 0.99 (t, J = 7.5 Hz, 3H) ; MS 330.1 (M+H) .
Example 43 (2-Biphenyl-2-yl-quinazolin-4-yl) - (5 -methyl - 2ff-pyrazol-3-yl) -amine (11-43) : XHNMR (500 MHz, DMSO-d6) δ 8.76 (d, J = 7.6 Hz, IH) , 8.04 (m, IH) , 7.75 (m, 6H) , 7.30 (m, 5H) , 5.34 (s, IH) , 2.14 (s, 3H) ; MS 378.2 (M+H) .
Example 44 [2- (2-Hydroxyphenyl) -quinazolin-4-yl] - (5- Methyl -2ff-pyrazol-3-yl) -amine (11-44) : ^NMR (500 MHz, DMSO-d6) δlθ.9 (s, br, IH) , 8.62 (d, J = 8.2 Hz, IH) , 8.28 (d, J = 7.9 Hz, IH) , 7.87 (m, 2H) , 7.60 (t, J = 7.9 Hz, IH) , 7.37 (t, J = 7.8 Hz, IH) , 6.92 (m, 2H) , 6.45 (s, IH) , 2.27 (s, 3H) ; MS 318.1 (M+H) .
Example 45 [2- (2-Ethoxyphenyl) -quinazolin-4-yl] - (5- Methyl-2ff-pyrazol-3-yl) -amine (11-45) : XHNMR (500 MHz, DMSO-d6) δl2.1 (s, br, IH) , 8.75 (d, J = 8.3 Hz, IH) , 7.97 (t, J = 7.8 Hz, IH) , 7.82 (d, J = 8.3 Hz, IH) , 7.78 (d, J = 7.5 Hz, IH) , 7.70 (t, J = 7.8 Hz, IH) , 7.56 (t, J = 7.8 Hz, IH) , 7.22 (d, J = 8.4 Ηz , IH) , 7.12 (t, J = 7.6 Hz, IH) , 6.55 (s, IH) , 4.11 (q, J = 6.9 Hz, 2H) , 2.16 (s, 3H) , 1.22 (t, J = 6.9 Hz, 3H) ; MS 346.1 (M+H) . Example 46 [5- (Thiophen-2-yl) -2ff-pyrazol-3-yl] - [2- (2- trifluoromethylphenyl) -quinazolin.-4-yl] -amine (11-46) :
1HNMR,(500 MHz, DMSO-d6) δ 8.04 (d, J = 8.3 Hz, IH) , 8.05 (dd, J = 7.3, 8.2 Hz, IH) , 7.93 (d, J = 6.5 Hz, IH) , 7.81 (m, 5H) , 7.34 (d, J = 5.0 Hz, IH) , 7.25 (m, IH) , 7.00 (m, IH) , 6.87 (s, IH) ; MS 438.1 (M+H).
Example 47 [4- (Thiophen-2-yl) -2H-pyrazol-3-yl] - [2- (2- trifluoromethylphenyl) -quinazolin-4-yl] -amine (11-47):
Prepared according to Method B. XHNMR (500MHz, DMSO-d6) δ 6.97 (m, IH) , 7.08 (m, IH) , 7.27 (m, IH) , 7.36 (m, IH) , 7.66 (m, 2H) , 7.77 (m, 3H) , 7.83 (m, IH) , 8.00 (m, IH) , 8.18 (s, IH) , 8.62 (d, J = 8.2 Hz, IH) , 10.7 (br. s, IH) ; EI-MS 438.1 (M+H); HPLC-Method A, Rt 2.97 min.
Example 48 (4-Phenyl-2ff-pyrazol-3-yl) - [2- (2- trifluoromethylphenyl) -quinazolin-4-yl] -amine (11-48) :
Prepared according to Method B. ^NMR (500MHz, DMSO-d6) δ 7.05 (br. s, IH) , 7.14 (t, J = 7.8 Hz, IH) , 7.25 (m, 3H) , 7.43 (m, 2H) , 7.60 (m, 2H) , 7.73 (m, 2H) , 7.80 (d, IH) , 7.95 (m, IH) , 8.12 (br. s, IH) , 8.60 (m, IH) , 10.6 (br. s, IH) ; EI-MS 432.2 (M+H); HPLC-Method A, Rt 3.04 min.
Example 49 (5-tert-Butyl-2H-pyrazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-49) :
XHNMR (500 MHz, DMSO-d6) δ 8.76 (d, J = 8.3 Hz, IH) , 7.94 (m, 2H) , 7.79 (m, 4H) , 7.70 (t, J = 7.6 Hz, IH) , 6.51 (s, IH) , 1.16 (s, 9H) ; MS 412.2 (M+H).
Example 50 (5-Phenyl-2H-pyrazol-3-yl) - [2- (2- trifluoromethylphenyl) -quinazolin-4-yl] -amine (11-50) :
XHNMR (500MHz, DMS0-d6) δ 7.09 (s, IH) , 7.36 (td, J = 7.8, 1.1 Hz, IH) , 7.46 (t, J = 7.8 Hz, 2H) , 7.65 (br. d, J = 8.1 Hz, 2H) , 7.78 (m, 2H) , 7.90 (m, 4H) , 7.95 (d, J = 7.7 Hz, IH) , 8.00 (t, J = 7.8 Hz, IH) , 8.81 (d, J = 8.6 Hz, IH) , 11.29 (br. s, IH) ; EI-MS 432.1 (M+H); HPLC-Method A, Rt 3.24 min.
Example 51 (4, 5-Diphenyi-2H-pyrazol-3-yl) - [2- (2- trifluoromethylphenyl) -quinazolin-4-yl] -amine (11-51) :
^ΗNMR (500MHZ, DMSO-d6) δ 7.13 ( , IH) , 7.18 (m, 5H) , 7.36 (m, 5H) , 7.62 (m, 3H) , 7.73 (m, 2H) , 7.85 (m, IH) , 8.48 (d, J = 8.7 Hz, IH) , 10.02 (s, IH) , 13.19 (s, IH) ; EI-MS 508.2 (M+H); HPLC-Method A, Rt 3.39 min.
Example 52 (4-Carbamoyl-2H-pyrazol-3-yl) - [2- (2- trifluoromethylphenyl) -quinazolin-4-yl] -amine (11-52) :
Prepared in 40% yield. ^ΗNMR (500MHz, DMSO-d6) : δ 12.85 (s, IH) , 12.77 (s, IH) , 11.80 (s, IH) , 10.80 (s, IH) , 8.35-7.42 (m, 9H) ; MS 399.13 (M+H) HPLC-Method'A, Rt 2.782 min.
Example 53 (2H-Pyrazol-3-yl) - [2- (2- trifluoromethylphenyl) -quinazoliή-4-yl] -amine (11-53) : Prepared in 38% yield. 1HNMR (500 MHz, DMSO-d6) δ 12.52 (s, IH) , 10.65 (s, IH) , 8.75 (d, . IH) , 7.91-7.68 (m, 8H) , 6.87 (s, IH) . MS: (M+H) 356.17. HPLC-Method A, Rt 2.798 min.
Example 54 (5-Hydroxy-2ff-pyrazol-3-yl) - [2- (2- trif luoromethylphenyl) -quinazolin-4-yl] -amine (11-54) : Prepared in 36% yield; XHNMR (500 MHz , DMSO-d6) δ 10 . 61 ( s , IH) , 8 . 75 ( s , IH) , 8 . 03 -7 . 75 (m, 9H) , 5 . 97 ( s , IH) ; MS 372 . 18 (M+H) ; HPLC-Method A, Rt 2 . 766 min . Example 55 (5-Cyclopropyl-2H-pyrazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-55) :
Prepared in 30% yield. XHNMR (500 MHz, DMSO-d6) δ 12.21 (s, IH) , 10.45 (s, IH) , 8.68 (s, IH) , 7.89-7.45 (m, 8H) , 6.48 (s, IH) , 0.89 (m, 2H) , 0.62 (s, 2H) . MS 396.18 (M+H); HPLC-Method A, Rt 3.069 min.
Example 56 (5-Methoxymethyl-2ff-pyrazol-3-yl) - [2- (2- trxfluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-56) : Prepared in 33% yield; XHNMR (500 MHz, DMSO-d6) δ 12.51
(s, IH), 10.48 (s, IH) , 8.60 (s, IH) , 7.81-7.55 (m, 7H) , 6.71 (s, IH) , 4.28 (s, 2H) , 3.18 (s, 3H) . MS 400.19 (M+H): HPLC-Method A, Rt 2.881 min.
Example 57 (lH-indazol-3-yl) - [2- (2-trifluoromethylphenyl) -quinazolin-4-yl] -amine (11-57) : Prepared to afford 51 mg (78% yield) as pale yellow solid. XHNMR (500 MHz, DMSO-d6) δ 12.7 (s, IH) , 10.4 (s, IH) , 8.55 (d, IH) , 7.81 (t, IH) , 7.71 (d, IH) , 7.61 (d, IH) , 7.58 (t, IH) , 7.46 (m, 4H) , 7.36 (d, IH) , 7.22 (t, IH) , 6.91 (t, IH) ppm; LC-MS (ES+) 406.16 (M+H), (ES-) 404.19 (M-H); HPLC- Method A, Rt 3.00 min.
Example 58 (4-Chloro-lff-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-58):
Prepared in DMF (70% yield) as pale yellow solid. XHNMR (500 MHz, DMS0-d6) δ 13.3 (s, br, IH) , 10.9 (s, br, IH) , 8.60 (d, IH) , 7.97 (t, IH) , 7.81 (d, IH) , 7.75 (t, IH) , 7.67 (d, IH) , 7.63 (dd, IH) , 7.57 (m, 2H) , 7.43 (d, IH) , 7.28 (dd, IH) , 7.08 (d, IH) ppm; LC-MS (ES+) 440.10
(M+H), (ES-) 438.12 (M-H); HPLC-Method A, Rt 3.08 min. Example 59 ( 5 -Fluoro- lff- indazol - 3 -yl) - [2 - (2 - trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-59) :
Prepared in DMF (34% yield) as pale yellow solid. XHNMR (500 MHz, DMSO-d6) δ 13.0 (s, IH) , 10.6 (s, IH) , 8.72 (d, IH) , 7.99 (t, 1H), 7.89 (d, IH) , 7.79 (d, IH) , 7.75 (t, IH) , 7.68 (m, 3H) , 7.56 (dd, IH) , 7.39 (d, IH) , 7.28 (t, IH) ppm; LC-MS (ES+) 424.12 (M+H), (ES-) m/e= 422.13 (M- H) ; HPLC-Method A, Rt 3.05 min.
Example 60 (7-Fluoro-lH-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-60) :
Prepared in DMF (51% yield) as yellow solid. XHNMR (500 MHz, DMSO-d6) δl3.4 (s, IH) , 10.6 (s, IH) , 8.68 (d, IH) , 7.95 (t, IH) , 7.85 (d,-lH), 7.72 (m, 2H) , 7.63 ( , 2H) , 7.58 (m, IH) , 7.43 (d, IH) , 7.18 (dd, IH) , 7.00 (m, IH) ppm; LC-MS (ES+) 424.11 (M+H), (ES-) 422.15 (M-H); HPLC- Method A, Rt 3.06 min.
Example 61 (5-Methyl-lff-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-61):
Prepared in DMF (81% yield) as yellow solid. XHNMR (500 MHz, DMSO-d6) δ 13.0 (s, br, IH) , 8.79 (br, IH) , 8.11 (br, IH) , 7.96 (d, IH) , 7.82 (m, 5H) , 7.46 (s, IH) , 7.41 (d, IH) , 7.20 (d, IH) , 2.33 (s, 3H) ppm; MS (ES+) 420.15 (M+H), (ES-) 418.17 (M-H); HPLC-Method A, Rt 3.07 min.
Example 62 [2- (2, 6-Dichloro-phenyl) -quinazolin-4-yl] - (5- fluoro-lff-indazol-3-yl) -amine (11-62): Prepared in DMF ' (37% yield) as yellow solid. XHNMR (500 MHz, DMSO-d6) δl3.0 (s, IH) , 10.8 (s, IH) , 8.72 (d, IH) , 7.97 (t, IH) , 7.90 (d, IH) , 7.75 (t, IH) , 7.53 (m, 3H) , 7.43 (t, IH) , 7.35 (d, IH) , 7.23 (t, IH) ppm; LCMS (ES+) 424.08 (M+H), (ES-) 422.10 (M-H); HPLC-Method A, Rt 3.06 min. Example 63 [2- (2-Chloro-phenyl) -quinazolin-4-yl] - (1H- indazol-3-yl) -amine (11-63): Prepared in 91% yield. XHNMR (500MHz, DMSO-d6) δ 7.06 (t, IH) , 7.36 (t, IH) , 7.39 (t, IH) , 7.52 (m, 3H) , 7.62 (d, IH) , 7.72 (d, IH) , 7.82 (m, IH) , 7.90 (d, IH) , 8.05 (m, IH) , 8.76 (d, IH) , 11.5 (m, IH) , 13.02 (s, IH) ; EI-MS 372.1 (M+l) ; HPLC-Method A, Rt 2.93 min.
Example 64 (5-Trifluoromethyl-Iff-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-64) :
Prepared in DMF (57% yield) as yellow solid. XHNMR (500 MHz, DMSO-d6) δl3.4 (s, br, IH) , 11.4 (br, IH) , 8.72 (d, IH) , 8.12 (s, IH) , 7.98 (t, IH) , 7.83 (d, IH) , 7.76 (d, IH) , 7.73 (dd, IH) , 7.60 (m, 4H) , 7.52 (d, IH) ppm; LC-MS (ES+) 474.12 (M+H), (ES-) 472.17 (M-H); HPLC-Method A, Rt 3.25 min.
Example 65 (4-Trifluoromethyl-Iff-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-65):
Prepared in DMF (8% yield) as yellow solid. XHNMR (500 MHz, DMSO-d6) δl3.7 (s, br, IH) , 11.2 (br, IH) , 8.70 (d, IH) , 8.05 (s,. IH) , 7.85 (m, 3H) , 7.65 (m, 4H) , 7.51 (m, 2H) ppm; LC-MS (ES+) 474.13 (M+H), (ES-) 472.17 (M-H); HPLC-Method A-, Rt 3.15 min.
Example 66 [2- (2, 6-Dichloro-phenyl) -quinazolin-4-yl] - (lff- indazol-3-yl) -amine (11-66): Prepared in DMF (30% yield) as yellow solid. XHNMR (500 MHz, DMS0-d6) δ 12.9 (s, IH) , 11.1 (s, IH) , 8.69 (d, IH) , 7.95 (t, IH)., 7.82 (d, IH) , 7.73 (t, IH) , 7.56 (d, IH) , 7.47 (s, IH) , 7.45 (s, IH) , 7.39 (m, 2H) , 7.26 (t, IH) , 6.92 (t, IH) ppm; LC-MS (ES+) 406.11 (M+H), (ES-) 404.12 (M-H); HPLC-Method A, Rt 3.00 min.
Example 67 (lff-indazol-3-yl) - [2- (2-methyl-phenyl) - quinazolin-4-yl] -amine (11-67): Prepared in 55% yield.
XHNMR (500MHz, DMS0-d6) δ 2.15 (s, 3H) , 7.09 (t, IH) , 7.26 (d, IH) , 7.31 (t, IH) , 7.39 (t, IH) , 7.42 (m, IH) , 7.55 (d IH) , 7.64 (d, IH) , 7.74 (d, IH) , 7.89 (m, IH) , 7.96 (d, IH) , 8.10 (m, IH) , 8.81 (d, IH) , 12.0 (m, IH) , 13.18 (s, IH) ; EI-MS 352.2 (M+l) ; HPLC-Method A, Rt 2.93 min.
Example 68 (7-Trifluoromethyl-Iff-indazol-3 -yl) - [2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-68) :
Prepared. in DMF (75% yield) as yellow solid. XHNMR (500 MHz, DMSO-d6) δ 13.5 (s, br, IH) , 11.2 ("s, br, IH) , 8.68 (d, IH) , 7.97 (t, IH), 7.92 (d, IH) , 7.82 (d, IH) , 7.74 (t, IH) , 7.70 (d, IH) , 7.68 (d, IH) , 7.64 (m, 2H) , 7.57 (m, IH) , 7.14 (t, IH) ppm; LC-MS (ES+) 474.11 (M+H), (ES-) 472.14 (M-H); HPLC-Method A, Rt 3.24 min.
Example 69 (6-Trifluoromethyl-Iff-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-69) : Prepared by Method B in DMF (78% yield) as yellow solid. XHNMR (500 MHz, DMSO-d6) δ 13.4 (s, br, IH) , 11.1 (s, br, IH) , 8.67 (d, IH) , 7.95 (t, IH) , 7.82 (m, 3H) , 7.72 (m, 2H) , 7.63 (m, 2H) , 7.57 (t, IH), 7.23 (d, IH) ppm; LC-MS (ES+) 474.12 (M+H), (ES-) 472.15 (M-H); HPLC-Method A, Rt 3.28 min.
Example 70 (5-Nitro-lff-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-70) :
Prepared in DMF (82% yield) as yellow solid. XHNMR (500 MHz, DMSO-d6) δ 13.6 (s, br, IH) , 11.4 (s, br, IH) , 8.75 (s, IH) , 8.72 (d, IH) , 8.09 (dd, IH) , 7.98 (t, IH) , 7.83 (d, IH) , 7.75 (t, IH) , 7.70 (m, 2H) , 7.61 (m, 3H) ppm; • LC-MS (ES+) 451.14 (M+H), (ES-) 449.12 (M-H); HPLC-Method A, Rt 3.02 min.
Example 71 (5,7-Difluoro-Iff-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-71) : Prepared in DMF (60% yield) as yellow solid. XHNMR (500 MHz, DMS0-d6) δl3.7 (s, br,. IH) , 11.2 (s, br, IH) , 8.73 (d, IH) , 8.03 (t, IH) , 7.88 (d, IH) , 7.80 (m, 2H) , 7.70
(m, 3H) , 7.32 (m, 2H) ppm; LC-MS (ES+) 442.14 (M+H), (ES- ) 440.14 (M-H); HPLC-Method A, Rt 3.11 min.
Example 72 (4-Pyrrol-1-yl-Iff-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-72):
Prepared in DMF (33% yield) as yellow solid. XHNMR (500
MHz, DMSO-d6) δl3.4 (s, br, IH) , 11.0 (s, br, IH) , 8.53
(d, IH) , 7.98 (t, IH) , 7.75 (m, 4H) , 7.62 (m, 2H) , 7.52
(d, IH) , 7.43 (t, IH) , 7.05 (d, IH) , 6.80 (s, 2H) , 5.61 (s, 2H) ppm; LC-MS (ES+) 471.18 ' (M+H) , (ES-) 469.18 (M-
H) ; HPLC-Method A, Rt 3.12 min.
Example 73 (5-Amino-lff-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-73): A solution of compound 11-70 (70 mg, 0.16 mmol) in MeOH (2 mL) was treated with Raney Ni until solution was colorless (about 1.5 g Raney Ni was added) . After stirring at room temperature for 40 min, the mixture was filtered through celite, the resulting celite was washed with MeOH (5 times) , and the solvent was evaporated in vacuo to provide a crude product that was then purified by HPLC to give the title compound as a yellow solid (10 mg, 15%) . m.p. 221-223°C; XHNMR (500 MHz, DMSO-d6) δl3.2 (s, br, IH) , 10.7 (s, br, IH) , 9.80 (br, 2H) , 8.68 (d, IH) , 7.97 (t, IH) , 7.87 (d, IH) , 7.75 (m, 2H) , 7.65 (m, 5H) , 7.30 (d, IH) ppm; MS (ES+) 421.16 (M+H) , (ES-) 419.17 (M-H) ; HPLC-Method A, Rt 2.41 min.
Example 74 [2- (2-Chloro-phenyl) -quinazolin-4-yl] - (7- fluoro-lff-indazol-3-yl) -amine (11-74) : Prepared in DMF (35% yield) as yellow solid. XHNMR (500 MHz, DMSO-d6) δl3.7 (s, IH) , 11.7 (s, br, IH) , 8.80 (d, IH) , 8.15 (t, IH) , 7.99 (d, IH) , 7.88 (t, IH) , 7.68 (d, IH) , 7.60 ( , 2H) , 7.53 (t, IH) , 7.46 (t, IH) , 7.25 (dd, IH) , 7.04 (m, IH) ppm; LC-MS (ES+) 390.16 (M+H) ; HPLC-Method A, Rt 3.00 min.
Example 75 [2- (2-Chloro-phenyl) -quinazolin-4-yl] - (5 - fluoro -Iff- indazol- 3 -yl) -amine (11-75) : Prepared in DMF. XHNMR (500 MHz, DMSO-d6) δ 13.2 (s, IH) , 11.7 (s, br, IH) , 8.80 (d, . IH) , 8.10 (t, IH) , 7.91 (m, 2H) , 7.70 (d, IH) , 7.58 (m, 4H) , 7.50 (t, IH) , 7.29 (t, IH) ppm; LC-MS (ES+) 390.17 (M+H) ; HPLC-Method A, Rt 3.00 min.
Example 76 [2- (2-Chloro-phenyl) -quinazolin-4-yl] - (5,7- di fluoro -Iff- indazol- 3 -yl) -amine (11-76) : Prepared in DMF (55% yield) as yellow solid. XHNMR (500 MHz, DMS0-d6) δl3.8 (s, IH) , 11.5 (s, br, IH) , 8.76 (d, IH) , 8.08 (t, IH) , 7.93 (d, IH) , 7.84 (t, IH) , 7.64 (d, IH) , 7.55 (d, IH) , 7.50 (t, IH) , 7.44 (m, 2H) , 7.36 (t, IH) ppm; LC-MS (ES+) 408.15 (M+H) , (ES-) 406.17 (M-H) ; HPLC-Method A, Rt 3.08 min.
Example 77 [2- (2-Chloro-phenyl) -quinazolin-4-yl] - (5- trifluoromethyl-Iff-indazol-3-yl) -amine (11-77): Prepared in DMF (66% yield) as yellow solid. XHNMR (500 MHz, DMSO- ά.6 ) δl3.5 (s, IH) , 11.4 (s, br, IH) , 8.79 (d, IH) , 8.29 (s, IH) , 8.07 (t, IH) , 7.93 (d, IH) , 7.84 (t, IH) , 7.72- (d, IH) , 7.63 (d, 2H) , 7.53 (d, IH) , 7.48 (t, IH) , 7.36 (t, IH) ppm; LC-MS (ES+) : m/e= 440.16 (M+H); (ES-): m/e= 438.18 (M-H); HPLC-Method A, Rt 3.22 min.
Example 78 [2- (2-cyano-phenyl) -quinazolin-4-yl] - (lff- indazol-3-yl) -amine (11-78): Prepared in 13% yield. XH- NMR (500 MHz, DMSO) δ 12.9 (br, IH) , 10.8 (br, IH) , 8.73 (br s, IH) , 7.97 (m, 4H) , 7.74 (m, IH) , 7.5 (m, 4H) , 7.42 (m, IH) , 7.08 (m, IH) ppm; MS (FIA) 363.2 (M+H); HPLC- Method A, Rt 2.971 min.
Example 79 (5-Bromo-lff-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-79) :
Prepared in DMF (64% yield) as yellow solid. XHNMR (500 MHz, DMSO-d6) δl3.4 (s, IH) , 11.6 (s, br, IH) , 8.93 (d, IH) , 8.21 (t, IH) , 8.14 (s, IH) , 8.05 (d, IH) , 7.95 (m, 4H) , 7.86 (t, IH) , 7.65 (d, IH) , 7.59 (d, IH) ppm; MS (ES+) 486.10 (M+H), (ES-) 484.09 (M-H); HPLC-Method A, Rt 3.22 min.
Example 80 (6-Chloro-lff-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-80) : Prepared in DMF (94% yield) as yellow solid. XHNMR (500 MHz, DMSO-d6) δl3.1 (s, IH) , 11.2 (s, br, IH) , 8.73 (d, IH) , 8.03 (t, IH) , 7.87 (d, IH) , 7.79 (m, 2H) , 7.73 (m, 2H) , 7.67 ( , 2H) , 7.58 (s,. IH) , 7.04 (dd, IH) ppm. LC-MS (ES+) 440.14 (M+H), (ES-) 438.16 (M-H); HPLC-Method A, Rt 3.25 min.
Example 81 (7-Fluoro-6-trifluoromethyl-Iff-indazol-3-yl) - 12 - (2-trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (II- 81) : Prepared in DMF (30% yield) as yellow solid. XHNMR (500 MHz, DMSO-d6) δ 13.9 (s, 1H), '11.0 (s, br, IH) , 8.64 (d, IH) , 7.94 (t, IH) , 7.81 (d, IH) , 7.71 (m, 2H) , 7.60 (m, 4H) , 7.20 (dd, IH) ppm. LC-MS (ES+) 492.18 (M+H), (ES-) 490.18 (M-H); HPLC-Method A, Rt 3.44 min.
Example 82 (6-Bromo-lff-indazol-3-vl) - [2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-82) :
Prepared in DMF (40% yield) as yellow solid. XHNMR (500 MHz, DMSO-d6) δ 13.1 (s, IH) , 11.2 (s, br, IH) , 8.73 (d, IH) , 8.03 (t, IH) , 7.87 (d, IH) , 7.80 (m, 2H) , 7.73 (m, 3H) , 7.67 (m, IH) , 7.61 (d, IH) , 7.15 (dd, IH) ppm; MS (ES+) 486.07 (M+H); HPLC-Method A, Rt 3.28 min.
Example 83 [2- (2, 4-Bis-trifluoromethyl-phenyl) - quinazolin-4-yl] - (5, 7 -difluoro-Iff-indazol-3 -yl) -amine (11-83) : Prepared in DMF in 28% yield. XHNMR (500MHz, MeOH-d4) δ 8.81 (d, J=8.4Hz, IH) , '8.35-8.20 (m, 3H) , 8.19-7.96 (m, 3H) , 7.40-7.34 (m, IH) , 7.29-7.14 (m, IH) ; LC-MS (ES+) 510.14 (M+H); HPLC-Method C, Rt 8.29 min.
Example 84 (5,7-Difluoro-Iff-indazol-3 -yl) - [2- (4-fluoro-2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-84) :
Prepared in 48% yield. XHNMR (500MHz, MeOH-d4) δ8.74- 8.63 (m, IH) , 8.23-8.10 (m, IH) , 7.99-7.90 (m, 2H) •, 7.89- 7.80 (m, IH) , 7.71-7.61 ( , IH) , 7.61-7.50 (m, IH) , 7.24- ' 7.15 "(m, IH) , 7.14-7.02 (m, IH) ; LC-MS (ES+) 460.14 (M+H); HPLC-Method C, Rt 7.59 min.
Example 85 [2- (2-Bromo-phenyl) -quinazolin-4-yl] - (5,7- difluoro-Iff-indazol-3 -yl) -amine (11-85): Prepared in THF (21% yield) . XHNMR (500MHz, MeOH-d4) δ8.81 (d, J=8.4Hz, IH) , 8.35-8.20 (m, 3H) , 8.19-7.96 (m, 3H) , 7.40-7.34 (m, IH) , 7.29-7.14 (m, IH) ; LC-MS (ES+) 510.14 (M+H); HPLC- Method C, Rt 8.29 min.
Example 86 (5, 7-Difluoro-Iff-indazol-3-yl) - [2- (5-fluoro-2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-86):
Prepared in THF (26% yield) . XHNMR (500MHz, MeOH-d4) δ8.62 (d, J=8.4Hz, IH) , 8.16-8.02 (m, IH) , 7.96-7.73 (m, 3H) , 7.59-7.48 (m, IH) , 7.48-7.35 (m, IH) , 7.21-7.09 (m, IH) , 7.09-6.89 (m, IH) ; LC-MS (ES+) 460.16 (M+H); HPLC- Method C, Rt 7.28 min.
Example 87 [2- (2,4-Dichloro-phenyl) -quinazolin-4-yl] - (5, 7-Difluoro-Iff-indazol-3-yl) -amine (11-87): Prepared in
THF (16% yield). XHNMR (500MHz, MeOH-d4) δ8.81 (d, J=8.4Hz, IH) , 8.35-8.20 (m, 3H) , 8.19-7.96 (m, 3H) , 7.40- 7.34 (m, IH) , 7.29-7.14 (m, IH) ; LC-MS (ES+) 510.14 (M+H); HPLC-Method C, Rt 8.29 min.
Example 88 [2- (2-Chloro-5-trifluoromethyl-phenyl) - quinazolin-4-yl] - (5, 7-Difluoro-Iff-indazol-3 -yl) -amine (11-88) : Prepared in THF (33% yield) . XHNMR (500MHz, DMSO-d6) δ 10.76 (s, IH) , 8.66 (d, J=8.3Hz, IH) , 8.06- 7.84 (m, 3H) , 7.81-7.63 (m, 3H) , 7.48-7.16 (m, 2H) ; LC-MS (ES+) 476.16 (M+H); HPLC-Method C, Rt 19.28 min.
Example 89 (4-Fluoro-Iff-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-89) : Prepared in NMP (79% yield) as yellow solid. XHNMR (500 MHz, DMSO-d6) δl3.2 (s, IH) , 10.8 (s, br, IH) , 8.63 (d, IH) , 7.97 (t, IH) , 7.85 (d, IH) , 7.74 (m, 2H) , 7.64 (t, IH) , 7.57 (m, 2H),.7.32 (m, 2H) , 6.82 (m, IH) ppm; LC-MS (ES+) 424.17 (M+H); HPLC-Method A, Rt 3.14 min. Example 90 (Iff-Indazol-3-yl) - [8-methoxy-2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-90) :
Prepared using THF as solvent to afford the title compound as a TFA salt (23% yield) . HPLC-Method A, Rt 2.97 min (95%); XHNMR (DMSO-d6, 500 MHz) δ 12.9 (IH, bs) , 11.0 - 10.7(1H, bs) , 8.2.5 (IH, m) , 7.75-7.50 (8H, s) , 7.30 (IH, ) ,• 6.90 (IH, m) , 4.0 (3H, s) ; MS (m/z) 436.2 (M+H).
Example 91 (5-Fluoro-Iff-indazol-3-yl) - [8-methoxy-2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-91):
Prepared using TFA as solvent to afford the title compound as a TFA salt (23% yield) . HPLC-Method A, Rt 3.10 min. (99%); XHNMR (DMSO-d6, 500 MHz): 13.0 (IH, bs) , 11.0 - 10.7(1H, bs) , 8.25 (IH, m) , 7.75-7.50 (7H, m) , 7.35 (IH, m) , 7.25 (IH, m) , 4.0 (3H, s) ; MS (m/z) 454.2 (M+H) .
Example 92 (7 -Fluoro-lff-indazol-3-yl) - [8-methoxy-2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-92) : Prepared using THF as solvent to afford the title compound as a TFA salt (98 mg, 58% yield) . HPLC-Method A, Rt 3.20 min (92%); XHNMR ' (DMSO-d6, 500 MHz) δ 13.45 (IH, bs) , 11.0 - 10.7(1H, bs) , 8.25 (IH, m) , 7.75-7.60 (5H, m) , 7.50 (IH, m), 7.40 (IH, m) , 7.15 (IH, m) , 6.95 (IH, m) 4.0 (3H, s) ; MS (m/z) 454.2' (M+H).
Example 93 (5, 7-Difluoro-Iff-indazol-3-yl) - [8-methoxy-2- (2-trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (II- •93) : Pre'pared using THF as solvent to afford the title compound as a TFA salt (36% yield) . HPLC-Method A, Rt
3.27 min. (95%); XHNMR (DMSO-d6, 500 MHz): 13.65 (IH, bs) , 11.0 - 10.7 (IH, bs) , 8.22 (IH, m) , 7.75-7.60 (5H, m) , 7 . 40 ( IH, m) , 7 . 35 ( IH, m) , 7 . 19 ( IH, m) , 4 . 0 (3H, s ) ; MS (m/z) 472 . 2 (M+H) .
Example 94 [2- (2-Chloro-pyridin-3-yl) -quinazolin-4-yl] - (5, 7-Difluoro-Iff-indazol-3-yl) -amine (11-94): Prepared in DMF. XHNMR (500MHz, DMSO-d6) δ 13.62 (br s, IH, 11.06- 10.71 (m, IH) , 8.16-7.70 (m, 4H) , 7.60-7.09 (m, 3H) ; LC- MS (ES+) 409.14 (M+H); HPLC-Method A, Rt 2.89 min.
Example 95 [2- (2-Chloro-4-nitro-phenyl) -quinazolin-4-yl] - (5, 7-difluoro-Iff-indazol-3-yl) -amine (11-95): Prepared in THF. XHNMR (500MHz, DMSO-d6) δ 13.35 (s, IH) , 10.74 (s, IH) , 8.67 (d, J=8.4Hz, IH) , 8.29 (d, J=2.05Hz, IH) , 8.18- 8.08 (m, IH) , 8.07-7.60 (m, 4H) , 7.53-7.10 (m, 2H) . LC- MS (ES+) 453.15 (M+H); HPLC-Method D, Rt 3.63 min.
Example 96 [2- (4-Amino-2-chloro-phenyl) -quinazolin-4-yl] - (5, 7-Difluoro-Iff-indazol-3-yl) -amine (11-96) :
A solution of compound 11-95 (8mg, 0.018mmol) and tin chloride dihydrate (22mg, O.lmmol) in ethanol (2mL) was heated at 100°C for 24h. The reaction was diluted with EtOAc (lOmL) , washed with IN NaOH solution (2xl0mL) , brine, and dried over anhydrous sodium sulfate to afford the crude product. Purification was achieved by flash chromatography on silica gel (eluting with 1-3% MeOH in CH2C12. ) The title compound was isolated as pale yellow solid (1.2mg, 16% yield) . LC-MS (ES+) 423.12 (M+H), HPLC-Method C, Rt 13.78 min.
Example 97 (4, 5, 6,7-Tetrahydro-lff-indazol-3-yl)
- [2 - (2 -trifluoromethyl-phenyl) -quinazolin-4-yl] -amine
(11 - 97 ) : Prepared in 34% yield . XHNMR ( 500MHz , DMSO-d6 ) δ 1 . 58 (m, 2H) , 1 . 66 (m, 2H) , 2 . 24 (m, 2H) , 2 . 54 (m 2H) , 7.63 (m, 3H) , 7.71 (t, IH) , 7.75. (d, IH) , 7.78 (d, IH) , 7.85 (t, IH) , 8.53 (d, IH) , 9.99 (s, IH) , 12.09 (s, IH) ; EI-MS 410.2 (M+l) ; HPLC-Method A, Rt 3.05 min.
Example 98 (lff-Pyrazolo [4, 3-b] yridin-3-yl) - [2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-98) :
Prepared in DMF (37% yield) as yellow solid. XHNMR (500 MHz, DMSO-d6) δl3.1.(s, br, IH) , 11.2 (s, br, IH) , 8.73
(d, IH) , 8.54 (dd, IH) , 8.12 (d, IH) , 8.06 (t, IH) , 7.90 (d, IH) , 7.84 (t, IH) , 7.75 (d, IH) , 7.69 (m, 2H) , 7.65
(t, IH) , 7.47 (dd, IH) ppm; LC-MS (ES+) 407.18 (M+H); HPLC-Method A, Rt 2.77 min.
Example 99 (lff-Pyrazolo [3, 4-b] pyridin-3-yl) - [2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-99):
Prepared in DMF (45% yield) . XHNMR (500 MHz, DMSO-d6) δl3.5 (s, br, IH) , 11.3 (s, br, IH) , 8.78 (d, IH) , 8.49 (d, IH) , 8.17 (d, IH) , 8.03 (t, IH) , 7.89 (d, IH) , 7.80 (m, 2H) , 7.74 ( , 2H) , 7.68 (m, IH) , 7.08 (dd, IH) ppm. MS '(ES+) 407.16 (M+H), (ES-) 405.16 (M-H); HPLC-Method A, Rt.2.80 min.
Example 100 (6-Methyl-lff-pyrazolo [3, 4-b]pyridin-3-yl) - [2- (2-trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (II- 100) : Prepared in DMF (11% yield) . XHNMR (500 MHz, DMSO- d6) δl3.2 (s, br, IH) , 10.8 (s, br, IH) , 8.57 (d, IH) , 7.95 (t, IH) , 7.82 (d, IH) , 7.72 (t, IH) , 7.65 (m, 2H) , 7.58 ( , 2H) , 2.44 (s, 3H, buried by DMSO) , 2.20 (s, 3H) ppm. LC-MS (ES+) 435.22 (M+H), (ES-) 433.25 (M-H); HPLC- Method A, Rt 2.94 min.
Example 101 (6-Oxo-5-phenyl-5 , 6-dihydro-lH-pyrazolo [4 , 3 - c] pyridazin-3 -yl) - [2- (2 -trif luoromethyl-phenyl) - quinazolin-4-yl] -amine 11-101: Prepared in DMF (6% yield). XHNMR (500 MHz, DMSO-d6) δ 12.6 (s, IH) , 11.0 (s, br, IH) , 8.60 (d, IH) , 7.95 (t, IH) , 7.88 (d, IH) , 7.80 (d, IH) , 7.68 (m, 4H) , 7.40 (s, 3H) , 7.22 (s, 2H) , 6.61 (s, IH) ppm. LC-MS (ES+) 500.21 (M+H), (ES-) 498.16 (M- H) ; HPLC-Method A, Rt 3.00 min.
Example 103 [6-Methyl-2- (2-trifluoromethoxy-phenyl) - pyrimidin-4-yl] - (5-phenyl-2H-pyrazol-3-yl) -amine (II- 103): MS 412.13 (M+H); HPLC-Method E Rt 1.248 min.
Example 104 (5-Furan-2-yl-2H-pyrazol-3-yl) - [6-methyl-2- (2-trifluoromethoxy-phenyl) -pyrimidin-4-yl] -amine (II- 104); MS.402.12 (M+H); HPLC-Method E, Rt 1.188 min.
Example 105 [6-Ethyl-2- (2-trifluoromethoxy-phenyl) - pyrimidin-4-yl] - (5-methyl-2H-pyrazol-3-yl) -amine (II- 105): MS 364.14 (M+H); HPLC-Method E, Rt 1.112 min.
Example 106 [2- (2-Chloro-phenyl) -pyrido [2, 3-d] pyrimidin- 4-yl] - (5-methyl-2ff-pyrazol-3-yl) -amine (11-106): XHNMR (500 MHz, DMSO) δl2.23 (s, IH) , 10.78 (s, IH) , 7.73-7.47 (m, 7H) , 6.72 (s, IH) , 2.21 (s, 3H) . MS: (M+H) 337.02. HPLC-Method A, Rt 2.783 min.
Example 107 (5-Fluoro-lH-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -6, 7-dihydro-5H- cyclopentapyrimidin-4-yl] -amine (11-107) : Prepared in 68% yield. XHNMR (-500MHz, DMSO-d6) δ 2.16 (t, 2H) , 2.88 (m, 2H) , 2.98 (t, 2H) , 7.21 (td, IH) , 7.29 (dd, IH) , 7.50
(dd, IH) , 7 . 65 (t , IH) , 7 . 67 (t , IH) , 7 . 73 (t , IH) , 7 . 79 (d, IH) , 10 .22 (br. s , IH) , 12 . 99 (br . s, IH) ; EI-MS 414 . 2 (M+H) ; HPLC-Method A, Rt 2 . 92 min. Example 108 (Iff-Indazol-3 -yl) - [2- (2-trifluoromethylphenyl) -pyrido [2, 3-d] pyrimidin-4-yl] -amine (11-108) :
HPLC-Method A, Rt 2.78 min. (95%); XHNMR (DMS0-d6, 500 MHz): 12.95 (IH, bs) , 11.45 δ 11.15(1H, bs) , 9.20 (2H, m) , 7.85-7.70 (2H, m) ,' 7.70-7.55 (4H, m) , 7.50 (IH, m) , 7.35 (IH, m) , 7.05 (IH, m) ; MS (m/z) 407.03 (M+H).
Example 109 (5, 7-Difluoro-Iff-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -pyrido [2, 3-d]pyrimidin-4-yl] - amine (11-109) : Yellow, di-TFA salt (25% yield) . HPLC (Method A) 3.10 min. (95%); XHNMR (DMSO-d6, 500 MHz) : 13.8-13.6 (IH, bs) , 11.4 - 11.2(1H, bs) , 9.15 (2H, m) , 7.85-7.75 (2H, m) , 7.75-7.62 (3H, m) , 7.32 (2H, m) ; MS (m/z) 442.98 (M+H) .
Example 110 [2- (2-Chloro-phenyl) -pyrido [2, 3-d] yrimidin- 4-yl] - (Iff-indazol-3-yl) -amine (11-110) : Prepared from 2 - aminonicotinic acid and 2-chlorobenzoyl chloride afforded the title compound as a di-TFA salt (28% yield) . HPLC- Method A, Rt 2.85 min. (95%); XHNMR (DMS0-d6, 500 MHz): 12.90 (IH, s) , 11.10 - 10.90 (IH, bs) , 9.05 (2H, m) , 7.75-7.60 (2H, m) , 7.51 (IH, m) , 7.45-7.25 (5H, m) ,. 6.95 (IH, m) ; MS (m/z) 372.99 (M+H).
Example 111 .(5-Fluoro-IH-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -5,6,7,8,9,10-hexahydro- cyclooctapyrimidin-4-yl] -amine (11-111). Prepared in 43% yield. XHNMR (500MHz, DMS0-d6) δ 1.46 (m, 2H) , 1.53 (m, 2H) , 1.77 (m, 4H) , 2.95 ( , 2H) , 3.04 ( , 2H) , 7.22 (m, 2H) , 7.50 (dd, IH) , 7.72 (m, 3H) , 7.80 (d, IH) , 10.5 (m, IH) , 13.05 (br s, IH) ; EI-MS 456.2 (M+H); HPLC-Method C, Rt 11.93 min. Example 112 [2- (2-Chloro-phenyl) -6,7-dihydro-5ff- cyclopentapyrimidin-4-yl] - (5-fluoro-Iff-indazol-3 -yl) - amine (11-112) : Prepared in 67% yield. XHNMR (500MHz, DMS0-d6) 82.18 (m, 2H) , 2.89 (m, 2H) , 3.02 (t, 2H) , 7.24
(td, IH) , 7.42 (m, 2H) , 7.49 (td, IH) , 7.52 (dd, IH) , 7.54 (d, IH) , 7.57 (dd, IH) , 10.50 (br. s, IH) , 13.06
(br . s , IH) ; EI -MS 380 . 1 (M+l ) ; HPLC-Method C , Rt 9 . 68 min .
Example 113 (lH-Indazol-3-yl) - [2- (2-trifluoromethylphenyl) -6,7-dihydro-5H-cyclopentapyrimidin-4-yl] -amine (11-113) : Prepared in 37% yield. XHNMR (50.0MHz, DMS0-d6) δ 2.65 ( , 2H) , 2.85 (m, 2H) , 2.99 (t, 2H) , 7.02 (t, IH) , 7.32 (t, IH) , 7.47 (d, IH) , 7.55 (d, IH) , 7.68 (t, IH) ,
7.74 (t, IH) , 7.80 (d, IH) , 10.37 (br. s, IH) , 12.91 (br. s, IH) ; EI-MS 396.1 (M+H); HPLC-Method B, Rt 9.88 min.
Example 114 (7-Fluoro-IH-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -6, 7-dihydro-5ff- cyclopentapyrimidin-4-yl] -amine (11-114): Prepared in 40% yield. XHNMR (500MHz, DMSO-d6) δ 2.15 (m, 2H) , 2.87 (m, 2H) , 2.97 (t, 2H) , 6.99 (td, IH) , 7.17 (dd, IH) , 7.38 (d, IH) , 7.65 (m, 2H) , 7.71 (t, IH) , 7.78 (d, IH) , 10.21 (br. s, IH) , 13.40 (br. s, IH) ; EI-MS 414.1 (M+H); HPLC-Method C, Rt 9.99 min.
Example 115 (5, 7-Difluoro-Iff-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -6, 7-dihydro-5ff- cyclopentapyrimidin-4-yl] -amine (11-115) : Prepared according to Method C in 52% yield. XHNMR (500MHz, DMSO- d6) δ 2.16 (m, 2H) , 2.89 (m, 2H) , 2.97 (t, 2H) , 7.19 (dd, IH) , 7.29 (td, IH) , 7.63 (t, IH) , 7.66 (d, IH) , 7.71 (t, IH) , 7.78 (d, IH) , 10.16 (br. s, IH) , 13.55 (br. s, IH) ; EI-MS 432.1 (M+H); HPLC-Method C, Rt 10.09 min.
Example 116 [2- (2-Chloro-phenyl) -6, 7 -dihydro-5ff- cyclopentapyrimidin-4-yl] - (Iff-indazol-3 -yl) -amine (II- 116): Prepared in 56% yield. XHNMR (500MHz, DMSO-d6) δ 2.16 ( , 2H) , 2.85 (m, 2H) , 3.01 (t, 2H) , 7.06 (t, IH) , 7.34 (t, IH) , 7.40 (t, IH) , 7.48 (m, 2H) , 7.53 (d, IH) , 7.56 (d, IH) , 7.63 (d, IH) , 10.39 (br. s, IH) , 12.91 (s, IH) ; EI-MS 362.1 (M+H); HPLC-Method A, Rt 3.09 min.
Example 117 [2- (2-Chloro-phenyl) -6, 7-dihydro-5ff- cyclopentapyrimidin-4-yl] - (7-fluoro-Iff-indazol-3-yl) - amine (11-117) : Prepared in 63% yield. XHNMR (500MHz, DMS0-d6) δ 2.15 (m, 2H) , 2.87 (m, 2H) , 3.00 (t, 2H) , 7.01 (td, IH) , 7.19 (dd, IH) , 7.39 (t, IH) , 7.45 (m, 2H) , 7.51 (d, IH) , 7.55 (d, IH) , 10.35 (br. s, IH) , 13.45 (br. s, IH) ; EI-MS 380.1 (M+H); HPLC-Method A, Rt Rt 3.15 min.
Example 118 [2- (2-Chloro-phenyl) -6, 7 -dihydro-5ff- cyclopentapyrimidin-4-yl] - (5, 7-difluoro-Iff-indazol-3-yl) - amine (11-118) : Prepared in 60% yield. XHNMR (500MHz, DMS0-d6) δ 2.18 (m, 2H) , 2.91 (m, 2H) , 3.01 (t, 2H) , 7.32 (t, IH) , 7.33 (td, IH) , 7.41 (t, IH) , 7.48 (t, IH) , 7.53 (d, IH) , 7.55 (dd, IH) , 10.35 (br. s, IH) , 13.45 (br. s, IH) ; EI-MS 398.1 (M+H); HPLC-Method A, Rt Rt 3.24 min.
Example 119 (Iff-Indazol-3 -yl) - [2- (2-trifluoromethylphenyl) -5, 6,7, 8,9,10-hexahydro-cyclooctapyrimidin-4-yl] - amine (11-119) : Prepared in 36% yield. XHNMR (500MHz,
DMS0-d6) δ 1.47 (m, 2H) , 1.53 (m, 2H) , 1.78 (m, 4H) , 2.96 (m, 2H) , 3.06 (t, 2H) , 7.03 (t, IH) , 7.47 (t, IH) , 7.72 (d, IH) , 7.73 (d, IH) , 7.72 (m, 3H) , 7.81 (d, 1H),.10.52 (m, IH) ,. 12.97 (br. s, IH) ; EI-MS 438.2 (M+l) ; HPLC- Method A, Rt 3.37 min.
Example 120 (7-Fluoro-lH-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -5, 6, 7, 8, 9, 10-hexahydro- cyclooctapyrimidin-4-yl] -amine (11-120) : Prepared in 40% yield. XHNMR (500MHz, DMS0-d6) δ 1.46 (m, 2H) , 1.52 (m, 2H) , 1.77 (m, 4H) , 2.94 (m, 2H) , 3.04 (m, 2H) , 7.00 (td, IH) , 7.17 (dd, IH) , 7.30 (d, IH) , 7.70 (m, 3H) , 7.79 (d, IH) , 10.5 (m, IH) , 13.49 (br s, IH) ; EI-MS 456.1 (M+H); HPLC-Method A, Rt 3.43 min.
Example 121 (5, 7-Difluoro-lff-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -5, 6,7, 8, 9, 10-hexahydro- cyclooctapyrimidin-4-yl] -amine (11-121): Prepared in 48% yield. XHNMR (500MHz, DMSO-d6) δ 1.46 (m, 2H) , 1.52 (m, 2H) , 1.77 (m, 4H) , 2.95 (m, 2H) , 3.03 (m, 2H) , 7.14 (d, IH) , 7.30 (t, IH) , 7.73 (m, 3H) , 7.80 (d, IH) , 10.5 (m, IH) , 13.62 (br. s, IH) ; EI-MS 475.1 (M+l); HPLC-Method A, Rt 3.52 min.
Example 122 [6-Cyclohexyl-2- (2-trif luoromethyl-phenyl) - pyrimidin- -yl] - ( Iff- indazol- 3 -yl) -amine (11-122) :
Prepared in 45% yield. XHNMR (500 MHz, CDC13) δ 1.30 (2H, m) , 1.46 (2H, m) , 1.65 (2H, m) , 1.76 (2H, m) , 1.91 (2H, m) , 2.61 (IH, br m) , 7.08 (IH, t, J=7.4 Hz) , 7.27' (IH, d, J=8.0 Hz) , 7.35 (IH, t, J= 7.1 Hz) , 7.50 (IH, t, J=7.0 Hz) , 7.58 (IH, t, J=7.4 Hz) , 7.66 (3H, m) , 7.72 (IH, d, J=7.8 Hz), 8.0 (IH, br) , 9.87 (IH, br) ppm; HPLC-Method D, Rt 3.57 min; LC-MS 438.17 (M+H) +
Example 123 [6- (2 -Fluoro -phenyl) -2- (2-trif luoromethylphenyl) -pyrimidin-4-yl] - ( IH- indazol- 3 -yl) -amine (11-123) : Prepared in 8% yield. XHNMR (500 MHz, CDC13) δ 7.18 (3H, m) , 7.37 (IH, m) , 7.43 (IH, t,. J=7.9 Hz) , 7.51 (IH, d, J=7.9 Hz) , 7.55 (IH, t, J=7.6 Hz) , 7.65 (IH, t, J=7.4 Hz) , 7.79 (IH, d, J=7.9 Hz) , 7.85 (IH, d, J= 7.6 Hz) , 8.19 (2H, m) , 8.70 (IH, d, J= 8.5 Hz) ppm; HPLC-Method D, Rt 4.93 min; LC-MS 450.13 (M+H) +
Example 124 (6-Fluoro-Iff-indazol-3 -yl) - [2- (2- trifluoromethyl-phenyl) -quinazolin-4-yl] -amine (11-124) . Prepared in DMF (87% yield) as yellow solid. XHNMR (500 MHz, DMSO-d6) δl3.0 (s, IH) , 11.1 (s, br, IH) , 8.66 (d, IH) , 7.95 (t, IH) , 7.80 (d, 1H), .7.72 (m, 2H) , 7.62 (m, 4H) , 7.21 (dd, IH) , 6.84 (td, IH) ppm. LC-MS (ES+) 424.15 (M+H); HPLC-Method A, Rt 3.05 min.
Example 125 3- [2- (2-Trifluoromethyl-phenyl) -quinazolin-4- ylamino] -Iff-indazole-5-carboxylic acid methyl ester (II- 125): To a solution of compound 11-79 (100 mg 0.21 mmol) in DMF (2 mL) was added MeOH (1 mL) , DIEA (54 uL, 0.31 mmol) and PdCl2(dppf) (4 mg, 0.005 mmol). The flask was flushed with CO three times and then charged with a CO balloon. The reaction mixture was heated at 80°C for 14 h then poured into water. The resulting precipitate was collected and washed with water. The crude product was then purified first by flash column (silica gel, 50%
■ ethyl acetate in hexanes) then by preparative HPLC to to afford 11-125 (32%) as yellow solid. XHNMR (500 MHz,
DMSO-d6) δl3.3 (s, IH) , 11.3 (s, br, IH) , 8.70 (d, IH) , 8.36 (s, IH) , 7.97 (t, IH) , 7.82 (m, 2H) , 7.71 (m, 3H) , 7.58 (m, 2H) , 7.51 (d, IH) , 3.75 (s, 3H) ppm; LC-MS (ES+) 464.13 (M+H); HPLC-Method A, Rt 3.12 min. Example 208 (5-Methyl-2ff-pyrazol-3-yl) - [2- (2-naphthyl-1- yl) -quinazolin-4-yl] -amine (11-208): XHNMR (500 MHz, DMSO- άβ) δ8.92 (s, IH) , 8.73 (m, IH) , 8.39 (m, IH) , 8.09 (m, 2H) , 7.95 (m, 3H) , 7.62 (m, 3H) , 6.78 (s, IH) , 2.32 (s, 3H) ; MS 352.2 (M+H) .
Example 209 [2- (2-Chloro-phenyl) -pyrido [2, 3-d] pyrimidin- 4-yl] - (7-fluoro-lff-indazol-3-yl) -amine (11-214): Prepared from 4-Chloro-2- (2-chloro-phenyl) -pyrido[2, 3-d] pyrimidine (100 mg, 0.36mmol) and 7-Fluoro-Iff-indazol-3-ylamine (108mg, 0.72mmol). Purification by preparative HPLC afforded the title compound as a yellow, di-TFA salt (93 mg, 46% yield). HPLC-Method A, Rt 3.04 min; XH. NMR- (DMSO, 500 MHz): δ 13.67 (IH, s) , 11.40-11.25 (IH, bs) , 9.35- 9.25 (2H, m) , 7.95 (IH, m) , 7.80-7.47 (5H, m) , 7.35(1H, m) , 7.15 (IH, m) ; MS (m/z), MH+ 391.1.
Example 210 [2- (2-Chloro-phenyl) -pyrido [2, 3-d] pyrimidin- 4-yl] - (5-fluoro-Iff-indazol-3-yl) -amine (11-215): Prepared from 4-Chloro-2- (2-chloro-phenyl) -pyrido [2, 3-d] pyrimidine (100 mg, 0.36mmol) and 5-Fluoro-lff-indazol-3- ylamine (108mg, 0.72mmol). Purification by preparative HPLC afforded the title compound as a yellow, di-TFA salt (45 mg, 22% yield). HPLC-Method A, Rt 3.00 min; XH NMR (DMSO, 500 MHz): δ 13.0 (IH, s) , 10.90(1H, bs) , 9.15-9.05 (2H, m) , 7.70 (IH, m) , 7.60-7.30 (6H, m) , 7.20 (IH, m) ; MS (m/z) , MH+ 391.1.
Example 211 [2- (2-Chloro-phenyl) -pyrido [2, 3-d] pyrimidin- 4-yl] - (5, 7-difluoro-lff-indazol-3-yl) -amine (11-216):
Prepared from 4-Chloro-2- (2-chloro-phenyl) -pyrido [2 , 3- d] pyrimidine (100 mg, 0.36mmol) and 7-Difluoro-lH- indazol-3-ylamine (112mg, 0.66mmol). Purification by preparative HPLC afforded the title compound as a yellow, di-TFA salt (130 mg, 62% yield). HPLC-Method A, Rt 3.12 min; XH NMR (DMSO, 500 MHz): 13.80-13.60 (IH, bs) , 11.30- 11.10 (IH, bs) , 9.20-9.10 (2H, m) , 7.80 (IH, m) , 7.60- 7.30 (6H, m) ; MS (m/z), MH+ 409.1.
Example 212 [2- (2-Chloro-phenyl) -pyrido [3, 4-d] pyrimidin- 4-yl] - (Iff-indazol-3-yl) -amine (11-217): Prepared from 4- Chloro-2- (2-chloro-phenyl) -pyrido [3 , -d] pyrimidine (100 mg, 0.36mmol) and Iff-indazol-3-ylamine (88mg, 0.66mmol) Purification by preparative HPLC afforded the title compound as a yellow, di-TFA salt (72 mg, 33% yield) . HPLC-Method A, Rt 3.21 min XH NMR (DMSO, 500 MHz) : δ 12.95 (IH, s) , 10.90 (IH, bs) , 9.25 (IH, s) , 8.75 (IH, m) , 8.55 (IH, m) , 7.65 (IH, m) , 7.55 (IH, m) , 7.50-7.30 (5H, m) , 7.00 (IH, m) ; MS (m/z), MH+ 373.1.
Example 213 [2- (2-Chloro-phenyl) -pyrido [3, 4-d] pyrimidin- 4-yl] - (7-fluoro-Iff-indazol-3-yl) -amine (11-218): Prepared from 4-Chloro-2- (2-chloro-phenyl) -pyrido [3 , 4-d] pyrimidine (100 mg, 0.36mmol) and 7-Fluoro-Iff-indazol-3 -ylamine (108mg, 0.72mmol) . Purification by preparative HPLC afforded the title compound as a yellow, di-TFA salt (48.7 mg, 22% yield). HPLC-Method A, Rt 3.35 min; XH NMR (DMSO, 500 MHz): δ 12.95 (IH, s) , 10.90 (IH, bs) , 9-25 (IH, s) , 8.75 (IH, m) , 8.55 (IH, m) , 7.70-7.35 (5H, m) , 7.25 (IH, m) , 6.95 (IH, m) , ; MS (m/z), MH+ 391.08.
Example 214 [2- (2-Chloro-phenyl) -pyrido [3, 4-d] pyrimidin- 4-yl] - (5-fluoro-lH-indazol-3-yl) -amine (11-219): Prepared from 4-chloro-2- (2-chloro-5-fluoro-IH-indazol-3-ylamine (108mg, 0.72mmol) . Purification by preparative HPLC. afforded the title compound as a yellow, di-TFA salt (57.2 mg, 26% yield) . HPLC-Method A, Rt 3.27 min; XH NMR (DMSO, 500 MHz) : δ 13.05 (IH, s) , 10.95 (IH, s) , 9.25 (IH, S) , 8.75 (IH, m) , 8.55 (IH, m) ,' 7.60 (IH, m) , 7.55 • (IH, m) , 7.50-7.30 (5H, m) , 7.25 (IH, m) ; MS (m/z) , MH+ 391.1.
Example 215 [2- (2-Chloro-phenyl) -pyrido [3,4-d] yrimidin- 4-yl] - ( 5, 7 -di fluoro -Iff- indazol- 3 -yl) -amine (11-220) :
Prepared from 4-chloro-2- (2-chloro-7-dif luoro -Iff- indazol - 3-ylaτnine (112mg, 0.66mmol) . Purification by preparative HPLC afforded the title compound as a yellow, di-TFA salt (57.2 mg, 26% yield) . HPLC-Method A, Rt 3.45 min; XH NMR (DMSO, 500 MHz) : δ 13.65 (IH, s) , 11.0 (IH, s) , 9.25 (IH, s) , 8.80 (IH, m) , 8.50 (IH, m) , 7.60 (IH, ) , 7.55 (IH, m) , 7.50-7.30 (5H, m) ; MS (m/z) , MH+ 409.1.
Example 216 6 -Fluoro -Iff- indazol -3 -ylamine (Al) : XHNMR (500 MHz, DMSO-d6) δll.4 (s, IH) , 7.68 (dd, IH) , 6.95 (dd, IH) , 6.75 (td, IH) , 5.45 (s, 2H) ppm; LC-MS (ES+) 152.03 (M+H) ; HPLC-Method A, Rt 2.00 min.
Example 217 5 -Fluoro -Iff- indazol -3 -ylamine (A2) : XHNMR (500 MHz, DMSO-d6) δll.3 (s, IH) , 7.43 (d, IH) , 7.22 (m, IH) , 7.08 (m, IH) , 5.29 (s, 2H) ppm; LC-MS (ES+) 152.01 (M+H) ; HPLC-Method A, Rt 1.93 min.
Example 218 5,7-Dif luoro-lH-indazol-3-yl-amine (A3) : XHNMR (500 MHz, CD3OD) δ7.22 (dd, J=2.0, 8.45Hz, IH) , 7.04-6.87 (m, IH) ; LC-MS (ES+) 169.95 (M+H) ; HPLC-Method C, Rt 2.94 min
Example 219 7 -Fluoro -Iff- indazol -3 -ylamine (A4) : XHNMR (500 MHz. DMSO-d6) δll.8 (s, IH) , 7.42 (d, IH) , 6.97 (m, IH) , 6.78 (m, IH) , 5.40 (s, 2H) ppm;' LCMS (ES+) 152.01 (M+H) ; HPLC-Method A, R 2.00 min.
Example 220 7-Fluoro-6-trifluoromethyl-Iff-indazol-3- ylamine (A5) : XH-NMR (500 MHz, DMSO) δ 12.5 (s, IH) , 7.75 (d, IH) , 7.25 (m, IH) , 5.85 (m, IH) ppm; MS (FIA) 220.0 (M+H); HPLC-Method A, Rt 2.899 min.
Example 221 6-Bromo-Iff-indazol-3-ylamine (A6) : XH-NMR (500 MHz, DMSO) δ 11.5 (s, IH) , 7.65 (d, IH) , 7.40 (s,. IH) ,
7.00 (d, IH) , 5.45 (br s, IH) ppm; MS . (FIA) 213.8 (M+H); HPLC-Method A, Rt 2.441 min.
Example 222 4-Fluoro-lff-indazol-3-ylamine (A7) : XH-NMR (500 MHz, DMSO) δ 11.7 (s, IH), 7.17 (m, IH) , 7.05 (d,
IH) , 6.7 (br, IH) , 6.60 (dd, IH) , 5.20 (br s, 2H) ppm; MS (FIA) 152.0 (M+H); Method A, Rt 2.256 min.
Example 223 5-Bromo-lff-indazol-3-ylamine (A8) : XH-NMR (500 MHz, DMSO) δ 11.55 (br s, IH) , 7.95 (s, IH) , 7.30 (d, IH) , 7.20 (d, IH) , 5.45 (br s, 2H) ppm; MS (FIA) 213.8 (M+H); Method A, Rt 2.451 min.
Example 224 5-Nitro-Iff-indazol-3 -ylamine (A9) : XH-NMR (500 MHz, DMSO-d6) δ 9.00 (s, IH) , 8.20 (d, IH) , 7.45 (d, IH) , 6.15 (br s, IH) ppm; Method A, Rt 2.184 min
Example 225 4 -Pyrrol-1-yl-Iff-indazol-3 -ylamine (A10) : XH-
NMR (500 MHz, DMSO) δ 7.20 (s, 2H) , 7.00 (s, 2H) , 6.75 (m, IH) , 6.25 (s, 2H) , 4.30 (d, IH) ppm; Method A, Rt 2.625 min. Example 226 4-Chloro-5, 6-dimethyl-2- (2-trifluoromethylphenyl) -pyrimidine (Bl) : Prepared to afford a colorless oil in 75% yield. XH-NMR (500 MHz, CDC13) 6 7.70 (d, J=7.8 Hz, IH) , 7.64 (d, J=7.6 Hz, IH) , 7.55 (t, J=7.6 Hz, IH) , 7.48 (t, J=7.5 Hz, IH) , 2.54 (s, 3H) , 2.36 (s, 3H) ppm; MS (FIA) 287.0 (M+H); HPLC-Method A, Rt 3.891 min.
Example 227 4-Chloro-2- (2-chloro- henyl) -5, 6-dimethyl- pyrimidine (B2) : Prepared to afford a yellow-orange oil in 71% yield. XH-NMR (500 MHz, CDC13) δ 7.73 (m, IH) , 7.52 (m, IH) , 7.39 (m, 2H) , 2.66 (s, 3H) , 2.45 (s, 3H) ppm; MS (FIA) 253.0 (M+H); HPLC-Method A, Rt Rt 4.156 min.
Example 228 4-Chloro-6-methyl-2- (2-trifluoromethyl- phenyl) -pyrimidine (B3) : Prepared to afford a pale yellow • oil in 68% yield. XH-NMR (500 MHz, CDC13) δ 7.72 (d, J=7.8 Hz, IH) , 7.65 (d, J=7.9 Hz, IH) , 7.57 (t, J=7.5 Hz, IH) , 7.52 (t, J=7.8 Hz, IH) , 7.16 (s, IH) , 2.54 (s, 3H) ppm; MS (FIA) 273.0 (M+H); HPLC-Method A, Rt 3.746 min.
Example 229 4-Chloro-6-cyclohexyl-2- (2-trifluoromethylphenyl) -pyrimidine (B4) : Prepared to afford a yellow oil in 22% yield. XH-NMR (500 MHz, CDC13) δ 7.70 (m, 2H) , 7.57 (t, J=7.5 Hz, IH) , 7.50 (t, J=7.5 Hz, IH) , 7.19 (s, IH) , 2.65 (m, IH) , 1.9 (m, 2H) , 1.8 (m, 2H) , 1.5 (m, 2H) , 1.3 (m,- 2H), 1.2 (m, 2H) ppm; MS (FIA) 341.0 (M+H).
Example 230 4-Chloro-6-phenyl-2- (2-trifluoromethylphenyl) -pyrimidine (B5) : Prepared to afford a yellow oil in 53% yield. XH-NMR (500 MHz, CDC13) δ 8.08 (dd, J=7.9, 1.6 Hz, 2H) , 7.80 (d, J=7.6 Hz, IH) , 7.77 (d, J=7.8 Hz, IH) , 7.67 (s, IH) , 7.61 (t, J=7.5 Hz, IH) , 7.54 (t, J=7.6 Hz, IH) , 7.47 (m, 3H) ppm; MS (FIA) 335.0 (M+H); HPLC- Method A, Rt 4.393 min.
Example 231 4-Chloro-2- (2,4-dichloro-phenyl) -5,6- dimethyl-pyrimidine (B6) : Prepared to afford a white solid in 91% yield. XH-NMR (500 MHz, CDC13) δ 7.62 (d, J=8.3 Hz, IH) , 7.43 (d, J=7.0 Hz, IH) , 7.27 (dd, J=8.3, 2.0 Hz, IH) , 2.55 (s, 3H) , 2.35 (s, 3H) ppm; MS (FIA) 287, 289 (M+H); HPLC-Method A, Rt 4.140 min.
Example 232 4-Chloro-6- (2-chloro-phenyl) -2- (2- trifluoromethyl-phenyl) -pyrimidine (B7) : Prepared to affod a yellow oil in 52% yield. XH-NMR (500 MHz, CDC13) δ 7.75 ( , 3H) , 7.65 (m, 2H) , 7.53 (m, IH) , 7.44 (m, IH) , 7.36 (m, 2H) ppm; MS (FIA) 369.1 (M+H); HPLC-Method A, Rt 4.426 min.
Example 233 4-Chloro-6- (2-fluoro-phenyl) -2- (2- trifluoromethyl-phenyl) -pyrimidine (B8) : Prepared to afford a yellow oil in 95% yield. XH-NMR (500 MHz, CDC13) δ 8.24 (t, J=7.9 Hz, IH) , 7.84 (s, IH) , 7.78 (d, J=7.7 Hz, IH), 7.76 (d, J=8.0 Hz, IH) , 7.60 (t, J=7.5 Hz, IH) , 7.53 (t, J=7.6 Hz, IH) , 7.43' (m, IH) , 7.23 (t, J=7.6 Hz, IH) , 7.13 (m, IH) ppm; MS (FIA) 353.0 (M+H).
Example 234 4-Chloro-6-pyridin-2-yl-2- (2-trifluoromethylphenyl) -pyrimidine (B9) : Prepared to afford a pale yellow solid in 50% yield. XH-NMR (500 MHz, CDC13) δ 8.68 (m, IH) , 8.48 (dd, J=7.9, 0.8 Hz, IH) , 8.38 (d, J=2.3 Hz, IH) , 7.84 (m, 3H) , 7.62 (t, J=7.6 Hz, IH) , 7.55 (t, J=7.6 Hz, IH) , 7.38 (m, IH) ppm; MS (FIA) 336.0 (M+H); HPLC- Method A, Rt 4.575 min. Example 235 6-Benzyl-4-chloro-2- (2-trifluoromethylphenyl) -5, 6,7, 8-tetrahydro-pyrido [4, 3-d] pyrimidine (BIO) :
XHNMR (500 MHz, CDC13) δ7.70 (d, IH) , 7.62 (d, IH) , 7.55 (t, IH) , 7.48 (t, IH) , 7.32 (m, 4H) , 7.25 (m, IH) , 3.74 (s, 2H) , 3.66 (s, 2H) , 2.99 (t, 2H) , 2.80 (t, 2H) ppm; LCMS (ES+) 404.17 (M+H); HPLC-Method A, Rt 3.18 min.
Example 236 7-Benzyl-4-chloro-2- (2-trifluoromethylphenyl) -5, 6, 7, 8-tetrahydro-pyrido [3, 4-d] pyrimidine (BID : XHNMR (500 MHz, CDCl3) δ7.69 (d, IH) , 7.60 (d, IH) , 7.54 (t, IH) , 7.47 (t, IH) , 7.28 (m, 4H) , 7.20 (m, IH) , 3.68 (s, 2H) , 3.67 (s, 2H) , 2.86 (t, 2H) , 2.79 (t, 2H) ppm. MS (ES+) 404.18 (M+H); HPLC-Method A, Rt 3.12 min.
Example 237 4-Chloro-2- (4-fluoro-2-trifluoromethylphenyl) -quinazoline (B12) : XHNMR (500MHz, CD3OD) δ 8.43 (d, J=8.1Hz, IH) , 8.20-8.05 (m, 2H) , 8.05-7.82 (m, 2H) , 7.71-7.51 (m, 2H) . LC-MS (ES+) 327.09 (M+H). HPLC-Method D, Rt 4.56 min.
Example 238 4-Chloro-2- (2-chloro-5-trifluoromethylphenyl) -quinazoline (B13) : LC-MS (ES+) 342.97 (M+H). HPLC-Method D, Rt 4.91 min.
Example 239 4-Chloro-2- (2-chloro-4-nitro-phenyl) - quinazoline (B14) : LC-MS (ES+) 319.98 (M+H). HPLC-Method D, Rt 4.45 min.
Example 240 4-Chloro-2- (2-trifluoromethyl-phenyl) - quinazoline (B15) : Prepared in 57% yield. White solid.
XHNMR (500MHz, DMS0-d6) δ 7.79 (t, IH) , 7.86 (t, IH) , 7.94 (m, 3H) , 8.15 (dd, IH) , 8.20 (td, IH) , 8.37 (m, IH) ; EI- MS 308.9 (M) . Example 241 4-Chloro-2- (2-trifluoromethyl-phenyl) -6,7- dihydro-5ff-cyclopentapyrimidine (B16) : Prepared in 22% yield. XHNMR (500MHz, DMSO-d6) δ 2.19 (m, H) , 3.01 (t, 2H) , 3.08 (t, 2H) , 7.49 (t, IH) , 7.55 (t, IH) , 7.62 (d, IH) , 7.71 (d, IH) . EI-MS 299.0 (M+H).
Example 242 4-Chloro-2- (2-chloro-phenyl) -6,7,8,9- tetrahydro-5ff-cycloheptapyrimidine (B17) : Prepared according to Method C in 82% yield to afford a white solid. XHNMR (500MHz, CDCl3) δ 1.67 (m 4H) , 1.87 (m 2H),, 3.02 (m 4H) , 7.28 (m, 2H) , 7.40. (m, IH) , 7.65 (m, IH) ; EI-MS 293.0 (M+l) .
■ Example 243 4 -Chloro-2- (2-trifluoromethyl-phenyl) - 5, 6,7, 8, 9, 10-hexahydro-cyclooctapyrimidine (B18) :
Prepared in 38% yield to afford a brown oil. XHNMR (500MHz, CDC13) δ 1.35 (m 2H) , 1.41 (m 2H) , 1.76 (m 4H) , 2.96 (m, 4H) , 7.48 (t, IH) , 7.56 (t, IH),.7.66 (d, IH) , 7.70 (d, IH) ; EI-MS 341.0 (M+l).
Example 244 4-Chloro-8-methoxy-2- (2-trifluoromethylphenyl) -quinazoline (B19) : Prepared from 8-methoxy-2- (2- trifluoromethyl-phenyl) -3ff-quinazolin-4-one (l.Og, 3.12mmol), triethylamine hydrochloride (472mg, 3.43mmol), and POCI3. Purification by flash chromatography afforded a white solid (89% yield) . HPLC-Method A, Rt 4.10 min, (98%), MS (m/z) 258.08 (M+H).
Example 245 2- (4-Chloro-quinazplin-2-yl) -benzonitrile
(B20) : Prepared to afford a yellow solid in 1.5% yield. XH-NMR (500 MHz, CDC13) δ 8.47 (d, IH) , 8.24 (d, IH) , 8.16 (d, IH) , 8.07 (impurity), 7.94 (t, IH) , 7.92 (impurity), 7.86 (d, IH) , 7.68 (m, 2H) , 7.65 (impurity), 7.54 (impurity), 7.49 (t, IH) , 4.2 (impurity), 1.05 (impurity) ppm; MS (LC/MS) 266.05 (M+H); HPLC-Method A, Rt 3.88 min.
Example 246 6-Methyl-2- (2-trifluoromethyl-phenyl) -3ff- pyrimidin-4-one (D3) : Prepared to afford a yellow solid in 50% yield. XH-NMR (500 MHz, DMSO-d6) δ 12.7 (br s, IH) , 7.9 (m, IH) , 7.8 (m, 2H) , 7.7 (m, IH) , 6.3 (s, IH) , 2.21 (s, 3H) ppm; MS (FIA) 255.0 (M+H); HPLC-Method A, Rt 2.578 min.
Example 247 6-Cyclohexyl-2- (2-trifluoromethyl-phenyl) -3ff- pyrimidin-4-one (D4) : Prepared to afford an off-white solid in 54% yield. XH-NMR (500 MHz, DMS0-d6) δ 12.9 (br s, IH) , 7.9 (m, 4H) , 6.3 (s, IH) , 2.5 (m, IH) , 1.9 (m, 5H) , 1.4 (m, 5H) ppm; MS (FIA) 323.1 (M+H); HPLC-Method A, Rt 3.842 min.
Example 248 2- (2-Chloro-5-trifluoromethyl-phenyl) -3H- quinazoli-4-one (D10) : XHNMR (500MHz, CD3OD) δ 8.32-8.25 (m, IH) , 8.01 (s, IH) , 7.91-7.72 (m, IH) , 7.66-7.55 (m, IH) . LC-MS (ES+) 325.01 ' (M+H) . HPLC-Method D, Rt 3.29 min.
Example 249 2- (4-Fluoro-2-trifluoromethyl-phenyl) -3ff- quinazolin-4-one (D14) : XHNMR (500MHz, CD30D) δ 8.28 (d, 8.0Hz, IH) , 7.94-7.84 (m, IH) , 7.84-7.77 (m, IH) , 7.76- 7.67 (m, 2H) , 7.65-7.53 ( , 2H) . LC-MS (ES+) 309.06 (M+H). HPLC-Method D, Rt 2.88 min.
Example 250 2 - ( 4 -Nitro-2 -chloro -phenyl) -3H-quinazolin-4 - one (D15) : LC-MS (ES+) 302 . 03 (M+H) . HPLC-Method D , Rt 2 . 81 min . Example 251 2- (5-Fluoro-2-trifluoromethyl-phenyl) -3ff- quinazolin-4-one (D17) : XHNMR (500MHz, CD3OD) δ 8.28 (d, Rt J=8.05Hz, IH) , 7.96 (dd, J=5.05, 8.55Hz, IH) , 7.89 (t, J=7.9Hz, IH) , 7.78-7.69 (m,lH), 7.66-7.46 (m, 3H) . LC-MS (ES+) 309.14 (M+H). HPLC-Method D, Rt 2.90 min.
Example 252 (Iff-Indazol-3-yl) - (2-phenyl-quinazolin-4-yl) - amine (III-l) : Prepared by Method A in DMF to afford 70 mg (50% yield) as pale yellow solid. XH NMR (500 MHz,
DMSO-d6) δl3.1 (s, br, IH) , 8.48 (d, IH) , 7.91 (d, 2H) , 7.76 (br, 2H) , 7.45 (m, 2H) , 7.36 (d, IH) , 7.20 (m, 4H) , 6.86 (t, IH) ppm. MS (ES+) 338.07 (M+H); (ES-) 336.11 (M- H) ; HPLC-Method A, Rt 2.88 min.
Example 253 (5-Methyl-2ff-pyrazol-3-yl) - (2-phenyl-5, 6, 7, 8- tetrahydroquinazolin-4-yl) -amine (III-7) : Prepared according to Method A. XH NMR (500 MHz, DMSO-d6) δ 12.1 (s, br, IH) , 8.70 (s, br, IH) , 8.37 (d, J = 6.7 Hz, 2H) , 7.54 (m, 3H) , 6.67 (s, IH) , 2.82 (m, 2H) , 2.68 (m, 2H) , 2.37 (s, 3H) , 1.90 (s, br, 4H) ; MS 306.1 (M+H).
Example 254 (5-Methyl-2ff-pyrazol-3-yl) - (2 -phenyl-6, 7, 8, 9- tetrahydro-5ff-cycloheptapyrimidin-4-yl) -amine (III-8) : MS 320.48 (M+H); HPLC-Method E, Rt 1.124 min.
Example 255 (5-Methyl-2ff-pyrazol-3-yl) - (2-pyridin-4-yl- quinazolin-4-yl) -amine (III-9) : Yellow solid, mp 286- 289°C, XH NMR (DMSO) δ 2.35 (3H, s) , 6.76 (IH, s) , 7.61 (IH, m) , 7.89 (2H, m) , 8.32 (2H, d) , 8.70 (IH, d) , 8.78 (2H, d) , 10.56 (IH, br s) , 12.30 (IH, br s) ; IR (solid) 1620, 1598, 1571, 1554, 1483, 1413, 1370, 1328; MS 303.2 (M+H) + Example 256 (7-Chlorσ-2-pyridin-4-yl-quinazolin-4-yl) - (5- methyl-2ff-pyrazol-3-yl) -amine (111-28) : XH NMR (DMSO-d6) δ 2.35 (3H,s), 6.75 (IH, s) ,. 7.65 (IH, d) , 7.93 (IH, s) , 8.30 (2H, d) , 8.73 (IH, d) , 8.79 (2H, d) , 10.69 (IH, s) , 12.33 (IH, s) ; MS m/z 337.2 (M+H)+.
Example 257 (6-Chloro-2-pyridin-4-yl-quinazolin-4-yl) - (5- methyl-2ff-ρyrazol-3-yl) -amine (111-29) : XH NMR (DMSO-d6) δ 2.31 (3H, S), 6.74 (lH,s), 7.89 (IH, s) , 8.30 (2H, d) ,
8.80 (2H, d) , 8.91 (IH, s) , 10.63 (IH, s) , 12.29 (IH, s) ; MS 337.2 (M+H)+.
Example 258 (2-Cyclohexyl-quinazolin-4-yl) - (5-methyl-2ff- pyrazol-3-yl) -amine (111-30) : XH NMR (DMSO) δ 2.35 (3H, s) , 1.70 (3H, m) , 1.87 (2H, d), 1.99 (2H, d) , 2.95 (IH, t), 6.72 (IH, s), '7.75 (IH, d) , 7.88 (IH, s) , 7.96 (IH, s) , 8.83 (IH, s) , 11.95 (IH, s) , 12.70 (IH, s) ; MS 308.4 (M+H)+.
Example 259 (5-Methyl-2ff-pyrazol-3-yl) - (2-phenyl- quinazolin-4-yl) -amine (111-31) : mp 246°C; XH NMR (400MHz) δ 2.35 (3H, s) , 6.70 (IH, br s) , 7.51-7.57 (4H, m) , 7.83- 7.84 (2H, d) , 8.47-8.50 (2H, d) , 8.65 (IH, d) , 10.4 (IH, s) , 12.2 (IH, bs) ; IR (solid) 3696, 3680, 2972, 2922, 2865; MS 302.1 (M+H) + .
Example 260 [2- (4-Iodophenyl) -quinazolin-4-yl] - (5-methyl- 2ff-pyrazol-3-yl) -amine (111-32) : XH NMR (DMSO-d6) δ 2.34 (3H, s) , 6.72 (IH, s) , 7.56 (IH, d) , 7.84 (2H, d) , 7.93
(2H, d) , 8.23 (2H, d) , 8.65 (IH, s) , 10.44 (IH, s) , 12.24
(IH, S) ; MS 428.5 (M+H)+. Example 261 [2- (3,4-Dichlorophenyl) -quinazolin-4-yl] - (5- methyl-2ff-pyrazol-3-yl) -amine (111-33) : A suspension of 2- (3, 4-dichloro-phenyl) -3ff-quinazolin-4-one (lg, 3.43 mmol) in phosphorus oxychloride (4 mL) was stirred at 110°C for 3 hours. The solvent was removed by evaporation and the residue is treated carefully with cold aqueous, saturated NaHC03. The resulting solid was collected by filtration and washed with ether to afford 4-chloro-2- (3, 5-dichloro-phenyl) -quinazoline as a white solid (993 mg, 93%) . To the above compound (400mg, 1.29 mmol) in THF (30 mL) was added 3-amino-5-methyl pyrazole (396 mg, 2.58 mmol) and the resulting mixture heated at 65°C overnight . The solvents were evaporated and the residue triturated with ethyl acetate, filtered, and washed with the minimum amount of ethanol to afford compound 111-33 as a white solid (311 mg 65%): mp 274°C; XH NMR (DMSO) δ 2.34 (3H, s) , 6.69 (IH, s) , 7.60 (IH, m) , 7.84 (IH, d) , 7.96 (2H, d) , 8.39 (IH, dd) , 8.60 (IH, d) , 8.65 (IH, d) , 10.51 (IH, s) , 12.30 (IH, s) ; IR (solid) 1619, 1600, 1559, 1528, 1476, 1449, 1376, 1352, 797, 764, 738; MS 370.5 (M+H)+.
Example 262 [2- (4-Bromophenyl) -quinazolin-4-yl] - (5- methyl-2ff-pyrazol-3-yl) -amine (111-34) : mp 262-265°C; XH NMR (DMSO) δ 2.34 (3S, s) , 6.73 (IH, s) , 7.55 (IH, m) , 7.74 (2H, d),.7.83 (2H, m) , 8.40 (2H, d) , 8.65 (IH, d) , 10.44 (IH, s) , 12.25 (IH, a)'; IR (solid) 1603, 1579, 1546, 1484, 1408, 1365; MS 380.1/382.1 (M+H)+.
Example 263 [2- (4-Chlorophenyl) -quinazolin-4-yl] - (5- methyl-2ff-pyrazol-3-yl) -amine (111-35) : mp >300°C; XH NMR (DMSO) δ 2.34 (3H, s) , 6.74 (IH, s) , 7.53-7.62 (3H, m) , 7.84 (2H, d) , 8.47 (2H, d) , 8.65 (IH, d) , 10.44 (IH, s) , 12,26 (IH, s) ; IR (solid) 1628, 1608, 1584, 1546, 1489, 1408, 1369, 1169; MS 336.2 (M+H) + .
Example 264 [2- (3, 5-Dichlorophenyl) -quinazolin-4-yl] - (5- methyl-2ff-pyrazol-3-yl) -amine (111-36) : mp 228°C; XH NMR (DMSO) δ 2.34 (3H, s) , 6.69 (IH, s) , 7.96 (IH, d) , 8.21 (3H, m) , 8.56 (IH, d) , 8.60 (2H, d) , 10.51 (IH, s) , 12.30 (IH, s) ; IR (solid) 1546, 1331, 802, 763, 729, 658, 652; MS 370.5 (M+H)+.
Example 265 [2- (4-Cyanophenyl) -quinazolin-4-yl] - (5- methyl-2ff-pyrazol-3-yl) -amine (111-37) : mp 263°C; XH NMR (DMSO) δ 2.34 (3H, s) , 6.72 (IH, s) , 7.61 (IH, d) , 7.88 (2H, s) , 8.04 (2H, d) , 8.63 (2H, d) , 8.67 (IH, s) , 10.52 (IH, s) , .12.27 (IH, s) ; IR (solid) 1739, 1436, 1366, 1229, 1217; MS 327.2 (M+H)+.
Example 266 [2- (3-Iodophenyl) -quinazolin-4-yl] - (5-methyl- 2ff-pyrazol-3-yl) -amine (111-38) : mp 234-235°C; XH NMR (DMSO) δ 2.35 (3H, s) , 6.73 (IH, s) , 7.35 (IH, m) , 7.56 (IH, m) , 7.85 (3H, m) , 8.47 (IH, m) , 8.65 (IH, m) , 8.86 (IH, s) , 10.49 (IH, s) , 12.28 (IH, br s) ; IR (solid) 1560, 1541, 1469, 1360; MS 428.1 (M+H)+.
Example 267 [2- (4-Ethylsulfanylphenyl) -quinazolin-4-yl] - (5-methyl-2ff-pyrazol-3-yl) -amine (111-39) : mp 229-231°C; XH NMR (DMSO) δ 1.29 (3H, t) , 2.35 (3H, s) , 3.07 (2H, q) , 6.76 (IH, s) , 7.43 (2H, d) , 7.51 (IH, m) , 7.81 (2H, m) , 8.41 (2H, d) , 8.64 (IH, d) , 10.38 (IH, s) , 12.24 (IH, br s) ; IR (solid) 1587, 1574, 1555, 1531, 1484, 1412, 1369; MS 362.1 (M+H)+. Example 268 (5-Cyclopropyl-2ff-pyrazol-3-yl) - (2-phenyl- quinazolin-4-yl) -amine (III-4Q) : mp 218-219°C; XH NMR
(DMSO-d6) δ 0.70-0.80(2H, m) , 0.90-1.00 (2H, m) , 6.70
(IH, s) , 7.45-7.55 (4H, m) / 7.80-7.85 (2H, m) , 8.45-8.55 (2H, ) , 8.65 (IH, d) , 10.40 (IH, s) , 12.27 (IH, s) ; IR
(solid) 1624, 1605, 1591, 1572, 1561, 1533, 1479, 1439, 1419, 1361, 1327, 997, 828, 803, 780, 762, 710; MS 328.2
(M+H) + .
Example 269 [2- (4-tert-Butylphenyl) -quinazolin-4-yl] - (5- methyl-2ff-pyrazol-3-yl) -amine (111-41) : mp >300°C; XH NMR (DMSO-d6) δ 1.35 (9H, s) , 2.34 (3H, s) , 6.79 (IH, s) , 7.55 (3H, d) , 7.85 (2H, d) , 8.39 (2H, d) , 8.62 (IH, d) , 10.35 (IH, s) , 12.22 (IH, s) ; IR (solid) 1603, 1599, 1577, 1561, 1535, 1481, 1409, 1371, 1359, 998, 841, 825, 766, 757; MS 358.3 (M+H) + .
Example 270 [2- (4-Chlorophenyl) -quinazolin-4-yl] - (5- cyclopropyl-2ff-pyrazol-3-yl) -amine (111-42) : XH NMR (DMSO- d6) δ 0.77 (4H, br m) ,2.05 (IH, m) , 6.59 (IH, s) , 7.60 (IH, d) , 7.85 (2H, d) , 7.91 (2H, d) , 8.22 (2H, d) , 8.65 (IH, s) , 10.51 (lH,s), 12.33 (lH,s); MS 362.1 (M+H)+.
Example 271 (2-Benzo [1, 3] dioxol-5-yl-quinazolin-4-yl) - (5- methyl-2ff-pyrazol-3 -yl) -amine (111-43) : XH NMR (DMSO) δ 2.33 (3H, s) , 6.13 (2H, s) , 6.78 (lH,s), 7.11 (IH, d) , 7.80 (IH, t) , 7.94 (IH, s) , 8.09 (3H, m) , 8.25 (IH, d) , 10.34 (IH, s) , 12.21 (IH, s) ; MS 346.5 (M+H)+.
Example 272 [2- (4-Dimethylaminophenyl) -quinazolin-4-yl] - (5-methyl-2ff-pyrazol-3-yl) -amine (111-44) : XH NMR (DMSO- d6) δ 2.02 (6H, s) , 2.39 (3H, s) , 6.83 (IH, s) , 7.71 (IH, d) , 7.98 (2H, s) , 8,04 (2H, d) , 8.33 (2H, d) , 8.67 (IH, s) , 11.82 (IH, s) , 12.72 (IH, s) ; MS 345.3 (M+H)+.
Example 273 [2- (3-Methoxyphenyl) -quinazolin-4-yl] - (5- methyl-2ff-pyrazol-3-yl) -amine (111-45) : mp 226°C; XH NMR (DMSO) δ 2.34 (3H,s), 3.92 (3H, s) , 6.72 (IH, s) , 7.21 (IH, d) , 7.57 (IH, t) , 7.79 (IH, t) , 8.02 (3H, m) , 8.14 (IH, S) , 8.79 (IH, d) , 10.39 (lH,s), 12.22 (IH, s) ; IR (solid) 1599, 1572, 1538, 1478, 1427, 1359, 833, 761, 661; MS 332.2 (M+H)+.
Example 275 (5-Cyclopropyl-2ff-pyrazol-3-yl) - [2- (3,4- dichlorophenyl) -quinazolin-4-yl] -amine (111-46) : XH NMR (DMSO-d6) δ 0.86 (2H, d) , 1.02 (2H, d) , 1.69 (IH, m) , 6.56 (IH, s) , 7.57 (IH, d) , 7.84 (4H, m) , 8.40 (IH, d) ,
8.58 (IH, s) , 8.64 (IH, s) , 10.53 (IH, s) , 12.36 (IH, s) ; MS 396.0 (M+H)+.
Example 276 (2-Biphenyl-4-yl-quinazolin-4-yl) - (5-methyl- 2ff-pyrazol-3-yl) -amine (111-47) : .To a mixture of [2- (4- bromo-phenyl) -quinazolin-4-yl] - (5-methyl-2ff-pyrazol-3- yl) -amine (111-34) (196 mg, 0.51 mmol) and phenylboronic acid (75 mg, 0.62 mmol) in THF:water (1:1, 4 mL) was added Na2C03 (219 mg, 2.06 mmol), triphenylphosphine (9mg, 1/15 mol%) and palladium acetate (1 mg, 1:135 mol%) . The resulting mixture was heated at 80°C overnight, the solvents were evaporated and the residue purified by flash chromatography (gradient of dichloromethane:MeOH) to afford 111-21 as a yellow solid ( 99 mg, 51%) : XH NMR (DMSO) δ 2.37 (3H, s) , 6.82 (IH, s) , 7.39-7.57 (4H, ) ,
7.73-7.87 (6H, m) , 8.57 (2H, d) , 8.67 (IH, d) , 10.42 (IH, s) , 12.27 (IH, s) ; MS 378.2 (M+H)+. Example 277 [2- (4-Ethynylphenyl) -quinazolin-4-yl] - (5- methyl-2ff-pyrazol-3-yl) -amine (111-48) : To a mixture of [2- (4-bromo-phenyl) -quinazolin-4-yl] - (5-methyl-2ff- pyrazol-3-yl) -amine (111-34) (114 mg, 0.3 mmol), and trimethylsilylacetylene (147 mg, 1.5 mmol) in DMF (2 mL) was added Cul (1.1 mg, 1:50 mol%) , Pd(PPh3)2Cl2 (4.2 mg, 1:50 mol%) and triethylamine (121 mg, 0.36 mmol). The resulting mixture was heated at 120°C overnight and the solvent evaporated. The residue was triturated in ethyl acetate and the resulting precipitate collected by filtration. The collected solid was' suspended in THF (3 mL) and TBAF (IM in THF, 1. leq) was added. The reaction mixture was stirred at room temperature for 2 hours and the solvent evaporated. The residue was purified by flash chromatography (silica gel, gradient of DCM:MeOH) to afford 111-48 as a white solid (68 mg, 70%) -. XH NMR (DMSO) δ 2.34 (3H, s) , 4.36 (IH, s) , 6.74 (IH, s) , 7.55 (IH, m) , 7.65 (2H, d) , 7.84 (2H, m) , 8.47 (2H,. d) , 8.65 (IH, d) , 10.43 (IH, s) , 12.24 (IH, s) ; MS 326.1 (M+H)+.
Example 278 [2- (3-Ethynylphenyl) -quinazolin-4-yl] - (5- methyl-2ff-pyrazol-3-yl) -amine (111-49) : mp 204-207°C; XH NMR (DMSO) δ 2.34 (3H, s) , 4.28 (IH, s) , 6.74 (IH, s) , 7.55-7.63 (3H, m) , 7.83-7.87 (2H, m) , 8.49 (IH, d) , 8.57 (IH, s) , 8.65 (IH, d) , 10.46 (IH, s) , 12.27 (IH, s) ; IR (solid) .1598, 1574, 1541, 1489, 1474, 1422, 1365; MS 326.1 (M+H)+.
Example 279 [2- (3-Methylphenyl) -quinazolin-4-yl] - (5- methyl-2ff-pyrazol-3-yl) -amine (111-50) -. A suspension of lff-quinazoline-2,4-dione (10.0 g, 61.7 mmol) in P0C13 (60 mL, 644 mmol) and N,N-dimethylaniline (8mL, 63.1 mmol) was heated under reflux for 2 h. The excess POCl3 was removed in vacuo, the residue poured into ice, and the resulting precipitate collected by filtration. The crude solid product 2, 4-dichloro-quinazoline (6.5 g, 53% yield) was washed with water and dried under vacuum for next step use without further purification. To a solution of the 2, 4-dichloro-quinazoline (3.3 g, 16.6 mmol) in anhydrous ethanol (150 mL) was added 5-methyl-Iff- yrazol- 3-yl amine (3.2 g, 32.9 mmol) and the resulting mixture was stirred at room temperature for 4 hours . The resulting precipitate was collected by filtration, washed with ethanol, and dried under vacuum to afford 4.0 g (93% yield) of (2-chloro-quinazolin-4-yl) - (5-methyl-lff- pyrazol-3-yl) -amine which was used in the next step without further purification. To a solution of the (2- chloro-quinazolin-4-yl) - (5-methyl-lff-pyrazol-3-yl) -amine (50 mg, 0.19 mmol) in DMF (1.0 mL) was added m-tolyl boronic acid (0.38 mmol), 2M NaC03 (0.96 mmol), and tri- t-butylphosphine (0.19 mmol). The flask was flushed with nitrogen and the catalyst. PdCl2(dppf) (0.011 mmol) added in one portion. The reaction mixture was then heated at 80 °C for 10 hours, cooled to room temperature, and poured into water (2 mL) . The resulting precipitate was collected by filtration, washed with water, and purified by HPLC to afford 111-50 as a pale yellow solid (61mg, 75%): XH NMR (500 MHz, DMSO-d6) δ 12.3 (br s, IH) , 10.4 (br s, IH) , 8.75 (d, IH) , 8.30 (s, IH) , 8.25 (d, IH) , 7.78 (s, 2H) , 7.55 (m, IH) , 7.45 (m, IH) , 7.35 (m, IH) , 6.80 (s, IH) , 2.47 (s, 3H) , 2.30 (s, 3H) ; MS 316.1. (M+H).
Example 280 [2- (3 , 5-Dif luorophenyl) -quinazolin-4 -yl] - (5 - methyl-2ff-pyrazol-3 -yl) -amine (111-51) : XH NMR ( 500 MHz , DMS0-d6) δ l2 .3 (br s , IH) , 10 . 8 (br s, IH) , 8 . 63 (d, IH) , 7.95 (d, 2H) , 7.85 ( , 2H) , 7.58 (t, IH) , 7.41 (t, IH) , 6.59 (s, IH) , 2.27 (s, 3H) ; MS 338.1 (M+H) .
Example 281 [2- (3 -Chloro-4- fluorophenyl) -quinazolin-4- yl] -(5-methyl-2ff-pyrazol-3-yl) -amine (111-52) : XH NMR (500 MHz, DMSO-d6) δl2.4 (br s, IH) , 10.8 (br s, IH) , 8.65 (d, IH) , 8.50 (d, IH) , 8.36 (m, IH) , 7.85 (m, IH) , 7.60 ( , IH) , 6.62 (s, IH) , 2.30 (s, 3H) ; MS 354.1 (M+H) .
Example 282 (5-Methyl-2ff-pyrazol-3-yl) - [2- (3- trif luoromethylphenyl) -quinazolin-4-yl] -amine (111-53) : XH
NMR (500 MHz, DMSO-d6) δ 12.2 (br, IH) , 10.45 (br, IH) , 7.53 (s, IH) , 7.43 (d, J = 7.2 Hz, IH) , 7.06 (d, J = 8.2 Hz, IH) , 6.65 (d, J = 8.3 Hz, IH) , 6.57 (t, J = 7.6 Hz, IH) , 6.51 (d, J = 7.8 Hz, IH) , 6.43 (t, J = 7.8 Hz, IH) , 6.32 (t, J = 7.6 Hz, IH) , 5.51 (s, IH) , 2.03 (s, 3H) ; MS 370.2 (M+H) .
Example 283 [2- ( 3 - Cyanopheny 1 ) -quinazolin-4-yl] - (5- methyl -2ff-pyrazol- 3 -yl) -amine (111-54) : XH NMR (500 MHz, DMSO-d6) 69.01 (s, IH) , 8.96 (m, 2H) , 8.28 (d, J = 7.3 Hz, IH) , 8.16 (s, br, 2H) , 8.06 (t, J = 7.8 Hz, IH) , 7.88 (m, IH) , 6.96 (S, IH) , 2.58 (s, 3H) ; MS 327.1 (M+H) .
Example 284 [2- (3-Isopropylphenyl) -quinazolin-4-yl] - (5- methyl-2ff-pyrazol-3-yl) -amine (111-55) : XH NMR (500 MHz, DMSO-d6) δ8.89 (d, J = 7.5 Hz, IH) , 8.37 (s, IH)', 8.26 (s, IH) , 8.08 ( , 2H) , 7.81 (t, br, IH) , 7.67 (m, 2H) , 6.88 (s, IH) , 3.12 ( , IH) , 2.40 (s, 3H) , 1.38 (d, J = 6.9 Hz, 6H) ; MS 344.2 (M+H) .
Example 285 (5-Methyl-2ff-pyrazol-3-yl) - (2-pyridin-3-yl- quinazol in -4-yl) -amine (111-56) : XH NMR (500 MHz, DMSO-d6) δ9.50 (s, IH) , 8.84 (d, J = 7.3 Hz, IH) , 8.80 (d, J = 4.4 Hz, IH) , 8.66 (d, J = 8.2 Hz, IH) , 7.87 (m, 2H) , 7.77 (m, IH) , 7.60 (t, J = 7.2 Hz, IH) , 6.67 (s, IH) , 2.28 (s, 3H) ; MS 303.1 (M+H) .
Example 286 [2- (3-Acetylphenyl) -quinazolin-4-yl] - (5- methyl-2ff-pyrazol-3-yl) -amine (111-57) : XH NMR (500 MHz, DMSO-d6) δ8.80 (s, IH) , 8.55 (d, J = 7.7 Hz, IH) , 8.42 (d, J = 7.6 Hz, IH) , 8.00 (d, J = 7.0 Hz, IH) , 7.76 (m, 2H) , 7.58 (t, J = 7.7 Hz, IH) , 7.48 (s, br, IH) , 6.60 (s, IH) , 2.49 (s, 3H) , 2.03 (s, 3H) ; MS 344.1 (M+H).
Example 287 [2- (3, 5-Ditrifluoromethylphenyl) -quinazolin- 4-yl] -(5-methyl-2ff-pyrazol-3-yl) -amine (111-58) -. XH NMR (500 MHz, DMSO-d6) δlθ.7 (s, br, IH) , 8.95 (s, 2H) , .8.63 (d, J = 8.2 Hz, IH) , 8.25 (s, IH) , 7.86 (m, 2H) , 7.58 (t, J = 6.9 Hz, IH) , 6.62 (s, IH) , 2.26 (s, 3H) ; MS 438.1 (M+H) .
Example 288 [2- (3-Hydroxymethylphenyl) -quinazolin-4-yl] - (5-methyl-2ff-pyrazol-3 -yl) -amine (111-59) : XH NMR (500 MHz, DMSO-d6) δ 8.74 (d, J = 7.9 Hz, IH) , 8.33 (s, IH) , 8.17 (s, br, IH) , 7.95 (s, br, IH) , 7.89 (s, br, IH) , 7.62 (m, 3H) , 6.72 (s, IH) , 5.53 (s, IH) , 4.60 (s, 2H) , 2.28 (s, 3H) ; MS 332.1 (M+H).
Example 289 (5-Methyl-2ff-pyrazol-3-yl) - [2- (3- phenoxyphenyl) -quinazolin-4-yl] -amine (111-60) : mp 231- 232°C; XH NMR (DMSO-d6) δ 2.21 (3H, s) , 6.59 (IH, s) , 7.10-7.22 (4H, m) , 7.41-7.45 (2H, m) , 7.54-7.59 (2H, m) , 7.81 (2H, s) , 8.09 (IH, s) , 8.27 (IH, m) , 8.64 (IH, m) , 10.40 (IH, s)', 12.20 (IH, s) ; IR (solid); IR (solid) 1589, 1560, 1541, 1536, 1484, 1360, 1227; MS 394.7 (M+H)+. Example 290 (5-Cyclopropyl-2ff~pyrazol-3-yl) - [2- (3- phenoxypheny1) -quinazolin-4-yl] -amine (111-61) : mp 193- 195°C; XH NMR (DMS0-d6) 6 0.67 (2H, m) , 0.93 (2H, m),1.87
(lH,m) , 6.56 (IH, s) , 7.06-7.20 (4H, m) , 7.40-7.43 (2H, m) , 7.55-7.59 (2H, m) , 7.81 (2H, s) , 8.11 (IH, s) , 8.27 (IH, m) , 8.63 (IH, m) , 10.43 (IH, s) , 12.26 (IH, s) ; IR
(solid); IR (solid) 1589, 1574, 1527, 1483, 1369, 1226; MS 420.7 (M+H)+.
Example 291 (5-Methyl-2ff-pyrazol-3-yl) - (2-thiophen-3-yl- quinazolin-4-yl) -amine (IIΪ-62) : XH NMR (500 MHz, DMSO-d6) δll.78 (s, br, IH) , 8.75 (d, J = 8.1 Hz, IH) , 8.68 (s, IH) , 7.98 (dd, J = 7.9, 7.5 Hz, IH) , 7.89 (m, 2H), 7.81 (m, IH) , 7.68 (t, J = 7.5 Hz, IH) , 6.69 (s, IH) , 2.30 (s, 3H) ; MS 308.1 (M+H) .
Example 292 (2-Phenyl-quinazolin-4-yl) - (2ff-pyrazol-3-yl) - amine (111-63) : mp 247-249°C; XH NMR (DMSO) δ 6.99 (IH, br s) , 7.49-7.58 (5H, m) , 7.81 (IH, br s) , 7.83 (2H, m) , 8.47-8.49 (2H, ) , 8.66 (IH, d) , 10.54 (IH, s) , 12.59
(IH, S) ; IR (solid) 3145, 2922, 1622, 1597; MS 288.2
(M+H) + .
Example 293 (2ff-Pyrazol-3-yl) - (2-pyridin-4-yl-quinazolin- 4-yl)-amine (III-64):.mp 285-286°C; XH NMR (DMSO) δ 6.99 (IH, br s) , 7.65 (IH, m) , 7.81-7.94 (3H, m) , 8.3-8.35 (2H, m) , 8.73 (IH, d) , 8.84-8.90 (2H, m) , 10.76 (IH, s) , 12.6 (IH, s) ; IR (solid) 3180, 2972, 1600, 1574; MS 289.2 (M+H)+.
Example 294 5-Ethyl-2ff-pyrazol-3-yl) - (2 -phenyl - quinazolin-4 -yl) -amine (111-65 ) : mp 221-222 °C; XH NMR (DMSO) δ 1.31 (3H, t) , 2.68 (2H, d) , 6.80 (IH, s) , 7.50- 7.60 (4H, m) , 8.45-8.55 (2H, m) , 8.65-8.75 (IH, m) , 10.44 (lH,s), 12.27 (lH,s); IR (solid) 3190, 1622, 1595, 1575, 1533, 1482, 1441, 1420, 1403, 1361, 758, 711; MS 316.2 (M+H)+.
Example 295 (2-Phenyl-quinazolin-4-yl) - (5-propyl-2ff- pyrazol-3-yl) -amine (111-66) : mp 204-205°C; XH NMR (DMSO- d6) δ 1.02 (3H, t) , 1.66-1.75 (2H, m) , 2.69 (2H, t) , 6.80 (IH, S) , 7.45-7.60 (4H,m) ,• 7.80-7.88 (2H, m) , 8.45-8.50 (2H, m) , 8.65 (IH, d) , 10.39 (IH, s) , 12.25 (IH, s) ; IR (solid) 1621, 1560, 1572, 1533, 1479, 1441, 1421, 1363, 1328, 999, 827, 808, 763, 709, 697; MS 330.2 (M+H)+.
Example 296 (5-Isopropyl-2ff-pyrazol-3-yl) - (2-phenyl- quinazolin-4-yl) -amine (111-67) : mp 218-219°C; XH NMR (DMSO-d6) δ 1.36 (6H, d) , 3.05 (IH, m) , 6.86 (IH, s) , 7.48-7.59 (4H, m) , 7.80-7.88 (2H, m) , 8.49-8.58 (2H, m) , 8.66 (IH, d) , 10.47 (IH, s) , 12.30 (IH, s) ; IR (solid) 3173, 2968, 1619, 1593, 1573, 1533, 1478, 1438, 1413,
1398, 1363, 1329, 995, 822, 798, 761, 707, 666, 659; MS 330.2 (M+H)+.
Example 297 (5-tert-Butyl-2ff-pyrazol-3-yl) - (2-phenyl- quinazolin-4-yl) -amine (111-68) : mp 136-137°C; XH NMR
(DMS0-d6) δ 1.38 (9H, s) , 6.87 (IH, br s) , 7.51-7.57 (4H, m) , 7.84-7.85 (2H, m) , 8.49-8.51 (2H, m) , 8.65 (IH, d) , 10.43 (IH, s) , 12.21 (IH, br s) ; IR (solid) 3162, 2963, 1621, 1590, 1572; MS "344.2 (M+H) +.
Example 298 (5 -tert-Butyl-2ff-pyrazol-3 -yl) - (2 -pyridin-4 - yl-quinazolin-4 -yl) -amine (111- 69) : mp >300°C; XH NMR (DMSO) δ 1 . 38 ( 9H, s ) , 6 . 82 ( IH, br s ) , 7 . 63 ( IH, m) , 7.86-7.91 (2H, m) , 8.32-8.33 (2H, d) , 8.69 (IH, d) , 8.75-8.76 (2H, d) , 10.60 (IH, s) , 12.31 (IH, br s) ; IR (solid) 3683, 3149, 2963, 1621; MS 345.2 (M+H)+.
Example 299 (5-Cyclopentyl-2ff-pyrazol-3-yl) - (2-phenyl- quinazolin-4-yl) -amine (111-70) : mp 240-241°C; XH NMR (DMSO-d6) δ 1.68-1.89 (6H, ) , 2.03-2.17 (2H, m) , 3.14- 3.22 (IH, m) , 6.80 (IH, s) , 7.50-7.60 (4H, m) , 7.80-7.89 (2H, ) , 8.45-8.52 (2H, m) , 8.67 (IH, d) , 10.52 (IH, s) , 12.26 (IH, s) ; IR (solid) 2957, 1621, 1591, 1571, 1531, 1476, 1438, 1405, 1370, 1325, 999, 951, 801, 775, 761, 747, 710695, 668, 654; MS 356.2(M+H)+.
Example 300 (5-Phenyl-2ff-pyrazol-3-yl) - (2-phenyl- quinazolin-4-yl) -amine (111-71) : mp 207-209°C; XH NMR
(DMSO) δ 7.38-7.40 (IH, m) , 7.50-7.58 (6H, m) , 7.82-7.88 (4H, m) , 8.51 (2H, m) , 8.67 (IH, s) , 10.58 (IH, s) , 13.11 (IH, br s) ; IR (solid) 3345, 3108, 1627, 1612; MS 364.2 (M+H)+.
Example 301 (5-Carboxy-2ff-pyrazol-3-yl) - (2-phenyl- quinazolin-4-yl) -amine (111-72) : (5-Methoxycarbonyl-2ff- pyrazol-3-yl) - (2-phenyl-quinazolin-4-yl) -amine (III-73) (345mg, 1 mmole in THF, 6 mL) was treated with NaOH (IM, 4.0 mL) , stirred at 50°C for 5 hours, cooled to room temperature, and neutralised with IM HCl . The mixture was concentrated in vacuo to remove THF then diluted with water and the resulting precipitate filtered. The residual solid was dried at 80°C under vacuum to afford 111-72 as an off-white solid (312 g, 94%) : mp 289-291°C (dec); XH NMR (DMSO) δ 7.45 (IH, br s) , 7.50-7.60 (5H, m) , 7.80-7.88 (2H, m) , 7.40-7.50 (2H, m) , 8.60-8.70 (IH, d) , 10.70 (IH, s) , 13.00-13.80 (2H, br s) ; IR (solid) 1699, 1624, 1607, 1570,1539, 1506, 1486, 1398, 1333, 1256, 1177, 1004, 827, 764, 705; MS 332.3 (M+H)+.
Example 302 (5-Methoxycarbonyl-2ff-pyrazol-3-yl) - (2- phenyl-quinazolin-4-yl) -amine (111-73) : mp 271-273°C; XH NMR (DMSO) .δ 3.95 (3H, s) , 7.50-7.65 (5H, m) , 7.80-7.98 (2H, ) , 8.40-8.50 (2H, m) , 8.65-8.73 (IH, ) , 10.80 (IH, s) , 13.80 (IH, S) ; IR (solid) 3359, 1720, 1624, 1597, 1561, 1538, 1500, 1475, 1435, 1410, 1358, 1329, 1283, 1261, 1146, 1125, 1018, 1010, 944, 827, 806, 780, 763, 703, 690, 670; MS 346.3 (M+H)+.
Example 303 (5-Hydroxymethyl-2ff-pyrazol-3-yl) - (2-phenyl- quinazolin-4-yl) -amine (111-74) : A solution of (5- Methoxycarbonyl-2ff-pyrazol-3-yl) - (2-phenyl-quinazolin-4- yl) -amine (111-73) (345mg, lmmol) in anhydrous THF (lO L) was treated with lithium borohydride (125mg, 5.75 mmol) at 65°C for 5 hours . The mixture was cooled to room temperature then combined with 2M HCl and ethyl acetate. Solid sodium hydrogen carbonate was added to achieve pH 8 and the resulting mixture extracted with ethyl acetate. The extracts were dried over magnesium sulphate and concentrated. Purification by flash chromatography (Si02, methanol-dichloromethane gradient) afforded III-74 (95 mg, 30%) as an off-white solid: mp 238-239°C; XH NMR
(DMSO) δ 4.58 (2H, d, CH2) , 5.35 (IH, s, OH), 6.94 (IH, s) , 7.50-7.60 (4H, m) , 7.85-7.90 (2H, m) , 8.48-8.54 (2H, m) , 8.69 (IH, IH) , 10.40 (IH, s) , 12.48 (IH, s) ; IR (solid) 1652, 1621, 1603, 1575, 1558, 1539, 1532, 1480, 1373, 1320, 1276, 1175, 1057, 1037, 1007, 951, 865, 843, 793, 780, 7124; MS 318.2 (M+H)+. Example 304 (5-Methoxymethyl-2ff-pyrazol-3-yl) - (2-phenyl- quinazolin-4-yl) -amine (111-75) : mp 190-191°C; XH NMR (DMSO) δ 3.34 (3H, s) , 4.45 (2H, s) , 7.00 (IH, s) , 7.50-
7.62 (4H, m) , 7.82-7.90 (2H, m) , 8.45-8.52 (2H, m) , 8.65 (IH, br s) , 10.50 (IH, s) , 12.30 (IH, s) ; IR (solid)
3177, 1606, 1589, 1530, 1479, 1441, 1406, 1374, 1363, 1329, 1152, 1099, 999, 954, 834, 813, 766,. 707, 691; MS 332.3(M+H)+.
Example 305 [5- (3-Hydroxyprop-l-yl) -2ff-pyrazol-3-yl] - (2- phenyl-quinazolin-4-yl) -amine (111-76) : A solution of (5- benzyloxypropyl-2ff-pyrazol-3-yl) - (2-phenyl-quinazolin-4- yl) -amine (111-78) (200mg, 0.46mmol) in toluene (4mL) and acetonitrile (8mL) was stirred with trimethylsilyl iodide (0.64ml, 4.6mmol) at 55°C for 3 hours to afford an amber coloured solution. This mixture was diluted with ethyl acetate and aqueous sodium hydrogen carbonate.. The resulting layers were separated, the organic layer was dried over magnesium sulphate and concentrated in vacuo. Purification by flash chromatography (Si02, methanol- dichloromethane gradient) affords a yellow oil (115mg) . Trituration with dichloromethane affords III-76 as an off-white solid dried at 75°C under vacuum (83mg, 52%) : mp 164-165°C; XH NMR (DMSO) δ 1.80-1.90 (2H, m) , 2.70-2.80 (2H, m) , 3.50-3.60 (2H, m) , 4.59 (IH, s) , 6.80 (IH, s) , 7.50-7.60 (4H, m) , 7.82-7.90 (2H, m) , 8.48-8.53 (2H, m) ,
8.63 (IH, s) , 10.40 (IH, s) , 12.25 (IH, s) ; IR (solid) 1622, 1587, 1574, 1562, 1528, 1480, 1440, 1421, 1368, 1329, 1173, 1052, 1030, 1006, 952, 833, 762, 734, 706, 690, 671, 665; MS 346.0(M+H)+.
Example 306 [5- (3 -Me hoxyprop-l-yl) -2ff-pyrazol-3-yl] - (2- phenyl-quinazolin-4 -yl) -amine (111-77) : mp 169-170 °C; XH NMR (DMSO-d6) δ 1.86-1.97 (2H, m) , 2.75 (2H, t) , 3.30 (3H, s) , 3.45 (2H, t) , 6.80 (IH, s) , 7.50-7.60 (4H, m) , 7.80- 7.90 (2H, m) , 8.45-8.55 (2H, m) , 8.67 (IH, d) , 10.30 (IH, s) , 12.25 (IH, s) ; IR (solid) 1620, 1591, 1572, 1532, 1476, 1425, 1408, 1373, 1326, 1117, 1003, 831, 764, 714, 695; MS 360.3 (M+H)+.
Example 307 [5- (3-Benzyloxyprop-l-yl) -2ff-pyrazol-3-yl] - (2-phenyl-quinazolin-4-yl) -amine (111-78) : mp 177-178°C; XH NMR (DMSO) δ 1.92-2.03 (2H, m) , 3.76-3.85 (2H, m) ,
3.52-3.62 , (2H, m) , 4.51 (2H, s) , 6.82 (IH, s) , 7.28-7.40 (5H, m) , 7.46-7/58 (4H, m) , 7.80-7.85 (2H, m) , 8.47-8.52 (2H, m) , 8.66 (IH, d) , 10.45 (IH, s) ; IR (solid) 1621, 1591, 1562, 1532, 1479, 1454, 1426, 1408, 1374, 1101, 1006, 835, 766, 738, 712, 696; MS 436.3 (M+H)+.
Example 308 [5- (3-Aminoprop-l-yl) -2ff-pyrazol-3-yl] - (2- phenyl-quinazolin-4-yl) -amine (111-79) : A solution of [5- (3-tert-butoxycarbonylaminoprop-l-yl) -2ff-pyrazol-3-yl] - (2-phenyl-quinazolin-4-yl) -amine (111-80) (250mg,
0.56mmol), in dichloromethane (3mL) at 0°C was treated with TFA (2mL) . The mixture was warmed to room temperature then concentrated in vacuo. The residue was triturated and concentrated from dichloromethane (3x5mL) and ether, then triturated with dichloromethane to crystallize the TFA salt. The resulting solid was collected by filtration and dissolved in a mixture of ethanol (3mL) and water (3mL) . ■ Potassium carbonate was added in portions to achieve pH 8 then the mixture allowed to crystallize. The product was collected by filtration and dried at 80°C under vacuum to afford III-79 as an off-white powder (122mg, 63%) : mp 205-207°C; XH NMR (DMSO) δ 1.68-1.83 (2H, m) , 2.65-2.80( 4H, m) , 6.80 (IH, s) , 7.50-7.60 (4H, ) , 7.80-7.90 (2H, ) , 8.45-8.53 (2H„ m) , 8.65 (IH, d) , 10.45 (IH, br s) ; IR (solid) 1621, 1598, 1568, 1533, 1484, 1414, 1364, 1327, 1169, 1030, 951, 830, 776, 764, 705, 677; MS 345.3 (M+H)+.
Example 309 [5- (3-tert-Butoxycarbonylaminoprop-l-yl) -2ff- pyrazol-3-yl] - (2-phenyl-quinazolin-4-yl) -amine (111-80) : mp 199-200°C; XH NMR (DMSO) δ 1.37 (9H, s) , 1.71-1.82 (2H,m) , 2.67 (2H, t) , 3.00-3.11 (2H, m) , 7.81 (IH, s) , 7.99 (IH, s) , 7.50-7.60 (4H, m) , 7.80-7.85 (2H, m) , 8.48- 8.52 (2H, m) , 8.63 (IH, d) , 10.40 (IH, s) , 12.26 (IH, m) ; IR (solid) 2953, 1687, 1622, 1594, 1573, 1535, 1481, 1441, 1419, 1364, 1327, 1281, 1252, 1166, 1070, 1028, 998, 951, 848, 807, 768, 740, 728, 710,693; MS 445.3 (M+H)+.
Example 310 5-lsopropylcarbamoyl-2ff-pyrazol-3-yl) - (2- phenyl-quinazolin-4-yl) -amine (111-81) : XH NMR (500MHz, DMS0-d6) δ 1.20 (d, J = 6.6 Hz, 6H) , 4.13 (m, IH) , 7.42 (br. s, IH) , 7.61 (dd, J.= 7.0, 7.7 Hz, 2H) , 7.66 (t, J = 7.1 Hz, IH) , 7.71 (m, IH) , 7.99 ( , 2H) , 8.39 (m, IH) , 8.42 (d, J = 7.1 Hz, 2H) , 8.74 (d, J = 8.2 Hz, IH) , 11.41 (br. s, IH) ; EI-MS 373.2 (M+H); HPLC-Method C, Rt 14.09 min.
Example 311 (5-Allylcarbamoyl-2ff-pyrazol-3-yl) - ( 2 -phenyl - quinazolin- 4-yl) -amine (111-82) : XH NMR (500MHz, DMSO-d6) δ 4.02 (m, 2H) , 5.15 (m, IH) , 5.23 (m, IH) , 5.94 (m, IH) , 7.45 (br. s, IH) , 7.60 (t, J = 6.9 Hz, 2H) , 7.64 (m, IH) , 7.72 (m, IH) , 7.98 (m, 2H) , 8.43 (m 2H) , 8.72 (d, J = 8.2 Hz, IH) , 8.84 (br. s, IH) , 11.34 (br. s, IH) ; EI-MS 371.2 (M+H); HPLC-Method C, Rt 13.67 min. Example 312 [5- (2-Methoxyethylcarbamoyl) -2ff-pyrazol-3- yl] - (2-phenyl-quinazolin-4-yl) -amine (111-83) •. XH NMR
(500MHz, DMSO-d6) δ 3.32 (s, 3H) , 3.48 (m, 4H) , 7.36 (br. s, IH) , 7.62 (m, 2H) , 7.63 (m, IH) , 7.71 (m, IH) , 7.98 (m, 2H) , 8.41 (dd, J = 1.4, 7.0, 2H) , 8.70 (m, 2H) , 11.30
(br. s, IH) ; EI-MS 389.2 (M+H); HPLC-Method C, Rt 12.37 min.
Example 313 (5-Benzylcarbamoyl-2ff-pyrazol-3-yl) - (2- phenyl-quinazolin-4-yl) -amine (111-84) : XH NMR (500MHz, DMSO-d6) δ 4.52 (d, J = 6.0 Hz, 2H) , 7.29 (m, IH) , 7.38 (d, J = 4.2 Hz, 4H) , 7.58 (t, J = 7.5 Hz, 2H) , 7.63 (m, IH) , 7.72 (m, IH) , 7.98 (m, 2H) , 8.43 (d, J = 7.7 Hz, 2H) , 8.72 (d, J = 7.5 Hz, IH) , 9.23 (br. s, 2H) , 11.34 (br. S, IH) ; EI-MS 421.2 (M+H); HPLC-Method C, Rt 16.76 min.
Example 314 (5-Cyclohexylcarbamoyl-2ff-pyrazol-3-yl) - (2- phenyl-quinazolin-4-yl) -amine (111-85) : XH NMR (500MHz, DMSO-d6) δ 1.16 (m, IH) , 1.34 (m, 4H) , 1.62 (d, J = 2.6 Hz, IH) , 1.76 ( , 2H) , 1.85 (m, 2H) , 3.79 (m, IH) , 7.43 (m, IH) , 7.60 (t, J = 7.2 Hz, 2H) , 7.65 (t, J = 7.1 Hz, IH) , 7.71 (ddd, J = 2.2, 5.4, 8.2 Hz, IH) , 7.98 (m, 2H) , 8.35 (m, IH) , 8.43 (dd, J = 1.4, 7.2 Hz, 2H) , 8.72 (d, J = 8.2 Hz, IH) , 11.34 (br. s, IH) ; EI-MS 413.5 (M+H); HPLC-Method C, Rt 17.18 min.
Example 315 (5-Diethylcarbamoyl-2ff-pyrazol-3-yl) - (2- phenyl- quinazolin- 4-yl) -amine (111-86) : XH NMR (500MHz, DMSO-d6) δ 1.18 (br. s, 3H) , 1.25 (br. s, 3H) , 3.49 (br. s, 2H) , 3.69 (b. S, 2H) , 7.21 (s, IH) , 7.59 (t, J = 6.9 Hz, 2H) , 7.62 (m, IH) , 7.70 (m, IH) , 7.96 (m, 2H) , 8.39 (d, J = 7.1 Hz, 2H) , 8.74 (d, J = 8.4 Hz, IH) , 11.37 (br. s, IH) ; EI-MS 387.2 (M+H); HPLC-Method C, Rt 14.50 min.
Example 316 [5- (Benzyl-methyl-carbamoyl) -2ff-pyrazol-3- yl] - (2 -phenyl-quinazolin-4-yl) -amine (111-87) : XH NMR
(500MHz, DMSO-dβ) δ 3.33 (s, 3H) , 4.75 (s, 2H) , 7.26 (m, IH) , 7.31 (m, IH) , 7.38 ( , 4H) , 7.58 (m, 2H) , 7.70 (m, IH) , 7.95 (m, 3H) , 8.26 (m, IH) , 8.40 (d, J = 7.8 Hz, 2H) , 8.75 ( , IH) , 11.2 (br. s, IH) ; EI-MS 435.2 (M+H); HPLC-Method C, Rt 16.77 min.
Example 317 (2-Phenyl-quinazolin-4-yl) - (5- propylcarbamoyl-2ff-pyrazol-3-yl) -amine (111-88) : XH NMR (500MHz, DMSO-d6) δ 0.94 (t, J = 7.3 Hz, 3H) , 1.57 (m, 2H) , 3.24 (q, J = 6.5 Hz, 2H) , 7.39 (br. s, IH) , 7.60 (t, J = 7.3 Hz, 2H) , 7.64 (m, IH) , 7.71 (br. t, J = 6.5 Hz, IH) , 7.98 (m, 2H) , 8.42 (d, J = 7.2 Hz, 2H) , 8.61 (br. s, IH) , 8.72 (d, J = 8.5 Hz, IH) , 11.34 (br. s, IH) ; EI-MS 373.3 (M+H); HPLC-Method C, Rt 13.51 min.
Example 318 [5- (Ethyl-isopropyl-carbamoyl) -2ff-pyrazol-3- yl] - (2 -phenyl-quinazolin-4-yl) -amine (111-89) : XH NMR (500MHz, DMSO-d6) δ 0.92 (t, J = 7.4 Hz, 6H) , 1.52 (m,. 2H) , 1.59 (m, IH) , 3.79 (m, 2H) , 7.53 (br. s, IH) , 7.57 (t, J = 7.5 Hz, 2H) , 7.65 (t, J = 7.2 Hz, IH) , 7.71 (m,
IH) , 7.99 (m, 2H) , 8.23 (br. d, J = 8.8 Hz, IH) , 8.46 (d, J = 7.5 Hz, 2H) , 8.74 (d, J = 8.4 Hz, IH) , 11.34 (br. s, IH) ; EI-MS 401.2 (M+H) ; HPLC-Method C, Rt 15.51 min.
Example 319 (5-Cyclopropylcarbamoyl-2ff-pyrazol-3-yl) - (2- phenyl- quinazolin- 4-yl) -amine (111-90) : XH NMR (500MHz, DMSO-d6) δ 0.60 (m, 2H) , 0.74 (m, 2H) , 2.86 (m, IH) , 7.34 (br. s, IH) , 7.62 (m, 3H) , 7.70 (m, IH) , 7.97 (m, 2H) , 8.41 (d, J = 7.9 Hz, 2H) , 8.63 (br. s, IH) , 8.72 (d, J = 7.8 Hz, IH) , 11.35 (br. s, IH) ; EI-MS 371.2 (M+H); HPLC- Method C, Rt 12.64 min.
Example' 320 (5-Isobutylcarbamoyl-2ff-pyrazσl-3-yl) - (2- phenyl-quinazolin-4-yl) -amine (111-91) : XH NMR (500MHz, DMSO-d6) δ 0.94 (d, J = 6.7 Hz, 6H) , 1.88 (m, IH) , 3.12 (t, J = 6.4 Hz, 2H) , 7.45 (br. s, IH) , 7.58 (t, J = 7.2 Hz, 3H) , 7.64 (t, J = 7.1 Hz, IH) , 7.71 (m, IH) , 7.98 ( , 2H) , 8.44 (dd, J = 1..3, 7.9 Hz, 2H) , 8.62 (br. s, IH) ,
8.72 (d, J = 8.3 Hz, IH) , 11.33 (br. s, IH) ; EI-MS 387.2 (M+H); HPLC-Method C, Rt 14.70 min.
Example 321 {5- [ (3S) -3-Methoxymethyl-pyrrσlidine-l- carbonyl] -2ff-pyrazol-3-yl}- (2-phenyl-quinazolin-4-yl) - amine (111-93) : XH NMR (500MHz, DMSO-d6) δ 2.00 ( , 2H) , 2.12 (m, IH) , 3.29 (s, 3H) , 3.45 (t, J = 8.7 Hz, IH) , 3.57 (dd, J = 3.2, 9.3 Hz, IH) , 3.86 (m, IH) , 3.92 (m, IH) , 4.36 (m, 2H) , 7.45 (br. s, IH) , 7.59 (t, J = 7.2 Hz, 2H) , 7.63 (m, IH) , 7.69 (m, 1H),.7.97 (m, 2H) , 8.40 (d, J = 7.5 Hz, 2H) , 8.74 (d, J = 7.6 Hz, IH) , 11.38 (br. s, IH) ; EI-MS 429.2 (M+H) ; HPLC-Method C, Rt 13.84 min.
Example 322 (2-Phenyl-quinazolin-4-yl) - (5-m- tolylcarbamoyl-2ff-pyrazol-3-yl) -amine (111-94) : XH NMR
(500MHz, DMSO-d6) δ 2.33 (s, 3H) , 6.97 (d, J = 7.5 Hz, IH) , 7.27 (t, J = 7.8 Hz, IH) , 7.62 (m, 7H) , 7.72 (m, IH) , 7.98 (m, 2H) , 8.46 (dd, J = 2.0, 7.9 Hz, 2H) , 8.71
(m, IH) , 10 . 29 ( s , IH) , 11 . 31 (br . s , IH) ; EI-MS 421 . 2 (M+H) ; HPLC-Method C, Rt 17 . 11 min .
Example 323 (2 -Phenyl-quinazolin-4 -yl) - (5-p- tolylcarbamoyl-2ff-pyrazol-3 -yl) -amine (111-95) : XH NMR (500MHz, DMSO-d6) δ 2.30 (s, 3H) , 7.20 (d, J = 8.3 Hz, 2H) , 7.62 (m, 5H) , 7.68 (d, J = 8.3 Hz, 2H) , 7.72 (m, IH) , 7.98 (m, 2H) , 8.46 (dd, J = 1.8, 7.0 Hz, 2H) , 8.72 (m, IH) , 10.31 (s, IH) , 11.36 (br. s, IH) ; EI-MS 421.2 (M+H) ; HPLC-Method C, Rt 16.95 min.
Example 324 (5-Methvlcarbamoyl-2ff-pvrazol-3-yl) - (2- phenyl-quinazolin-4-yl) -amine (111-96) : XH NMR (500MHz, DMSO-d6) δ 2.82 (d, J = 4.6 Hz, 3H) , 7.31 (br. s, IH) , 7.62 (m, 3H) , 7.69 (m, IH) , 7.97 (m, 2H) , 8.42 (d, J =
7.1 Hz, 2H) , 8.59 (br. s, IH) , 8.71 (d, J = 8.0 Hz, IH) , 11.30 (br. s, IH) ; EI-MS 345.1 (M+H); HPLC-Method C, Rt 11.02 min.
Example 325 [5- (Morpholine-4 -carbonyl) -2ff-pyrazol- 3 -yl] - (2-phenyl-quinazolin-4-yl) -amine (111-97) : XH NMR (500MHz, DMSO-d6) δ 3.33 (m, 4H) , 3.83 (m 4H) , 7.34 (br. s, IH) , 7.53 (m, 4H) , 7.86 (m, 2H) , 8.43 (m, 2H) , 8.67 (d, J = 8.6 Hz, IH) , 10.70 (s, IH) , 13.56 (s, IH) ; EI-MS 401.2 (M+H) ; HPLC-Method A, Rt 2.68 min.
Example 326 [5- (1-Methylpiperazine- 4 -carbonyl) -2ff- pyrazol-3-yl] - (2-phenyl-quinazolin-4-yl) -amine (111-98) :
XH NMR (500MHz, DMS0-d6) δ 2.25 (s, 3H) , 2.43 (m, 4H) , 3.87 (m 4H) , 7.33 (br. s, IH) , 7.53 (m, 4H) , 7.87 (m, 2H) , 8.45 (m, 2H) , 8.67 (d, >J, = 7.6 Hz, IH) , 10.70 (s, IH) , 13.30 (s, IH) ; EI-MS 414.2 (M+H) ; HPLC-Method A, Rt 2.38 mi .
Example 327 [5- (2-Hydroxyethylcarbamoyl-2H-pyrazol-3-yl] - (2-phenyl-quinazolin-4-yl) -amine (111-99) : XH NMR (500MHz, DMSO-d6) δ 3.36 (m, 2H) , 3.52 (m, 2H) , 4.79 (m, IH) , 7.50 (m, 5H) , 7.83 (m, 2H) , 8.50 (m, 4H) , 10.52 (br. s, IH) , 13.25 (s, IH) ; EI-MS 375.1 (M+H); HPLC-Method A, Rt 2.51 min.
Example 328 (5-Carbamoyl-2ff-pyrazol-3-yl) - (2-phenyl- quinazolin-4-yl) -amine (III-100): To a solution of 5- (2- phenyl-quinazolin-4-ylamino) -Iff-pyrazole-3 -carboxylic acid 2, 5-dioxo-pyrrolidin-l-yl ester (270 mg, 0.63 mmol) in DMF (20 ml) was added a solution of ammonia in 1,4- dioxane (0.5 M, 10 ml). The resulting mixture was stirred at room temperature for 24 h. After concentration of the solvents, the residue was added to water (20 ml) . The resulting precipitate was collected to afford III-100 (168 mg, 80%.) as a yellow solid. XH NMR (500MHz, DMS0-d6) δ 7.77-7.51 (m, 6H) , 7.86 (br s, 2H) , 8.11 (m, IH) , 8.50 (m, 2H) , 8.63 (m, IH) , 10.52 (s, IH) , 11.25 (s, IH) ; EI-MS 331.1 (M+H); HPLC-Method A, Rt 2.52' min.
Example 329 (4-Bromo-2ff-pyrazol-3-yl) - (2-phenyl- quinazolin-4-yl) -amine (III-101) : Prepared according to
Method A to afford a yellow solid, mp 189°C; XH NMR (DMSO- d6) δ 7.44-7.46 (3H, m) , 7.58 (IH, m) , 7.87 (2H, d) , 8.15 (IH, s) , 8.31-8.34 (2H, m) , 8.49 (IH, d) , 10.08 (IH, s) , 13.13 (IH, s) ; IR (solid) 3286, 2969, 1738, 1632; MS 366.2/368.2 (M+H)+.
Example 330 (4-Bromo-5-methyl-2ff-pyrazol-3-yl) - (2-phenyl- quinazolin-4-yl) -amine (III-102) : mp 183-185°C; XH NMR (DMSO) δ 2.33 (3H, br s) , 7.44-7.46 (3H, m) , 7.57 (IH, m) , 7.84-7.87 (2H, m) , 8.31-8.34 (2H, ) , 8.48 (IH, d) , 10.05 (IH, s) , 12.91 (IH, br s) ; IR (solid) 3362, 3065, 2831, 1619, 1578; MS 380.2/382.2 (M+H) +. Example 331 (4-Cyano-2ff-pyrazol-3-yl) - (2 -phenyl- quinazolin- -yl) -amine (III-103) : mp >250°C; XH NMR (DMSO) δ 7.47-7.49 (3H, m) , 7.64 (IH, m) , 7.91 (2H, m) , 8.40- 8.43 (2H, m) , 8.53 (IH, d) , 8.71 (IH, d) , 10.61 (IH, s) , 13.60 (IH, s) ; IR (solid) 3277, 3069, 2855, 2231, 1625; MS 313.2 (M+H) +. '
Example 332 (5-Methyl-2ff-pyrazol-3-yl) - (2-morpholin-4-yl- quinazolin-4-yl) -amine (III-104) : mp 223-224°C; XH NMR (DMSO) δ 2.26(3H, s) , 3.65 (4H, m) , 3.75(4H, m) , 6.4 (IH, s) , 7.12(1H, d) , 7.33(1H, d) , 7.56(1H, t) , 8.37(1H, d) , 10.0K1H, s) , 12.13(1H, br s) ; IR (solid) 1621, 1578, 1537, 1475, 1434, 1385; MS 311.0 (M+H)+.
■ Example 333 (5-Methyl-2ff-pyrazol-3-yl) - (2-piperazin-l-yl- quinazolin-4-yl) -amine (III-105) : mp 179-181°C; XH NMR (DMSO) δ 2.26 (3H, s) , 2.74 (4H, br s) , 3.71(4H, br s) , 6.43 (IH, s) , 7.08(1H, t) , 7.30(1H, d) , 7.53(1H, t) , 8.34 (IH, d) , 9.50 (IH, s) , 12.08 (IH, br s) ; IR (solid) 2853, 1619, 1603, 1566, 1549, 1539; MS 310.0 (M+H) +
Example 334 [2- (4-Methylpiperidin-l-yl) -quinazolin-4-yl] - (5-methyl-2ff-pyrazol-3 -yl) -amine (III-106) : mp 148-150°C; XH NMR (DMSO) δ 1.06(3H, d) , 1.03(2H, m) , 1.51-1.70 (3H, m) , 2.26(3H, s) , 2.86(2H, m) , 4.73(2H, • d) , 6.44(1H, s) , 7.06(1H, d) , 7.29(1H, d) , 7.52(1H, t) , 8.32(1H, d) , 9.92(1H, s) , 12.09(1H, br s) ; IR (solid) 2917, 2840, 1629, 1593, 1562, 1546, 1486; MS 323.0 (M+H)+.
Example 335 [2- (4-Methylpiperazin-l-yl) -quinazolin-4-yl] - (5-methyl-2ff-pyrazol-3-yl) -amine (III-107) : mp 105-107°C; XH NMR (DMSO) δ 2.21(3H, s) , 2.26(3H, s) , 2.34(4H, m) , 3.75(4H, m) , 6.45(1H, s) , 7.09(1H, t) , 7.31(1H, d) , 7.54 (IH, t) , 8.34(1H, d) , 9.96(1H, s) , 12.12 (IH, br s) ; IR (solid) 2934, 2844, 2804, 1620, 1593, 1572, 1536, 1476; MS 324.0 (M+H)+.
Example 336 (5-Methyl-2ff-pyrazol-3-yl) - (2-piperidin-l-yl- quinazolin-4-yl) -amine (III-108) : mp 294°C; XH NMR (DMSO) δ 1.45-1.58 (4H, m) , 1.63 (2H, ) , 2.26 (3H, s) , 3.79 (4H, m) , 6.45 (IH, br s) , 7.06 (IH, t) , 7.29 (IH, d) , 7.52 (IH, t) , 8.33 (IH, d) , 9.92 (IH, s) , 12.11 (IH, br s) ; IR (solid) 2929, 2847, 1632, 1591, 1500, 1482, 1437, 1382; MS 309.3 (M+H)+.
Example 337 (2-Azepan-l-yl) -quinazolin-4-yl] - (5-methyl- 2ff-pyrazol-3-yl) -amine (III-109) : mp 269°C; XH NMR (DMSO) δ 1.50 (4H, br s) , 1.76 (4H, br s), 2.25 (3H, s) , 3.78 (4H, t) , 6.55 (IH, br s) , 7.03 (IH, t) , 7.28 (IH, d) , 7.50 (IH, t) , 8.33 (IH, d) , 9.92 (IH, s) , 12.09 (IH, br S) ; IR (solid) 3427, 2963, 2927, 2909, 2872, 2850, 1623, 1595, 1586, 1568-, 1504, 1486, 1468, 1386, 1427; MS 323.3 (M+H)+.
Example 338 [2- (4- (2-Hydroxyethylpiperidin-l-yl) - quinazolin-4-yl] - (5-methyl-2ff-pyrazol-3-yl) -amine (III- 110): mp 175°C; XH NMR (DMSO) δ 1.08 (2H, m) , 1.38 (2H, m) , 1.57-1.83 (3H, m) , 2.26 (3H, s) , 2.85 (2H, t) , 3.47 (2H, m) , 4.38 (IH, t) , 4.75 (2H, d) , 6.45 (IH, br s) , 7.06 (IH, t) , 7.29 (IH, d) , 7.52 (IH, t) , 8.32 (IH, d) , 9.93 (IH, s) , 12.12 (IH, br s) ; IR (solid) 3365, 3073,. 2972, 2868, 1622, 1604, 1586, 1568, 1486, 1463, 1440, 1394; MS 353.2 (M+H)+.
Example 339 (5 -Cyclopropyl -2ff-pyrazol -3 -yl) - [2 - (4 - methylpiperidin-1-yl) -quinazolin-4 -yl] -amine (III- 111) : To a solution of (5-cyclopropyl-lH-pyrazol-3-yl) - (2- chloro-quinazolin-4-yl) -amine (118 mg, 0.41 mmol) in tert-butanol (3.0 mL) was added 4-methylpiperidine (0.49 mL, 4.1 mmol) and the reaction mixture heated at reflux overnight. The reaction mixture was concentrated in vacuo and the residue dissolved in a mixture EtOH: water (1:3,' 4 mL) . Potassium carbonate (57mg, 0.41 mmol) was added and the mixture stirred at room temperature for 2 hours. The resulting suspension was filtered, washed with water (x2) , and rinsed with Et20 (x2) to afford III- 111 as a white solid (123mg, 85%) : mp 190 °C; XH NMR (DMSO) δ 0.66 (2H, s) , 0.93. (5H, br s) , 1.07 (2H, d) , 1.66 (3H, s) , 1.91 (IH, s) , 2.85 (2H, t) , 4.72 (2H, d) , 6.33 (IH, s) , 7.06 (IH, t) , 7.29 (IH, d) , 7.52 (IH, t) , 8.31 (IH, d) , 9.95 (IH, s) , 12.18 (IH, br s) ; IR (solid) 2925,' 2852, 1622, 1590, 1581, 1558, 1494, 1481, 1453, 1435, 1394; MS 349.2 (M+H)+.
Example 340 [2- (l,4-Dioxa-8-aza-spiro [4,5] dec-8-yl) - quinazolin-4-yl] - (5-methyl-2ff-pyrazol-3-yl) -amine (III- 112): mp 191°C; XH NMR (DMSO) δ 1.65 (4H, s.) , 2.26 (3H, S) , 3.90 (4H, s) , 3.93 (4H, s) , 6.43 (IH, br s) , 7.09 (IH, t) , 7.32 (IH, d) , 7.54 (IH, t) , 8.35 (IH, d) , 9.99 (IH, br s) , 12.13 (IH, br s) ; IR (solid) 3069, 2964, 2927, 2868, 1618, 1581, 1568, 1540, 1495, 1481, 1435, 1390; MS 367.3 (M+H)+.
Example 341 [2- (4-Cyclopentylamino-piperidin-l-yl) - quinazolin-4-yl] - (5-methyl-2ff-pyrazol-3-yl) -amine (III- 113): mp 191°C; XH NMR (DMSO) δ 1.33 (2H, d) , 1.65 (4H, s) , 1.87 (2H, d) , 2.20 (IH, s) , 2.26 (3H, s) , 2.49 (2H, s) , 3.00 (2H, t) , 3.36 (2H, s) , 4.61 (2H, d) , 6.45 (IH, br s) , 7.07 (IH, s) , 7.31 (IH, d) , 7.52 (IH, s) , 8.33 (IH, d) , 9.94 (IH, br s) , 12.12 (IH, br s) ; IR (solid) 3371, 2943, 1622, 1600, 1581, 1545, 1509, 1463, 1440, 1390; MS 378.2 (M+H)+.
5 Example 342 [2- (4-Hydroxypiperidin-l-yl) -quinazolin-4- yl] - (5-methyl-2ff-pyrazol-3-yl) -amine (III-114) : mp 123°C; XH NMR (DMSO) δ 1.34 (2H, d) , 1.80 (2H, d) , 2.26 (3H, s) , 3.24 (2H, t) , 3.72 (IH, br s) , 4.39 (2H, d) , 4.70 (IH, d) , 6.44 (IH, br s) , 7.07 (IH, t) , 7.30 (IH, d), 7.53 10 (IH, t) , 8.33 (IH, d) , 9.94 (IH, br s) , 12.11 (IH, br s) ; IR (solid) 3265, 3151, 2927, 2863, 1622, 1600, 1572, 1540, 1504, 1476, 1440, 1390, 1349, 1066, 1098; MS 325.3 (M+H)+.
15 Example 343 (5-Cyclopropyl-2ff-pyrazol-3-yl) - [2- (4- hydroxy-4-phenylpiperidin-l-yl) -quinazolin-4-yl] -amine (III-115) : mp 131°C; XH NMR (DMSO) δ 0.64 (2H, q) , 0.93 (2H, q) , 1.68 (2H, d) , 1.83-1.97 (3H, m) , 3.20-3.45 (2H, m) , 4.69 (2H, d) , 5.11 (IH, s) , 6.37 (IH, br s) , 7.08 ,20 (IH, t)', 7.20 (IH, t) , 7.31 (3H, t) , 7.49 (2H, d) , 7.53
(IH, t) , 8.33 (IH, d) , 9.98 (IH, br s) , 12.18 (IH, br s) ; IR (solid) 3362, 2952, 2934, 2911, 2870, 2825, 1618, ■ 1584, 1570, 1559, 1536, 1481, 1459, 1431, 1372, 1336, 1213, 994; MS 427.6. (M+H) + .
25
Example 344 (5-Cyclopropyl-2ff-pyrazol-3-yl) - [2- (1,3- dihydro-isoindol-2-yl) -quinazolin-4-yl] -amine (III-116) : Prepared according to Method E-I to afford an off-white solid, mp 237°C; XH NMR (DMSO-d6) δ 0.79 (2H, s) , 1.00
30 (2H, d) , 1.99 (IH, m) , 4.92 (4H, d) , 6.72 (IH, br s) ,
7.13 (IH, t) , 7.33 (2H, s) , 7,30-7.48 (3H, m) , 7.58 (IH, t) , 8.40 (IH, d) , 10.12 (IH, s) , 12.17 (IH, s) ; IR (solid) 3449, 3318, 2850, 1623, 1595, 1577, 1541, 1509, 1482, 1432, 1391, 1359, 1141, 1027, 877, 814; MS 369.4 (M+H) + .
Example 345 (2-Azepan-l-yl) -quinazolin-4-yl] - (5- cyclopropyl-2ff-pyrazol-3-yl) -amine (III-117) : mp 199-
200°C; XH NMR (DMSO-d6) δ 0.60-0.70 (2H, m) , 0.90-1.00 (2H, m) , 1.45-1.57 (4H, m) , 1.70-1.85 (4H, m) , 1.88-1.97 (IH, m) , 3.75-3.87 (4H, m) , 6.42 (IH, s) , 7.02 (IH, t) , 7.27 (IH, d) , 7.49 (IH, t) , 8.29 (IH, d) , 9.91 (IH, s) , 12.19 (IH, br s) ; IR (solid) 2929, 1624, 1595, 1581, 1563, 1542, 1498, 1482, 1440, 1426, 1397, 1356, 1305, 1000, 825, 754; MS 349.2 (M+H)+.
Example 346 (5-Cyclopropyl-2ff-pyrazol-3-yl) - [2- (3,4- dihydro-lff-isoquinolin-2-yl) -quinazolin-4-yl] -amine (III- 118): mp 182-184°C; XH NMR (DMSO) δ 0.75 (2H, d) , 1.02 (2H, d) , 1.96 (IH, m) , 2.89 (2H, m) , 4.05 (2H, m) , 4.94 (2H, s) , 6.46 (IH, s) , 7.10 (IH, t) , 7.21 (4H, d) , 7.37 (IH, d) , 7.55 (IH, d) , 8.36 (IH, d) , 10.05 (IH, s) , 12.23 (IH, br s) ; IR (solid) 1621, 1581, 1560, 1537, 1479, 1456, 1426, 1396, 1374, 1341, 1222; MS 383.3 (M+H)+.
Example 347 (5-Cyclopropyl-2ff-pyrazol-3 -yl) - [2- (2,3- dihydro-indol-1-yl) -quinazolin-4-yl] -amine (III-119) : mp 150-153°C; XH NMR (DMSO) δ 0.74 (2H, d) , 0.98 (2H, d) , 1.96 (IH, m) , 3.15 (2H, t) , 4.25 (2H, t) , 6.45 (IH, br s) , 6.88 (IH, t) , 7.09 (IH, t) , 7.20 (2H, m) , 7.53 (IH, d) , 7.65 (IH, t) , 8.43 (2H, br s) , 10.09 (IH, s) , 12.28 (IH, br s) ; IR (solid) 1621, 1588, 1577, 1564, 1537, 1487, 1455, 1425, 1386, 1259; MS 369.3 (M+H)+.
Example 348 (5-Cyclopropyl-2ff-pyrazol-3-yl) - [2- (4- hydroxymethylpiperidin-1-yl) -quinazolin-4-yl] -amine (III- 120): mp 142°C; XH NMR (DMSO) δ 0.67 (2H, d) , 0.96 (2H, d) , 1.10 (2H, q) , 1.55-1.70 (3H, m) , 1.91 (IH, m) , 2.85 (2H, t) , 3.28 (2H, s) , 4.48 (IH, s) , 4.76 (2H, d) , 6.34 (IH, s) , 7.06 (IH, t) , 7.30 (IH, d) , 7.52 (IH, t) , 8.31 (IH, d) , 9.96 (IH, s) , 12.19 (IH, s) ; IR (solid) 3363, 3000, 2927, 2854, 1618, 1604, 1573, 1536, 1509, 1477, 1436, 1395, 1354, 1314, 1241, 1186, 1091, 995, 941, 823; MS 365.8 (M+H)+.
Example 349 (5-Cyclopropyl-2ff-pyrazol-3 -yl) - [2- (3,4- dihydro-2ff-quinolin-l-yl) -quinazolin-4-yl] -amine (III- 121): mp 137-145°C; XH NMR (DMSO-d6) δ 0.55 (2H, d) , 0.88 (2H, d) , 1.78 (IH, m) , 1.92 (2H, t) , 2.75 (2H, t) , 4.04 (2H, t) , 6.20 (IH, br s) , 6.97 (IH, t) , 7.14 (IH, m) , 7.19 (IH, t) , 7.42 (IH, d) , 7.61 (IH, t) , 7.67 (IH, d) ,
8.43 (IH, d) , 10.04 (IH, s) , 12.21 (IH, br s) ; IR (solid) 1622, 1572, 1539, 1493, 1454, 1420, 1373, 1249; MS 383.3 (M+H)+.
Example 350 (5-Methoxycarbonyl-2ff-pyrazol-3-yl) - [2-
(piperidine-1-yl) -quinazolin-4-yl] -amine (III-122) : XH NMR
(500MHz, CDC13) δ 1.7-1.8 (6H, m) , δ 3.8 (4H, m) , δ 3.9 (3H, s) , δ 5.5 (IH, s) , δ 7.15 (IH, t) , δ 7.4 (IH, d) , δ 7.6 (IH, t) , δ 8.0 (IH, d) . HPLC-Method B, (starting with 95% H20) Rt 7.4 min; MS (ES+) 353.24 (M+H).
Example 351 [5- (Piperidine-1-carbonyl) -2ff-pyrazol-3-yl] - [2- (piperidine-1-yl) -quinazolin-4-yl] -amine (III-123) :
HPLC-Method B, (starting with 95% H20:0.1% TFA) Rt 8.0 min; MS (ES+) 406.30, (ES-) 404.30.
Example 352 (5-Hydroxymethyl-2ff-pyrazol-3-yl) - [2- (piperidin-1-yl) -quinazolin-4-yl] -amine (III-124) : To a solution of III-122 (10.0 mg, 0.028 mmol) in THF (6 mL) at ambient temperature was slowly added a IM solution of LiAlH4 in THF (0.05 mL, 0.05 mmol). After 15 minutes the solution was quenched with water and IN HCl. The product was extracted from the aqueous layer with EtOAc . The organic layer was dried over MgS04, filtered, and concentrated in vacuo. The residue was purified by preparatory HPLC to afford III-124 (4.0 mg, 44%). HPLC- Method B, (starting with 95% H2O:0.1% TFA) Rt 6.1 min; MS (ES+) 325.13 (M+H), (ES-) 323.13 (M-H).
Example 353 (5-Carbamoyl-2ff-pyrazol-3-yl) - [2- (piperidin- 1-yl) -quinazolin-4-yl] -amine (III-125) : A solution of III-122 (1.5 g, 4.3 mmol) in 2.0 M NH3/MeOH (100 mL) was heated at 110°C for 2 days. The dark brown reaction mixture was concentrated in vacuo to afford a viscous oil which was purified by column chromatography to yield 0.7 g (50%) of III-125. XH NMR (500MHz, CD30D-d3) δl.6 (4H, m) , δl.7 (2H, m) , δ 3.3 (IH, s) , δ 3.8 (4H, m) , δ 5.5 (IH, s) , δ 7.15 (IH, t) , δ 7.45 (IH, d) , δ 7.55 (IH, t) , δ 8.0 (IH, d) ; HPLC-Method B, (starting with 95% H2O:0.1% TFA) Rt 5.9 min; MS (ES+) 338.13, (ES-) 336.15.
Example 354 (5-Carbamoyl-2ff-pyrazol-3-yl) - [2- (4- methylpiperidin-1-yl) -quinazolin-4-yl] -amine (III-126) :
HPLC-Method B, (starting with 95% H2O:0.1% TFA) Rt 6.4 min; MS (ES+) 352.19, (ES-) 350.20.
Example 355 (5, 7-Difluoro-lff-indazol-3-yl) - (2-phenyl- 5,6,7,8-tetrahydroquinazolin-4-yl) -amine (III-127) : XH NMR (500 MHz, DMSO-d6) δ 13.7 (s, IH) , 10.3 (s, br, IH) , 7.90 (d, 2H) , 7.52 (t, IH) , 7.45 (m, 3H),.7.26 (d, IH) , 2.99 (m, 2H) , 2.75 (m, 2H) , 1.95 (br, 4H) ppm; MS (ES+) 378.24 (M+H); (ES-) 376.23 (M-H); HPLC-Method A, Rt 3.04 min.
Example 356 (2-Phenyl-5, 6, 7, 8-tetrahydroquinazolin-4-yl) - (5-trifluoromethyl-Iff-indazol-3-yl) -amine (III-128) : XH
NMR (500 MHz, DMSO-d6) δl3.4 (s, IH) , 10.2 (s, br, IH) , 8.13 (s, IH) , 7.86 (d, 2H) , 7.78 (d, IH) , 7.69 (d, IH) , 7.50 (t, IH) , 7.35 (dd, 2H) ", 2.89 (m, 2H) , 2.72 (m, 2H) , 1.90 (s, br, 4H) ppm; MS (ES+) 410.24 (M+H); (ES-) 408.23 (M-H); HPLC-Method A, Rt 3.19 min.
Example 357 (7-Fluoro-Iff-indazol-3-yl) - (2-phenyl- quinazolin-4-yl) -amine (III-129) : XH NMR (500 MHz, DMSO- d6) δl3.6 (s, IH) , 11.1 (s, br, IH) , 8.65 (d, IH) , 8.03 (d, 2H) , 7.95 (s, 2H) , 7.67 (m, IH) , 7.45 (m, 2H) , 7.33
(t, 2H) , 7.22 (dd, IH) , 6.99 (td, IH) ppm. MS (ES+) : m/e= 356.20 (M+H); HPLC-Method A Rt 3.00 min.
Example 358 (5-Fluoro-Iff-indazol-3-yl) - (2-phenyl- quinazolin-4-yl) -amine (III-130) : XH NMR (500 MHz, DMSO- d6) δl3.2 (s, IH) , 11.3 (s, br, IH) , 8.67 (d, IH) , 8.04 (d, 2H) , 7.96 (s, 2H) , 7.70 (m, IH) , 7.58 (dd, IH) , 7.43 (m, 4H) , 7.28 (td, IH) ppm. MS (ES+) 356.20 (M+H); HPLC- Method A, Rt 3.00 min.
Example 359 (5, 7-Difluoro-Iff-indazol-3 -yl) - (2 -phenyl- quinazolin-4-yl) -amine (III-131) : XH NMR (500 MHz, DMSO- d6) δl3.7 (S, IH) , 8.65 (d, IH) , 8.04 (d, 2H) , 7.95 (s, 2H) , 7.68 (m, IH) , 7.45 (m, IH) , 7.35 (m, 4H) ppm. MS (ES+) : m/e= 374.17 (M+H); HPLC-Method A, Rt 3.07 min.
Example 360 (Iff-Indazol-3 -yl) - [2- (3-trifluoromethylphenyl) -quinazolin-4-yl] -amine (III-132) : XH NMR (500MHz, DMSO-d6) δ 7.06 (t, IH) , 7.42 (t, IH) , 7.59 (d, IH) , 7.63 (t, IH) , 7.66 (d, IH) , 7.71 (m, IH) , 7.80 (d, IH) , 7.98 (m, 2H) , 8.33 (s, IH) , 8.46 (d, IH) , 8.71 (d, IH) , 11.04 (br. S, IH) , 12.97 (s, IH) ; EI-MS 406.1 (M+l); HPLC- Method A, Rt 3.15 min.
Example 361 (2-Phenyl-quinazolin-4-yl) - (lff-pyrazolo [4, 3- b]pyridin-3-yl) -amine (III-133) : XH NMR (500 MHz, DMSO-d6) δl3.3 (s, br, IH) , 11.4 (s, br, IH) , 8.78 (d, IH) , 8.58 (dd, IH) , 8.24 (d, IH) , 8.10 (m, 2H) , 7.95 (d, 2H) , 7.86
(t, IH) , 7.56 (m, 2H) , 7.44 (t, 2H) ppm. MS (ES+) 339.11
(M+H); HPLC-Method A, Rt 2.63 min.
Example 362 [5- (3-Methoxy-phenyl) -6-oxo-5, 6-dihydro-lH- pyrazolo [4, 3-c] yridazin-3-yl] - (2-phenyl-quinazolin-4- yl)-amine (III-134) : XH NMR (500 MHz, MeOH-d4) δ8.65 (d, IH) , 8.17 (m, 3H) , 8.10 (d, IH) , 7.90 (t, IH) , 7.75 (t, IH) , 7.58 (m, 2H) , 7.25 (t, IH) , 6.95 (m, 2H) , 6.85 (d, IH) , 6.80 (s, IH) , 3.64 (s, 3H) ppm. MS (ES+) : m/e= 462.2 (M+H) .
Example 363 (6-Oxo-5-phenyl-5, 6-dihydro-IH- yrazolo [4,3- c]pyridazin-3-yl) - (2-phenyl-quinazolin-4-yl) -amine (III- 135): H NMR (500 MHz, MeOH-d4) δ8.61 (d, IH) , 8.13 (m, 3H) , 8.05 (d, IH) , 7.85 (t, IH) , 7.70 (t, IH) , 7.58 (m, 2H) , 7.32 (m, 5H) , 6.79 (s, IH) ppm. MS (ES+) : m/e= 432.2 (M+H) .
Example 364 [5- (4-Methoxy-phenyl) -6-oxo-5, 6-dihydro-lH- pyrazolo [4, 3-c] yridazin-3 -yl] - (2-phenyl-quinazolin-4- yl) -amine (III-136) : MS (ES+) 462.2 (M+H). Example 365 [5- (2,4-Dichloro-phenyl) -6-oxσ-5, 6-dihydro- lH-pyrazolo[4,3-c]pyridazin-3-yl] - (2-phenyl-quinazolin-4- yl)-amine (III-137) : XH NMR (500 MHz, MeOH-d4) δ8.63 (d, IH) , 8.17 (m, 4H) , 7.89 (t, IH) , 7.73 (t, IH) , 7.61 (t, 2H) , 7.57 (d, IH) , 7.32 (m, IH) , 7.21 (d, IH) , 6.84 (s, IH) ppm. MS (ES+) : m/e= 500.1 (M+H).
Example 366 [6-Oxo-5- (3-trifluoromethyl-phenyl) -5,6- dihydro-lH-pyrazolo [4, 3-c]pyridazin-3-yl] - (2-phenyl- quinazolin-4-yl) -amine (III-138) : XH NMR (500 MHz, MeOH- d4) δ8.55 (d, IH) , 8.19 (d, 2H) , 7.92 (m, 2H) , 7.65 (m, 3H) , 7.45 (t, 2H) , 7.25 (t, IH) , 7.13 (t, IH) , 7.05 (t, IH) , 6.75 (s, IH) ppm. MS (ES+) : m/e= 500.2 (M+H).
Example 367 [6-Oxo-5- (4-Phenoxy-phenyl) -5, 6-dihydro-lH- pyrazolo [4, 3-c]pyridazin-3-yl] - (2-phenyl-quinazolin-4- yl) -amine (III-139) : MS (ES+) 524.3 (M+H).
Example 368 [5- (4-Chloro-phenyl) -6-oxo-5, 6-dihydro-lH- pyrazolo [4, 3-c] yridazin-3-yl] - (2-phenyl-quinazolin-4- yl) -amine (III-140) : MS (ES+) 466.2 (M+H).
Example 369 (2-imidazol-l-yl-quinazolin-4-yl) - (lff- indazol-3-yl) -amine (III-141) : XH NMR (500MHz, DMSO-d6) δ 7.10 (t, IH) , 7.44 (t, IH) , 7.50 (br. s, IH) , 7.60 (d, IH) , 7.72 (m, 2H) , 7.77 (m, IH) , 7.88 (d, IH) , 7.98 (t, IH) , 8.73 (d, IH) , 8.96 (s, IH) , 11.23 (s, IH) , 13.06 (s, IH) ; EI-MS 328.1 (M+l); HPLC-Method A, Rt 2.93 min.
Example 370 (lff-Indazol-3-yl) - [2- (2-methyl-imidazol-l-yl- guinazolin-4-yl] -amine (III-142) : XH NMR (500MHz, DMSO-d6) δ 2.48 (s, 3H) , 7.10 (t, IH) , 7.43 (t, IH) , 7.57 (d, IH) , 7.60 (d, IH) , 7.67 (d, IH) , 7.76 (td, IH) , 7.86 (d, IH) , 7.91 (d, IH) , 8.01 (td, IH) , 8.72 (d, IH) , 11.15 (s, IH) , 13.10 (s, IH) ; EI-MS 342.1 (M+l); HPLC-Method A, Rt 3.06 min.
Example 371 (Iff-Indazol-3 -yl) - (2-piperidin-l-yl- quinazolin-4-yl) -amine (III-143) : XH NMR (500MHz, DMSO-d6) δ 1.48 (m, 6H) , 3.60 (m, 4H) , 7.11 (t, IH) , 7.52 (t, IH) , 7.55 (d, IH) , 7.64 (d, IH) , 7.69 (d, IH) , 7.75 (d, IH) , 7.90 (t, IH) , 8.58 (d, IH) , 11.82 (br. s, IH) , 13.25 (s, IH) ; EI-MS 345.1 (M+l); HPLC-Method A, Rt 3.03 min.
Example 372 (Iff-Indazol-3-yl) - [2- (octahydro-quinolin-1- yl) -quinazolin-4-yl] -amine (III-144) : XH NMR (500MHz, DMSO-d6) δ 0.6-1.9 (m, 13 H) , 3.15 (m, IH) , 3.25 (m, IH) , 4.0 (m, IH) , 7.10 (t, 0.5H), 7.12 (t, 0.5H), 7.55 (m,
2H) , 7.66 (d, 0.5 H) , 7.69 (d, 0.5 H) , 7.77 (d, IH) , 7.91 (t, IH) , 8.55 (d, 0.5 H) , 8.59 (d, 0.5 H) , 11.46 (s, 0.5 H) , 11.54 (s, 0.5 H) , 11.78 (s, 0.5 H) , 11.84 (s, 0.5 H) , 13.10 (s, 0.5 H) , 13.12 (s, 0.5 H) ; EI-MS 399.3 (M+l) ; HPLC-Method A, Rt 3.37 min.
Example 373 (Iff- Indazol- 3 -yl) - [2- (2, 6 -dimethyl -morpholin- 4-yl) -quinazolin-4-yl] -amine (III-145) : XH NMR (500MHz, DMSO-d6) δ 1.0 (m, 6H) , 4.0 (m, 6H) , 7.12 (t, IH), 7.41 (td, IH) , 7.56 (t, IH) , 7.58 (d, IH) , 7.68 (dd, IH) , 7.77 (t, IH) , 7.93 (t, IH) , 8.60 (d, IH) , 11.69 (s, IH) , 13.16 (s, IH) ; EI-MS 375.3 (M+l); HPLC-Method A, Rt 2.93 min.
Example 374 (5-Methyl-2ff-pyrazol-3-yl) - (2 -phenyl - pyrimidin- 4-yl) -amine (IV-1) : mp 245-246°C; XH NMR (DMSO) δ 2.26 (3H, s) , 6.32 (IH, br s) , 7.07 (IH, br s) , 7.48- 7.54 (3H, m) , 8.33-8.39 (3H, m) , 9.87 (IH, s) , 12.03 (IH, s) ; IR (solid) 1628, 1589, 1579, 1522, 1479, 1441, 1393, 1336; MS 252.2 (M+H)+.
Example 375 [6- (4-Acetamidophenylsulfanyl) -2-phenyl- pyrimidin-4-yl] - (5-methyl-2ff-pyrazol—3-yl) -amine (IV-3) :
A suspension of Fenclorim (4 , 6-dichloro-2- phenylpyrimidine) (0.lg, 0.44 mmol), 3-amino-5- methylpyrazole (0.045 g, 0.47 mmol), N, N- diisopropylethyla ine (0.08 ml, 0.47 mmol) and sodium iodide (0.067 g, 0.44 mmol) in n-butanol (5 ml) were heated at 117 °C for 18 hours. The solvent was removed in vacuo and the crude product purified by flash chromatography (silica gel, 3:2 Petrol:EtOAc) to afford 0.037 g (29 % yield) of (6-Chloro-2-phenyl-pyrimidin-4- yl) - (5-methyl-2ff-pyrazol—3-yl) -amine as a off-white solid. A suspension of the above pyrimidine (0.037 g, 0.13 mmol) and thioacetamidothiophenol (0.108 g, 0.64 mmol) in tert-butanol was heated at 85 °C under nitrogen for 2 days . The reaction mixture was cooled to room temperature and the solvent removed in vacuo. The concentrate was dissolved in EtOAc, and washed with NaHC03 (sat, aq. ) . The organic layer is concentrated in vacuo, and the crude product by preperative HPLC. The residual disulfide that still remained in the mixture after HPLC may be removed by precipitation from EtOAc and filtration. The mother liquor was concentrated to afford IV-3 (7mg, 13 % yield) as an off-white solid: mp 235- 236°C; XH NMR (DMSO) δ 2.10 (3H, s) , 2.21 (3H, s) , 6.33 (IH, br s) , 7.50 (3H, m) , 7.7-7.59 (2H, m) , 7.76-7.78 (2H, m) , 8.25 (2H, m) , 9.72, 10.26 and 11.93 (3 H, 3 x br s) ; IR (solid) 1669, 1585, 1551, 1492, 1392, 1372, 1312, 1289, 1259, 1174, 1102, 1089, 1027, 1015, 984; MS 417.3 (M+H) + . Example 376 [2- (4-Methylpiperidin-l-yl) -pyrimidin-4-yl] - (5-methyl-2ff-pyrazol-3-yl) -amine (IV-4) : mp 215-216°C; XH NMR (CD3OD) δ 0.96 (3H, d) , 1.16 (2H, m) , 1.66 (3H,- m) , 2.27 (3H, S) , 2.86 (2H, t) , 4.58 (2H, m) , 4.78 (2H, exch. rotons) , 6.13 (2H, m) , 7.83 (IH, d) ; IR (solid) 1593, 1550, 1489, 1436, 1331, 1246, 1231; MS 273.1 (M+H)+.
Example 377 [2- (4-Methylpiperidin-l-yl) -5-nitropyrimidin- 4-yl] - (5-methyl-2ff-pyrazol-3-yl) -amine (IV-5): mp 185- 187°C; XH NMR (DMSO) δ 0.93 (3H, d) , 1.06-1.18 (2H, m) , 1.68-1.80 (3H, m) , 2.26 (3H, s) , 3.01-3.12 (2H, m) , 4.63 (IH, d) , 4.80 (IH, d) , 6.39 (IH, s) , 9.00 (IH, s) , 10.41 (IH, s) , 12.36 (IH, s) ; IR (solid) 1589, 1517, 1479, 1446, 1346, 1317, 1246, 1222, 1055; MS 318.2 (M+H)+.
Example 378 [5-Amino-2- (4-Methylpiperidin-l-yl) - pyrimidin-4-yl] - (5-methyl-2ff-pyrazol-3-yl) -amine (IV-6) :
To a solution of IV-5 (48 mg, 0.151 mmol) in ethanol (2.0 mL) was added tin dichloride dihydrate (171 mg, 0.756 mmol) and the resulting mixture heated at reflux for 3 hours . The reaction was cooled to room temperature and poured onto a mixture of IM NaOH-.dichloromethane -.propanoi (18:8:4mL). and stirred for 15 minutes. The layers were separated and the aqueous layer extracted twice with dichloromethane. The combined organic layers were concentrated in vacuo and the residue purified by flash chromatography (silica gel, gradient dichloromethane:MeOH) to afford IV-6 as a grey solid (27mg, 63%): XH NMR (DMSO) δ 0.88-1.04 (5H, m) , 1.55-1.62 (3H, m) , 2.21 (3H, s) , 2.70 (2H, m) , 3.36 (2H, m) , 4.40 (2H, m) , 6.37 (IH, s) , 7.49 (IH, s) , 8.40 (IH, s) , 11.92 (IH, br s) ; MS 288.2 (M+H)+. Example 379 [5-Amino-6-methyl-2- (4-methylpiperidin-l-yl) - pyrimidin-4-yl] - (5-methyl-2ff-pyrazol-3-yl) -amine (IV-7) : mp 172-175°C; XH NMR (DMSO) δ 0.90 (3H, d) , 1.03 (2H, m) , 1.52-1.62 (3H, m) . 2.13 (3H, s) , 2.20 (3H, s) , 2.69 (2H, m) , 3.92 (2H, br s) , 4.44 (2H, d) , 6.35 (IH, s) , 8.41 (IH, s) , 11.85 (IH, br s) ; IR (solid) 1612, 1589, 1489, 1446, 1317; MS 302.5 (M+H)+.
Example 380 [6-Methyl-2- (4-methyl-phenyl) -pyrimidin-4- yl] -(5-phenyl-2ff-pyrazol-3-yl) -amine (IV-10) : MS 342.34 (M+H); HPLC-Method E, Rt 1.334 min.
Example 381 [2- (4-Chloro-phenyl) -6-methyl-pyrimidin-4- yl] - (5-furan-2-yl-2ff-pyrazol-3-yl) -amine (IV-11): MS
352.11 (M+H); HPLC Method E, Rt 1-194 min.
Example 382 5-Furan-2-yl-2ff-pyrazol-3-yl) - (6-methyl-2- phenyl-pyrimidin-4-yl) -amine (IV-12) : MS 318.21 (M+H); HPLC-Method E, 1.192 min.
Example 383 [6-Methyl-2- (4 -trifluoromethyl-phenyl) - pyrimidin- -yl] - (5-phenγl-2-yl-2ff-pyrazol-3-yl) -amine
(IV-13) : MS .396.24 (M+H); HPLC-Method E, Rt 1.419 min.
Example 384 (5-Furan-2-yl-2ff-pyrazol-3-yl) - [6-methyl-2-
(4-trifluoromethyl-phenyl) -pyrimidin-4-yl] -amine (IV-14) : MS 386.08 (M+H); HPLC-Method E 1.347 min.
Example 385 [2- (2, 3 -Dihydro-benzo [1,4] dioxin-2-yl) -6- methyl-pyrimidin-4-yl] - (5-furan-2-yl-2ff-pyrazol—3-yl) - amine (IV-15) : MS 376.18 (M+H); HPLC-Method E, Rt 1.181 min. Example 386 [2- (2, 3-Dihydro-bezo [1,4] dioxin-2-yl) -6- ethyl-pyrimidin-4-yl] - (5-methyl-2ff-pyrazol—3-yl) -amine (IV-16) : MS 338.17 (M+H); HPLC-Method E, Rt 1.082 min.
Example 387 (6-Ethyl-2-phenyl-pyrimidin-4-yl) - (5-methyl- 2ff-pyrazol-3-yl) -amine (IV-17) : MS 280.18 (M+H); HPLC- Method E, Rt 1.024 min.
Example 388 (6-Methyl-2-phenyl-pyrimidin-4-yl) - (5-phenyl- 2ff-pyrazol-3-yl) -amine (IV-19) : MS 328.51 (M+H); HPLC- Method E, Rt 1.192 min.
Example 389 [6-Ethyl-2- (4 -trifluoromethyl-phenyl) - pyrimidin-4-yl] - (5-methyl-2ff-pyrazol-3-yl) -amine (IV-20):
MS 348.5 (M+H); HPLC-Method E, Rt 1.224 min.
Example 390 (5-Furan-2-yl-2H-pyrazol-3-yl) - [6-methyl-2- (4-methyl-phenyl) -pyrimidin-4-yl] -amine (IV-21) : MS 332.23 (M+H); HPLC-Method E, Rt 1.139 min.
Example 391 (6-Methoxymethyl-2-phenyl-pyrimidin-4-yl) - (5- methyl-2ff-pyrazol-3-yl) -amine (IV-22) : MS 296.31 (M+H); HPLC-Method E, Rt 0.971 min.
Example 392 (5, 6-Dimethyl-2-phenyl-pyrimidin-4-yl) - (5- methyl-2ff-pyrazol-3-yl) -amine (IV-23) : MS 280.2 (M+H); HPLC-Method E, Rt 0.927 min.
Example 393 (6-Methyl-2 -phenyl-pyrimidin-4-yl) - (5-methyl■ 2ff-pyrazol-3-yl) -amine (IV-24) : MS 266.18 (M+H); HPLC- Method E, Rt 0.925 min. Example 394 [6-Ethyl-2- (4-methyl-phenyl) -pyrimidin-4-yl] - (5-methyl-2ff-pyrazol-3-yl) -amine (IV-25) : MS 294.46 (M+H); HPLC-Method E, Rt 1.174 min.
Example 395 [2- (4-Chloro-phenyl) -6-ethyl-pyrimidin-4-yl] - (5-methyl-2ff-pyrazol-3-yl) -amine (IV-26) : MS 314.42 (M+H); HPLC-Method E Rt 1.213 min.
Example 396 (5-Methyl-lH-pyrazol-3-yl) - (6-methyl-2-p- tolyl-pyrimidin-4-yl) -amine (IV-27) : MS 280.45 (M+H); HPLC-Method E, Rt 1.135 min.
Example 397 (Iff-Indazol-3-yl) - (6-methoxymethyl-2-phenyl- pyrimidin-4-yl) -amine (IV-28) : XH NMR (500 MHz, DMSO) δ 3.57 (3H, s) , 4.65 (2H, s) , 7.23 (IH, J=7.5 Hz, t) , 7.52
(IH, J=7.6 Hz, t) , 7.63 (4H, m) , 7.75 (IH, br) , 8.13 (IH, J=5.5 Hz, br d) , 8.44 (IH, J=5.7 Hz, br d) , 10.6 (IH, br) , 12.8 (IH, br s) ppm; HPLC-Method A, Rt 2.944 min; MS
(FIA) 332.1 (M+H)+.
Example 398 (5-Methyl-2ff-pyrazol-3-yl) - (2-pyridin-4-yl- thieno[3,2-d]pyrimidin-4-yl) -amine (IV-29) : XH NMR (DMSO) δ 2.34 (3H, s) , 6.66 (IH, s) , 7.53 (IH, d) , 7.84,(1H, d) , 8.32 (2H, d) , 8.70 (2H, d) ; MS 309.6 (M+H)+.
Example 399 (5-Methyl-2ff-pyrazol-3-yl) - (2-phenyl- pyrido [3, 4-d] pyrimidin -4-yl) -amine (IV-30): mp 225°C; XH NMR (DMSO) δ 2.35 (3H, s) , 6.81 (IH, s) , 7.50-7.63 (3H, m) , 8.45-8.52 (2H, m) , 8.54 (IH, d) , 8.62 (IH, d) , 9.20 (IH, s) , 10.79 (IH, s) , 12.38 (IH, br s) ; IR (solid)
2958, 2917, 2852, 1593, 1565, 1524, 1467, 1450; MS 303.2 (M+H)+. Example 400 (5-Methyl-2ff-pyrazol-3-yl) - (2-phenyl- pyrido [2, 3-d] pyrimidin-4-yl) -amine (IV-31) :
To a solution of 4-chloro-2-phenyl-pyrido [2, 3- d]pyrimidine (J. Pharm. Belg., 29, 1974, 145-148) (109mg, 0.45 mmol) in THF (15 mL) was added 3 -amino-5-methyl pyrazole (48 mg, 0.5 mmol) and the resulting mixture heated at 65 °C overnight. The mixture was cooled to room temperature and the resulting suspension was filtered and washed with Et20. The solid was dissolved in a mixture EtOH: water and the pH adjusted to pH 7. The aqueous was extracted twice with ethyl acetate and the combined organic layers were dried (MgS04) , filtered, and concentrated in vacuo. The residue was purified by flash chromatography (Si02, DCM-MeOH gradient) to afford IV-31 as an .off-white solid (69 mg, 50%) : mp 234°C; XH NMR
(DMSO) δ 2.14 (3H, s) , 5.99 (IH, s) , 7.20-7.40 (3H, m) , 7.40-7.50 (3H, m) , 8.60 (IH, d) , 8.79 (IH, d) , 12.82 (IH, br s) ; IR (solid) 2957, 2921, 2857, 1644, 1560, 1459, 1427; MS 303.2 (M+H)+.
Example 401 (5-Cyclopropyl-2ff-pyrazol-3-yl) - (2-phenyl- pyrido [3, 4-d] pyrimidin-4-yl) -amine (IV-32) : off-white solid, mp 232-233°C; XH NMR (DMSO) δ 0.70-0.85 (2H, m) , 0.90-1.05 (2H, m) , 1.05-2.07 (IH, m) , 6.75 (IH, s) , 7.50- 7.75 (3H, m) , 8.40-8.70 (4H, m) , 9.20 (IH, s) , 10.80 (IH, s) , 12.41 (IH) ; IR (solid) 3178, 1601, 1573, 1532, 1484, 1452, 1409, 1367, 1328, 802, 781, 667; MS 329.2 (M+H)+.
Example 402 [2- (4-Methylpiperidin-l-yl) -purin-4-yl] - (5- methyl-2ff-pyrazol-3-yl) -amine (IV-33): To a suspension of 2,4-dichloro-purine (2.0 g, 10.6 mmol) in anhydrous ethanol (10 mL) was added 5-methyl-lff-pyrazol-3-yl amine (2.05 g, 21.2 mmol). The resulting mixture was stirred at room temperature- for 48 h. The resulting precipitate was collected by filtration, washed with ethanol, and dried under vacuum to afford 1.524 g (58% yield) of (2- chloro-purin-4-yl) - (5-methyl-lff-pyrazol-3-yl) -amine which was used in the next step without further purification. To a solution of (2-chloro-purin-4-yl) - (5-methyl-lff- pyrazol-3-yl) -amine (200 mg, 0.80 mmol) was added 4- methylpiperidine (4 mL, 8.01 mmol) and the reaction mixture heated at reflux overnight. The solvent was evaporated and the residue dissolved in a mixture
EtOH:water (1:3, 4 mL) . Potassium carbonate (57mg, 0.41 mmol) was added and the mixture was stirred at room temperature for 2 hours. The resulting suspension was filtered, washed with water (x2) and rinsed with Et20 (x2) to afford IV-33 as a white solid (225mg, 90%) : mp >300°C; XH NMR (DMSO) δ 0.91 (3H, d) , 1.10 (2H, m) , 1.65 (3H, m) , 2.24. (3H, s) , 2.84 (2H, m) , 4.60 (2H, m) , 6.40 (IH, s) , 7.87 (IH, m) , 9.37-9.59 (IH, m) , 12.03-12.39 (2H, m) ; IR (solid) 1651, 1612, 1574, 1484, 1446, 1327, 1317, 1255, 1203; MS 313.3 (M+H)+.
Example 403 (5 -Cyclopropyl -2ff-pyrazol -3-yl) - [2- (4- methylpiperidin-1-yl) -pyrrolo [3, 2-d]pyrimidin-4-yl] -amine
(IV-34) : white solid; XH NMR (DMSO) δ-0.65 (2H, m) , 0.91- 0.96 (5H, m) , 1.08 (2H, m) , 1.58-1.64 (3H, m) , 1.89 (IH, m) , 2.77 (2H, t) , 4.57 (2H, d) , 6.09 (IH, s) , 6.38 (IH, s) , 7.33 (IH, s) , 9.42 (IH, s) , 10.65 (IH, s) , 12.02 (IH, br s) ; MS 338.3 (M+H)+.
Example 404 [ 6 -Benzyl -2 -phenyl -5, 6, 7, 8 -tetrahydro - pyrido [4,3-d]pyrimidin-4-yl] - (5 -fluoro- Iff- indazol-3-yl) - amine (IV-35) : XH NMR (500 MHz, DMSO-d6) δ 13.0 (s, IH) , 10.4 (s, br, IH) , 9.73 (s, IH, TFA-OH) , 8.00 (d, 2H) , 7 . 64 (m, 2H) , 7 . 59 (dd, IH) , 7 . 52 (m, 3H) , 7 . 41 (t , IH) , 7 . 31 (m, 3H) , 7 . 14 (dd, IH) , 4 . 58 ( s , 2H) , 4 . 35 (br , 2H) , 3 . 74 (m, 2H) , 3 . 17 ( s , 2H) ppm . MS (ES+) : m/e= 451 . 30
(M+H); HPLC-Method A, Tret 2.96 min.
Example 405 (5-Fluoro-Iff-indazol-3-yl) - (2-phenyl-5, 6,7,8- tetrahydro-pyrido [4, 3-d] pyrimidin-4-yl) -amine (IV-36) : Prepared from IV-35 (0.13 mmol) by treatment with an equal weight of Pd/C (10%) in 4.4% HCOOH in MeOH at room temperature for 12 h. The mixture was filtered through celite, the filtrate was evaporated, and crude product was purified by HPLC to afford IV-36 as yellow solid in 35% yield. XH NMR (500 MHz, DMSO-d6) δ 12.9 (s, IH) , 9.06
(s, IH) , 7.99 (d, 2H) , 7.57 (dd, IH) , 7.34 (m, IH) , 7.28 (m, 3H) , 7.22 (d, IH) , 3.83 (s, 2H) , 3.05 (m, 2H) , 2.72
(m, 2H) ppm. MS (ES+) : m/e= 361.20 (M+H); HPLC-Method A, Tret 2.68 min.
Example 406 (5-Methyl-2ff-pyrazol—3-yl) - (3-phenyl- isoquinolin-1-yl) -amine (V-1) : To a solution of 1-chloro- 3-phenylisoquinoline (J. Het. Chem., 20, 1983, 121- 128) (0.33g, 1.37 mmol) in DMF (anhydrous, 5 L) was added 3-amino-5-methylpyrazole (0.27g, 2.74 mmol) and potassium carbonate (0.57g, 4.13 mmol) and the resulting mixture was heated at reflux for 6 hours. The reaction mixture was then cooled and solvent removed in vacuo. The residue was extracted twice with ethyl acetate and the combined organic layers washed with brine, dried (MgS0 ) , filtered and concentrated in vacuo. The crude product was purified by flash chromatography (Si02, gradient DCM-MeOH) to afford V-1 as a colourless oil; XH NMR (MeOD) δ 2.23 (3H, s) , 5.61 (IH, s) , 7.41 (IH, m) , 7.52(2H, m) , 7 . 62 ( 1H , m) , 7 . 81 ( 1H, m) , 8 . 07 ( 1H, d) , 8 . 19 ( 2H, m) , 8 . 29 ( 1H , s) , 8 . 54' ( IH , d) ; MS 301 . 2 (M+H) + .
Example 407 (Iff-Indazol-3-yl) - [3- (2-trifluoromethyl- phenyl) -isoquinoline-1-yl] -amine (V-2) : A solution of 1- chloro-3- (2-trifluoromethyl-phenyl) -isoquinoline (100 mg, 0.326 mmol) and Iff-indazol-3 -ylamine (86 mg, 0.651 mmol) in ethanol (3 mL) was heated at 160 C and the solvent evaporated with a stream of nitrogen. The remaining oil was then heated at 160 C for 18 hours under nitrogen. The resulting melt was dissolved in 5% methanol: dichloromethane (50 mL) , washed with saturated aqueous sodium bicarbonate (1 x 25 mL) then dried over magnesium sulfate. Purification by silica gel chromatography (25% to 50% hexane: ethyl acetate) afforded V-2 as a yellow solid (35 mg, 27%). XH NMR (500 MHz, d6- DMSO) δ 9.78 (br s, IH) , 8.62 (d, IH) , 7.9-7.85 (m, IH) , 7.78-7.72 (m, IH) , 7.70-7.68 (m, IH) , 7.65-7.62 (m, IH) , 7.60-7.55 (m, IH) , 7.52-7.45 (m, 3H) , 7.41-7.38 (m, IH) , 7.28-7.25 (m, IH) , 7.18 (s, IH) , 6.95-6.92 (m, IH) , 5.76 (s, IH) ; LC-MS (ES+) m/e= 405.18 (M+H); HPLC-Method D Rt 2.74 min.
Example 408 (5,7-Difluoro-Iff-indazol-3-yl) - [3- (2- trifluoromethyl-phenyl) -isoquinolin-1-yl] -amine (V-3) -.
Prepared from 5, 7-difluoro-Iff-indazol-3 -ylamineto afford compound V-3 as a yellow solid (90 mg, 63%) . XH NMR (500 MHz, de-DMSO) δ 13.25 (s, IH) , 9.92 (br s, IH) , 8.61 (d, IH) , 7.9 (d, IH) , 7.81-7.49 (m, 6H) , 7.26-7.2 (m, 2H) , 7.12-7.10 (m, IH) ; LC-MS (ES+) m/e= 441.16 (M+H); HPLC- Method D, Rt 3.58 min. Example 409 (5-Methyl-2ff-pyrazol-3-yl) - (2-phenyl- quinolin-4-yl) -amine (V-4): To a mixture of 4-chloro-2- phenylquinoline (J. Het. Chem., 20, 1983, 121-128) (0.53g, 2.21 mmol) in diphenylether (5 mL) was added 3-amino-5- methylpyrazole (0.43g, -4.42 mmol) and the resulting mixture heated at 200°C overnight with stirring. The reaction mixture was cooled to ambient temperature then petroleum ether (20 mL) was added and the resulting precipitate was isolated by filtration. The crude solid was purified by flash chromatography (Si02, gradient DCM- MeOH) to afford V-4 as a white solid: mp 242-244°C; XH NMR (DMSO) δ 2.27(3H, s) , 6.02(1H, s) , 7.47(2H, d) , 7.53- 7.40(2H br m) , 7.67 (IH, ) , 7.92 (IH, m) , 8.09(2H, d) , 8.48(2H, m) , 9.20(1H, s) , 12.17(1H, br s) ; IR (solid) ' 1584, 1559, 1554, 1483, 1447, 1430, 1389; MS 301.2 (M+H)+.
Example 410 (Iff-Indazol-3-yl) - (2-phenyl-quinolin-4-yl) - amine (V-5) : XH NMR (500 MHz, d6-DMSO) δ 12.78 (s, IH) , 9.50 (s, IH) , 8.65 (d, IH) , 8.15 (s, IH) , 8.04-7.98 ( , 3H) , 7.94 (s, IH) , 7.78-7.75 (m, IH) , 7.60-7.40 (m, 6H) , 7.15-7.10 (m, IH) . LC-MS (ES+) m/e= 337.11 (M+H); HPLC- Method D, Rt 2.10 min.
Example 411 (2-Phenyl-quinolin-4-yl) - (lff-pyrazolo [4,3- b]pyridin-3-yl) -amine (V-6) : XH NMR (500 MHz, DMSO-d6) δl3.6 (s, IH) , 11.4 (s, IH) , 8.94 (d, IH) , 8.61 (dd, IH) , 8.23 (d, IH) , 8.16 (dd, IH) , 8.12 (t, IH) , 7.89 (t, IH) , 7.86 (d, IH) , 7.65 ( , 4H) , 7.54 (s, IH) , 7.52 (dd, IH) ppm. MS (ES+) : m/e= 338.11 (M+H); HPLC-Method A, HPLC- Method D, Rt 2.91 min.
Example 412 (Iff-Indazol-3-yl) - [2- (2-trifluoromethylphenyl) -quinolin-4-yl] -amine (V-7) : XH NMR (500 MHz, d6- DMSO) δ 12.68 (s, IH) , 9.51 (s, IH) , 8.7 (d, IH) , 7.95- 7.89 (m, 2H) , 7.83-7.70 (m, 3H) , 7.68-7.62 (m, 2H) , 7.60 (s, IH) , 7.55-7.52 (m, IH) , 7.49-7.45 (m, IH) , 7.40-7.37 ( , IH) , 7.12-7.09 ( , IH) ; LC-MS (ES+) m/e= 405.15 (M+H); HPLC-Method D Rt 2.25 min.
Example 413 (5, 7-Difluoro-Iff-indazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -quinolin-4-yl] -amine (V-8) : XH NMR
(500 MHz, dg-DMSO) δ 13.31 (s, IH) , 9.49 (s, IH) , 8.70- 8.67 (m, IH) , 7.96-7.92 (m, IH) , 7.85-7.66 (m, 7H) , 7.63- 7.60 (m, IH) , 7.42-7.40 (m, IH) . LC-MS (ES+) m/e= 441.18 (M+H); HPLC-Method D Rt 2.39 min.
Example 414 [2- (2-trifluoromethyl-phenyl) -quinolin-4-yl] - (lff-pyrazolo[4,3-b]pyridin-3-yl) -amine (V-9) : XH NMR (500 MHz, DMS0-d6) δ 13.6 (s, IH) , 11.6 (s, br, IH) , 8.98 (d, IH) , 8.57 (dd, IH) , 8.12 (m, 3H) , 7.97 (m, 2H) , 7.86 (m, , 3H) , 7.49 (dd, IH) , 7.23 (s, IH) ppm. MS (ES+) : m/e= 406.20 (M+H); HPLC-Method A Rt 2.91 min.
Example 415 (2-Phenyl-quinazolin-4-yl) - (2ff- [1,2,4] riazol-3-yl) -amine (IX-154): off-white solid, mp 266-267°C; XH NMR (DMSO) δ 7.50-7.70 (4H, m) , 7.85-8.00 (2H, m) , 8.15-8.25 (2H, m) , 8.37-8.45 (2H, m) , 8.58 (IH, d) , 13.90 (IH, br s) ; IR (solid) 3344, 3059, 1630, 1609, 1570, 1557, 1543, 1501, 1495, 1445, 1411, 1355, 1326, 1267, 1182, 1053, 1038, 760, 676, 667, 654; MS 289.2 (M+H) + .
Example 416 (5-Methyl-2ff- [1, 2,4] triazol-3-yl) - (2 -phenyl- quinazolin-4-yl) -amine (IX-155): XH NMR (500 MHz, DMSO- d6) δ8.59 (s, IH) , 8.42 (d, J = 6.7 Hz, 2H) , 7.79 (m, 4H) , 8.03 (m, 2H) , 7.74 ( , 4H) , 2.51 (s, 3H) ppm. MS (ES+) : m/e= 303.08 (M+H); HPLC-Method A, Rt 2.64 min.
Example 417 (2ff- [1,2,4] -Triazol-3-yl) - [2- (2- trifluoromethylphenyl) -quinazolin-4-yl] -amine (IX-47) :
Pale yellow solid (52% yield) . XH NMR (500 MHz, DMS0-d6) δ8.54 (s, IH) , 8.15 (s, br, IH) , 7.91 (t, IH) , 7.85 (m, 2H) , 7.76 (m, 3H) , 7.66 (t, IH) ppm. MS (ES+) : m/e=
357.13 (M+H); (ES-): m/e= 355.15 (M-H); HPLC-Method A, Rt 2.81 min.
Example 418 (5-Methyl-2ff- [1,2,4] triazol-3-yl) - [2- (2- trifluoromethylphenyl) -quinazolin-4-yl] -amine (IX-38) :
Pale yellow solid (54% yield) . XH NMR (500 MHz, DMS0-d6) δ8.44 (s, br, IH) , 7.92 (m, 3H) , 7.84 (m, IH) , 7.77 (m, 2H) , 7.68 (t, IH) , 2.28 (s, 3H) ppm. MS (ES+) : m/e=
371.14 (M+H); (ES-): m/e= 369.18 (M-H); HPLC-Method A, Rt 2.89 min.
Example 419 (5-Methylsulfanyl-2ff- [1,2, 4] triazol-3-yl) - [2- (2 -trifluoromethylphenyl) -quinazolin-4-yl] -amine (IX- 156) : Pale yellow solid (65% yield) . XH NMR (500 MHz, DMSO-d6) δ8.56 (br, IH) , 7.90 (t, IH) , 7.84 (m, 2H) , 7.78 (m, 2H) , 7.67 (m, 2H) , 2.51 (s, 3H, buried by DMSO) ppm. MS (ES+) : m/e= 403.12 (M+H); (ES-): m/e= 401.16 (M-H) ; HPLC-Method A, Rt 3.20 min.
■Example 420 (Iff- [1, 2,4] Triazol-3-yl) - [3- (2- trifluoromethyl-phenyl) -isoquinolin-1-yl] -amine (IX-175) : A solution of l-chloro-3- (2-trifluoromethyl-phenyl) - isoquinoline (0.326 mmol) and Iff- [1, 2, 4] triazol-3-ylamine (0.651 mmol) in ethanol (3 mL) was heated at 160°C and the solvent evaporated with a stream of nitrogen. The remaining oil was then heated at 160 °C for 18 hours under nitrogen. The resulting melt was dissolved in 5% methanol/dichloromethane (50 mL) , washed with saturated aqueous sodium bicarbonate (1 x 25 mL) then dried over magnesium sulfate. Purification by silica gel chromatography afforded IX-175 as a colorless oil (4% yield). XH NMR (500 MHz, CDC13) δ 9.18 (d, IH) , 8.82 (s, IH) , 7.90 (d, IH) , 7.85-7.75 (m, 3H) , 7.71-7.62 (m, 3H) , 7.60-7.55 (m, 2H) , 4.42-4.35 (m, IH) . LC-MS (ES+) 356.16 (M+H); HPLC-Method D, Rt 3.55 min.
Example 421 (2-Phenyl-quinolin-4-yl) - (Iff- [1,2,4] triazol- 3-yl) -amine (IX-176) : Pale yellow solid (30% yield). XH NMR (500 MHz, d6-DMSO) δ 13.82 (s, IH) , 9.91 (s, IH) , 8.80 (s, IH) , 8.70-8.65 (m, 1H),..8.55 (s, IH) , 8.15-8.12 (m, 2H) , 8.03-7.98 (m, IH) , 7.75-7.72 (m, IH) , 7.57-7.49 (m, 3H) . LC-MS (ES+) m/e= 288.11 (M+H); HPLC-Method D, Rt 1.55 min.
Example 422 (Iff- [1, 2, 4] triazol-3-yl) - [2- (2- trifluoromethyl-phenyl) -quinolin-4-yl] -amine (IX-177) :
Pale yellow solid (46% yield) . XH NMR (500 MHz, d6-DMSO) δ 13.70 (s, IH) , 9.98 (s, IH) , 8.70 (d, IH) , 8.49 (s, IH) , 8.30 (s, IH) , 7.94-7.88 (m, 2H) , 7.80-7.68 (m, 3H) , 7.64-7.56 (m, 2H) . LC-MS (ES+) m/e= 356.18 (M+H); HPLC- Method D, Rt 1.68 min.
Example 423 (l-H-Indazol-3-yl) - [5-methyl-6-morpholin-4- yl-2- (2 -trifluoromethyl-phenyl) -pyrimidin-4-yl] -amine (11-251) : Colorless film; 2 % yield; XH-NMR (500 MHz,
CD3OD) δ 7.84 (m, 2H) , 7.71 (m, 3H) , 7.41 (t, 2H) , 7.14 (m, IH) , 3.74 (m, 4H) , 3.69 (m, 4H) , 1.24 (s, 3H) ppm; HPLC-Method A Rt 3.26 min; MS (FIA) 455.1 (M+H). BIOLOGICAL TESTING The activity of the compounds as protein kinase inhibitors may be assayed in vitro, in vivo or in a cell line. In vitro assays include assays that determine inhibition of either the phosphorylation activity or ATPase activity of the activated protein kinase. Alternate in vi tro assays quantitate the ability of the inhibitor to bind to the protein kinase. Inhibitor binding may be measured by radiolabelling the inhibitor prior to binding, isolating the inhibitor/protein kinase complex and determining the amount of radiolabel bound. Alternatively, inhibitor binding, may be determined by running a competition experiment where new inhibitors are incubated with the protein kinase bound to known radioligands .
BIOLOGICAL TESTING EXAMPLE 1 K± DETERMINATION FOR THE INHIBITION OF GSK-3 Compounds were screened for their ability to inhibit GSK-3β (AA 1-420) activity using a standard coupled enzyme system (Fox et al . (1998) Protein Sci . 1 , 2249) . Reactions were carried out in a solution containing 100 mM HEPES (pH 7.5), 10 mM MgCl2, 25 mM NaCl, 300 μM NADH, 1 mM DTT and 1.5% DMSO. Final substrate concentrations in the assay were 20 μM ATP (Sigma Chemicals, St Louis, MO) and 300 μM peptide (HSSPHQS (P03H2)EDEEE, American Peptide, Sunnyvale, CA) .
Reactions were carried out at 30 °C and 20 nM GSK-3β. Final concentrations of the components of the coupled enzyme system were 2.5 mM phosphoenolpyruvate, 300 μM NADH, 30 μg/ml pyruvate kinase and 10 μg/ml lactate dehydrogenase . An assay stock buffer solution was prepared containing all of the reagents listed, above with the exception of ATP and the test compound of interest. The assay stock buffer solution (175 μl) was incubated in a 5 96 well plate with 5 μl of the test compound of interest at final concentrations spanning 0.002 μM to 30 μM at 30 °C for 10 min. Typically, a 12 point titration was conducted by preparing serial dilutions (from 10 mM compound stocks) with DMSO of the test compounds in
10 daughter plates . The reaction was initiated by the addition of 20 μl of ATP (final concentration 20 μM) . Rates of reaction were obtained using a Molecular Devices Spectramax plate reader (Sunnyvale, CA) over 10 min at 30 °C . The Ki values were determined from the rate data as a
15 function of inhibitor concentration.
The following compounds were shown to have Ki values less than 0.1 μM for GSK-3: compounds II-l, II- 105, 11-33, 11-34, 11-36, 11-39, 11-38, 11-39, 11-40, II- 41, 11-42, 11-46, 11-57, 11-59, 11-60, 11-61, 11-62, II-
20 63, 11-64, 11-66, 11-67, 11-69, 11-70, 11-53, 11-71, II- 99, 11-73, 11-74, 11-75, 11-76, 11-77, II-7, II-8, II-9, 11-10, 11-24, 11-19, 11-78, 11-54, 11-79, 11-80, 11-81, 11-82, 11-83, 11-84, 11-56, 11-86, 11-20, 11-25, 11-26, 11-85, II-21-, 11-27, 11-28, 11-87, 11-88, 11-29, 11-11,
25. 11-12, 11-30, 11-31, 11-13, 11-14, 11-15, 11-16, 11-17, 11-18, 11-79, 11-23, II-2, 11-90, 11-91, 11-92, 11-93, II-3, II-4, II-5, II-6, 11-94, 11-95, 11-96, 11-107, II- 108, 11-109, 11-110, 11-124, 11-125, 11-111, 11-112, II- 113, 11-114, II-115, 11-116, 11-117, 11-118, 11-119, II-
30 120, 11-121, 11-208, III-8, III-7, III-9, 111-37, 111-38, 111-39, 111-40, 111-42, 111-45, 111-46, 111-47, 111-48, III-49, 111-51, 111-52, 111-53, 111-54, 111-55, 111-56, 111-57, 111-58, 111-59, 111-60, 111-61, 111-62, 111-63, 111-30, 111-65, 111-66, 111-67, 111-70, 111-73, 111-31, 111-75, 111-76, 111-77, 111-33, 111-34, III-106, III-108, III-109, III-lll, 111-35, III-116, III-117, III-118, III- 119, III-120, III-121, III-127, III-128, III-141, III- 130, III-131, IV-15, IV-16, IV-17, IV-20, IV-25, IV-26, IV-30, IV-34, V-3, and IX-47.
The following compounds were shown to have Ki values between 0.1 and 1.0 μM for GSK-3: compounds II- 103, 11-104, 11-35, 11-44, 11-45, 11-49, 11-50, 11-97, 11-101, 11-22, 11-32, 111-41, 111-43, 111-44, 111-28,
111-50, 111-29, 111-64, 111-71, 111-74, 111-78, 111-82, 111-88, 111-90, III-102, III-105, III-107, III-110, III- 112, III-114, III-115, III-122, III-124, III-124, IV-1, III-l, III-138, III-140, III-142, III-129, III-132, III- 134, III-135, III-136, IV-1, IV-10, IV-11, IV-12, IV-13, IV-14, IV-19, IV-21, IV-22, IV-23, IV-24, IV-3, IV-4, IV-
6, IV-7, IV-8, IV-29, IV-31, IV-32, IV-33, IV-36, V-2, V-
7, IX-38, IX-154, and IX-177.
The following compounds were shown to have Ki values between 1.0 and 20 μM for GSK-3: compounds 11-43, 11-65, 11-48, 11-47, 11-51, 11-68, 11-52, 11-72, 11-100, 11-98, 11-89, 111-68, 111-81, 111-83, 111-91, 111-94, 111-95, 111-96, 111-97, 111-98, 111-99, III-100, III-101, III-103, III-123, III-137, III-139, III-143, III-145, III-146, V-4, V-8, IX-156, and IX-176.
BIOLOGICAL TESTING EXAMPLE 2 KT DETERMINATION FOR THE INHIBITION OF AURORA-2
Compounds were screened in the following manner for their ability to inhibit Aurora-2 using a standard coupled enzyme assay (Fox et al (1998) Protein Sci 7, 2249) . To an assay stock buffer solution containing 0.1M HEPES 7.5, 10 mM MgCl2, 1 mM DTT, 25 mM NaCl, 2.5 mM phosphoenolpyruvate, 300 mM NADH, 30 mg/ml pyruvate kinase, 10 mg/ml lactate dehydrogenase, 40 mM ATP, and 800 μM peptide (LRRASLG, American Peptide, Sunnyvale, CA) was added a DMSO solution of a compound of the present invention to a final concentration of 30 μM. The resulting mixture was incubated at 30 C for 10 min. The reaction was initiated by the addition of 10 μL of Aurora-2 stock solution to give a final concentration of 70 nM in the assay. The rates of reaction were obtained by monitoring absorbance at 340 nm over a 5 minute read time at 30 °C using a BioRad Ultramark plate reader (Hercules, CA) . The Ki values were determined from the rate data as a function of inhibitor concentration.
The following compounds were shown to have Ki values less than 0.1 μM for Aurora-2: compounds 11-33, 11-34, 11-36, 11-37, 11-40, 11-41, 11-55, III-7, III-9, 111-37, 111-38, 111-39, 111-40, 111-41, 111-42, 111-44, 111-45, 111-46, 111-47, 111-48, 111-49, 111-50, 111-51, 111-52, 111-53, 111-54, 111-55, 111-56, 111-57, 111-59, 111-60, 111-61, 111-63, 111-30, 111-65, 111-66, 111-67, 111-70, 111-31, 111-76, 111-77, 111-78, 111-80, 111-32, 111-33, 111-34, III-106, III-108, III-109, III-110, III- 111, III-112, III-114, 111-35, III-115, III-116, III-117, III-118, III-119, III-120, III-121, IV-7, IV-30, IV-32, and IV-34.
The following compounds were shown to have Ki values between 0.1 and 1.0 μM for Aurora-2: compounds II- 1, 11-105, 11-35, 11-38, 11-39, 11-42, 11-64, 11-70, II- 53, 11-99, 11-77, 11-79, 11-86, 11-20, 11-93, 11-94, III- 28, 111-58, 111-64, 111-71, 111-73, 111-74, 111-75, III- 102 , III - 105 , III - 107 , III - 113 , III - 124 , III - l , III - 130 , IV- 1 , IV- 3 , IV-4 , IV- 6 , IV- 29 , IV- 33 , and V-4 .
The following compounds were shown to have Ki values between 1.0 and 20 μM for Aurora-2: compounds II- 103, 11-104, 11-57, 11-59, 11-61, 11-63,- 11-67, 11-69, 11-75, 11-76, 11-10, 11-19, 11-78, 11-54, 11-80, 11-82, 11-21, 11-90, 11-91, 11-96, 11-107, 111-68, 111-79, III- 82, III-101, III-103, III-127, III-141, III-129, III-132, IV-31, V-2, IX-47, IX-154, and IX-177.
BIOLOGICAL TESTING EXAMPLE 3 CDK-2 INHIBITION ASSAY ' Compounds were screened in the following manner for their ability to inhibit CDK-2 using a standard coupled enzyme assay (Fox et al (1998) Protein Sci 7, 2249) .
To an assay stock buffer solution containing 0.1M HEPES 7.5, 10 mM MgCl2, 1 mM DTT, 25 mM NaCl, 2.5 mM phosphoenolpyruvate, 300 mM NADH, 30 mg/ml pyruvate kinase, 10 mg/ml lactate dehydrogenase, 100 mM ATP, and 100 μM peptide (MAHHHRSPRKRAKKK, American Peptide, Sunnyvale, CA) was added a DMSO solution of a compound of the present invention to a final concentration of 30 μM. The resulting mixture was incubated at 30 °C for 10 min. The reaction was initiated by the addition of
10 μL of CDK-2/Cyclin A stock solution to give a final concentration of 25 nM in the assay. The rates of reaction were obtained by monitoring absorbance at 340 nm over a 5-minute read time at 30 °C using a BioRad Ultramark plate reader (Hercules, CA) . The Ki values were determined from the rate data as a function of inhibitor concentration. BIOLOGICAL TESTING EXAMPLE 4 ERK INHIBITION ASSAY Compounds were assayed for the inhibition of ERK2 by a spectrophotometric coupled-enzyme assay (Fox et al (1998) Protein Sci 7, 2249) . In this assay, a fixed concentration of activated ERK2 (10 nM) was incubated with various concentrations of the compound in DMSO (2.5
%) for 10 min. at 30°C in 0.1 M HEPES buffer, pH 7.5, containing 10 mM MgCl2, 2.5 mM phosphoenolpyruvate, 200 μM NADH, 150 μg/mL pyruvate kinase, 50 μg/mL lactate dehydrogenase, and 200 μM erktide peptide. The reaction was initiated by the addition of 65 μM ATP. The rate of decrease of absorbance at 340 nM was monitored. The IC50 was evaluated from the rate data as a function of inhibitor concentration.
The following compounds were shown to have a Ki value of <lμM for ERK-2: IH-10'9, III-lll, III-115, III- 117, III-118, III-120, and IV-4.
The following compounds were shown to have a Ki value of between lμM and 12μM for ERK-2: III-63, 111-40, and III-108.
BIOLOGICAL TESTING EXAMPLE 5 AKT INHIBITION ASSAY Compounds were screened for their ability to inhibit AKT using a standard coupled enzyme assay (Fox et al., Protein Sci., (1998) 7, 2249). Assays were carried out in a mixture of 100 mM HEPES 7.5, 10 mM MgCl2, 25 mM NaCl , 1 mM DTT and 1.5% DMSO. Final substrate concentrations in the assay were 170 μM ATP (Sigma
Chemicals) and 200 μM peptide (RPRAATF, American Peptide, Sunnyvale, CA) . Assays were carried out at 30 . C and 45 nM AKT. Final concentrations of the components of the coupled enzyme system were 2.5 mM phosphoenolpyruvate, 300 μM NADH, 30 μg/ML pyruvate kinase and 10 μg/ml lactate dehydrogenase.
An assay stock buffer solution was prepared containing all of the reagents listed above, with the exception of AKT, DTT, and the test compound of interest. 56 μl of the- stock solution was placed in a 384 well plate followed by addition of 1 μl of 2 mM DMSO stock containing the test compound (final compound concentration 30 μM) . The plate was preincubated for about 10 minutes at 30 C and the reaction initiated by addition of 10 μl of enzyme (final concentration 45 nM) and 1 mM DTT. Rates of reaction were obtained using a BioRad Ultramark plate reader (Hercules, CA) over a 5* minute read time at 30 C. Compounds showing greater than 50% inhibition versus standard wells containing the assay mixture and DMSO without test compound were titrated to determine IC50 values .
BIOLOGICAL TESTING EXAMPLE 6 SRC INHIBITION ASSAY
The compounds were evaluated as inhibitors of human Src kinase using either a radioactivity-based assay or spectrophotometric assay.
Src Inhibition Assay A: Radioactivity-based Assay The compounds were assayed as inhibitors of full length recombinant human Src kinase (from Upstate Biotechnology, cat. no. 14-117) expressed and purified from baculo viral cells. Src kinase activity was monitored by following the incorporation of 33P from ATP into the tyrosine of a random poly Glu-Tyr polymer substrate of composition, Glu:Tyr = 4:1 (Sigma, cat. no. P-0275) . The following were the final concentrations of the assay components: 0.05 M HEPES, pH 7.6, 10 mM MgCl2, 2 mM DTT, 0.25 mg/ml BSA, 10 μM ATP (1-2 μCi 33P-ATP per reaction) , 5 mg/ml poly Glu-Tyr, and 1-2 units of recombinant human Src kinase. In a typical assay, all the reaction components with the exception of ATP were pre-mixed and aliquoted into assay plate wells.
Inhibitors dissolved in DMSO were added to the wells to give a final DMSO concentration of 2.5%. The assay plate was incubated at 30 °C for 10 min before initiating the reaction with 33P-ATP. After 20 min of reaction, the reactions were quenched with 150 μl of 10% trichloroacetic acid (TCA) containing 20 mM Na3P0. The quenched samples were then transferred to a 96-well filter plate (Whatman, UNI-Filter GF/F Glass Fiber Filter, cat no. 7700-3310) installed on a filter plate vacuum manifold. Filter plates were washed four times with 10% TCA containing 20 mM Na3P0 and then 4 times with methanol. 200μl of scintillation fluid was then added to each well . The plates were sealed and the amount of radioactivity associated with the filters was quantified on a TopCount scintillation counter. The radioactivity incorporated was plotted as a function of the inhibitor concentration. The data was fitted to a competitive inhibition kinetics model to get the i for the compound.
Src Inhibition Assay B: Spectrophotometric Assay The ADP produced from ATP by the human recombinant Src kinase-catalyzed phosphorylation of poly Glu-Tyr substrate was quanitified using a coupled enzyme assay (Fox et al (1998) Protein Sci 7, 2249) . In this assay one molecule of NADH is oxidised to NAD for every molecule of ADP produced in the kinase reaction. The disappearance of NADH can be conveniently followed at 340 nm. The following were the final concentrations of the assay components: 0.025 M HEPES, pH 7.6, 10 mM MgCl2, 2 mM DTT, 0.25 mg/ml poly Glu-Tyr, and 25 nM of recombinant human Src kinase. Final concentrations of the components of the coupled enzyme system were 2.5 mM phosphoenolpyruvate, 200 μM NADH, 30 μg/ml pyruvate kinase and 10 μg/ml lactate dehydrogenase.
In a typical assay, all the reaction components with the exception of ATP were pre-mixed and aliquoted into assay plate wells. Inhibitors dissolved in DMSO were added to the wells to give a final DMSO concentration of 2.5%. The assay plate was incubated at 30 C for 10 min before initiating the reaction with 100 μM ATP. The absorbance change at 340 nm with time, the rate of the reaction, was monitored on a molecular devices plate reader. The data of rate as a function of the inhibitor concentration was fitted to compettive inhibition kinetics model to get the Ki for the compound.
The following compounds were shown to have a K value of <100nM on SRC: 111-31, 111-32, 111-33, 111-34, .111-35, 111-47, 111-65, 111-66, 111-37, 111-38, 111-39, 111-40, 111-42, 111-44, 111-48,. 111-49, 111-70, 111-45, 111-78, 111-76, and IV- 32.
The following compounds were shown to have a Ki value of between lOOnM and lμM for SRC: 111-63, 111-71, 111-75, 111-73, 111-72, 111-74, 111-80, 111-50, IV-30.
The following compounds were shown to have a Ki value of between lμM and 6μM for SRC: III-79, IV-1, and IV-31. While we have hereinbefore presented a number of embodiments of this invention, it is apparent that our basic construction can be altered to provide other embodiments which utilize the compounds and methods of this invention. Therefore, it will be appreciated that the scope of this invention is to be defined by the appended claims rather than by the specific embodiments which have been represented by way of example.

Claims (34)

  1. We claim:
    A compound of formula II :
    II or a pharmaceutically acceptable derivative or prodrug thereof, wherein;
    Ring C is selected from a phenyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, or 1, 2, 4-triazinyl ring, wherein said Ring C has one or two ortho substituents independently selected from -Rx, any substitutable non- ortho carbon position on Ring C is independently substituted by -R5, and two adjacent substituents on Ring C are optionally taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-6 membered ring having 0-3 heteroatoms selected from oxygen, sulfur or nitrogen, said fused ring being optionally substituted by halo, oxo, or -R8;
    R1 is selected from -halo, -CN, -N02, T-V-R6, phenyl, 5-6 membered heteroaryl ring, 5-6 membered heterocyclyl ring, or Cι_6 aliphatic group, said phenyl, heteroaryl, and heterocyclyl rings each optionally substituted by up to three groups independently selected from halo, oxo, or -R8, said Cι-6 aliphatic group optionally substituted with halo, cyano, nitro, or oxygen, or R1 and an adjacent substituent taken together with their intervening atoms form said ring fused to Ring C;
    Rx and Rγ are independently selected from T-R3, or Rx and Rγ are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-8 membered ring having 0-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen, wherein any substitutable carbon on said fused ring formed by Rx and Rγ is substituted by oxo or T-R3, and any substitutable nitrogen on said ring formed by Rx and Ry is substituted by R4;
    T is a valence bond or a Cι-4 alkylidene chain;
    R2 and R2' are independently selected from -R, -T-w-Rs, or R2 and R2' are taken together with their intervening atoms to form a fused, 5-8 membered, unsaturated or partially unsaturated, ring having 0-3 ring heteroatoms selected from nitrogen, oxygen, or sulfur, wherein each substitutable carbon on said fused ring formed by R2 and R2' is substituted by halo, oxo, -CN, -N02, -R7, or -V-Rs, and any substitutable nitrogen on said ring formed by R2 and R2' is substituted by R4;
    R3 is selected from -R, -halo, -OR, -C(=0)R, -C02R, -COCOR, -COCH2COR, -N02, -CN, -S(0)R, -S(0)2R, -SR, -N(R4)2, -CON(R7)2, -S02N(R7)2, -0C(=0)R, -N(R7)COR, -N(R7)C02(C1-5 aliphatic) , -N(R4)N(R4) 2, -C=NN(R4)2, -C=N-OR, -N(R7)CON(R7)2, -N(R7) S02N(R7) _ , -N(R4)S02R, or -OC(=0) N(R)2; each R is independently selected from hydrogen or an optionally substituted group selected from Cι-6 aliphatic, Cs.10 aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms ; each R4 is independently selected from -R7, -COR7,
    -C02 (optionally substituted Cι-S aliphatic) , -CON(R7)2, or -S02R7, or two R4 on the same nitrogen are taken together to form a 5-8 membered heterocyclyl or heteroaryl ring; each R5 is independently selected from -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -CON(R4)2, -S02N(R4)2, -OC(=0)R, -N(R4)COR, -N(R4) C02 (optionally substituted Cι-ε aliphatic) , -N(R4)N(R4)2, -C=NN(R)2, -C=N-OR, -N (R4) CON (R4) 2, -N(R4)S02N(R4)2, -N(R4)S02R, or -OC (=0) N(R4) 2, or R5 and an adjacent substituent taken together with their intervening atoms form said ring fused to Ring C;
    V is -0-, -S-, -SO-, -S02-, -N(R6)S02-, -S02N(R6)-, -N(R6)-, -CO-, -C02-, -N(Rs)CO-, -N (R6) C (O) O- , -N(Rs)CON(Re) -, -N(R6)S02N(R6) -, -N (R6) N (R6) - , -C(0)N(R6)-, -OC(0)N(Re)-, -C(R6)20-, -C(R6)2S-, -C(R6)2S0-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C (R6) 2N(R6) - , -C(Re)2N(R6)C(0)-, -C(R6)2N(R6)C(0)0-, -C (R6) =NN(R6) - , -C(R6)=N-0-, -C(R6)2N(R6)N(R6) -, -C (R6) 2N (R6) S02N (R6) - , or -C(R6)2N(Re)CON(R6) -;
    W is -C(Rs)20-, -C(R6)2S-, -C(Rδ)2S0-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C(RS)2N(RS)-, -CO-, -C02-, -C(R6)OC(0) -, -C(R6)OC(0)N(R6) -, -C (R6) 2N (Rβ) CO- , -C(R6)2N(R6)C(0)0-, -C(R6)=NN(RS) -, -C(R6)=N-0-, -C(Re)2N(R6)N(Re)-, -C(R6)2N(R6)S02N(R6) -, -C(R6)2N(R6)CON(R6) -, or -CON(R6)-; each R6 is independently selected from hydrogen or an optionally substituted Cχ.4 aliphatic group, or two R6 groups on the same nitrogen atom are taken together with the nitrogen atom to form a 5-6 membered heterocyclyl or heteroaryl ring; each R7 is independently selected from hydrogen or an optionally substituted Cι-6 aliphatic group, or two R7 on the same nitrogen are taken together with the nitrogen to form a 5-8 membered heterocyclyl or heteroaryl ring,- and each R8 is independently selected from an optionally substituted Cι-4 aliphatic group, -OR6, -SR6, -COR6, -S02R6, -N(R6)2, -N(R6)N(R6)2, -CN, -N02, -CON(R6)2, or -C02R6.
  2. 2. The compound according to claim 1, wherein said compound has one or more features selected from the group consisting of:
    (a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is selected from an optionally substituted naphthyl, quinolinyl or isoquinolinyl ring;
    (b) Rx is hydrogen or C_.4 aliphatic and Ry is T-R3, or Rx and Rγ are taken together with their intervening atoms to form an optionally substituted 5-7 membered unsaturated or partially unsaturated ring having 0-2 ring nitrogens;
    (c) R is -halo, an optionally substituted Cχ-e aliphatic group, phenyl, -COR6, -OR6, -CN, -S02R6, -S02NH2, -N(R6)2, -C02R6, -CONH2, -NHCOR6, -OC(0)NH2, or -NHS02R6; and
    (d) R2' is hydrogen and R2 is hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a Cι-6 aliphatic group, or R2 and R2' are taken together with their intervening atoms to form a substituted or unsubstituted benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring.
  3. 3. The compound according to claim 2, wherein:
    (a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is selected from an optionally substituted naphthyl, quinolinyl or isoquinolinyl ring;
    (b) Rx is hydrogen or Cχ.4 aliphatic and Rγ is T-R3, or Rx and Rγ are taken together with their intervening atoms to form an optionally substituted 5-7 membered unsaturated or partially unsaturated ring having 0-2 ring nitrogens;
    (c) R1 is -halo, an optionally substituted Cι_6 aliphatic group, phenyl, -COR6, -OR6, -CN, -S02Re, -S02NH2, -N(R6)2, -C02R6, -C0NH2, -NHCOR6, -OC(0)NH2, or -NHS02R6; and
    (d) R2' is hydrogen and R2 is hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a Cι_6 aliphatic group, or R2 and R2' are taken together with their intervening atoms to form a substituted or unsubstituted benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring.
  4. 4. The compound according to claim 2 , wherein said compound has one or more features selected from the group consisting of:
    (a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is selected from an optionally substituted naphthyl ring;
    (b) Rx is hydrogen or methyl and Rγ is -R, N(R4)2, or -OR, or Rx and Ry are taken together with their intervening atoms to form a 5-7 membered unsaturated or partially unsaturated carbocyclo ring optionally substituted with -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02/ -CN, -S(0)R, -S02R, -SR, -N(R4)2/ -CON(R4)2, -S02N(R4)2, -OC(=0)R, -N(R4)COR, -N (R4) C02 (optionally substituted d-e aliphatic) , -N(R4)N(R4) 2, -C=NN(R4)2, -C=N-OR, -N(R4)CON(R4)2, -N (R4) S02N (R4) 2, -N(R4)S02R, or -OC (=0)N(R4) 2, ;
    (c) Rx is -halo, a Cι-6 haloaliphatic group, a Cι_ s aliphatic group, phenyl, or -CN;
    (d) R2' is hydrogen and R2 is hydrogen or a substituted or unsubstituted group selected from aryl, or a Ci-6 aliphatic group, or R2 and R2' are taken together with their intervening atoms to form a substituted or unsubstituted benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring; and
    (e) each R5 is independently selected from -halo, -CN, -N02, -N(R4)2, optionally substituted Cχ_6 aliphatic group, -OR, -C(0)R, -C02R, -CONH(R4), -N(R4)COR, -S02N(R4)2, and -N(R4)S02R.
  5. 5. The compound according to claim 4, wherein:
    (a) Ring C is a phenyl or pyridinyl ring, optionally substituted by -R5, wherein when Ring C and two adjacent substituents thereon form a bicyclic ring system, the bicyclic ring system is selected from an optionally substituted naphthyl ring;
    (b) Rx is hydrogen or methyl and Rγ is -R, N(R4)2, or -OR, or Rx and Rγ are taken together with their intervening atoms to form a 5-7 membered unsaturated or partially unsaturated carbocyclo ring optionally substituted with -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2/ -CON(R)2/ -S02N(R4)2, -OC(=0)R, -N(R4)COR, -N(R4) C02 (optionally substituted Ci-6 aliphatic) , -N(R4)N(R4) _ , -C=NN(R4)2, -C=N-OR, -N(R4)C0N(R4)2, -N(R4) S02N (R4) 2, -N(R4)S02R, or -OC(=0)N(R4)2/;
    (c) Rx is -halo, a Cα.6 haloaliphatic group, a Cχ-6 aliphatic group, phenyl, or -CN;
    (d) R2' is hydrogen and R2 is hydrogen or a substituted or unsubstituted group selected' from aryl, or a C-6 aliphatic group, or R2 and R2' are taken together with their intervening atoms to form a substituted or unsubstituted benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring; and
    (e) each R5 is independently selected from -halo, -CN, -N02, -N(R)2, optionally substituted Cχ-e aliphatic group, -OR, -C(0)R, -C02R, -C0NH(R4), -N(R4)C0R, -S02N(R)2, and -N(R4)S02R.
  6. 6. The compound according to claim 4, wherein said compound has one or more features selected from the group consisting of:
    (a) Rx is hydrogen or methyl and Rγ is methyl, methoxymethyl , ethyl, cyclopropyl, isopropyl, t-butyl, alkyl- or an optionally substituted group selected from 2-pyridyl, 4-pyridyl, piperidinyl, or phenyl, or Rx and Rγ are taken together with their intervening atoms to form a 6-membered unsaturated or partially unsaturated carbocyclo ring optionally substituted with -halo, -R, -OR, -COR, -C02R, -CON(R4)2, -CN, or -N(R4)2 wherein R is an optionally substituted Cχ-6 aliphatic group; (b) Rx is -halo, a Cι_4 aliphatic group optionally substituted with halogen, or -CN;
    (c) R2 and R2' are taken together with their intervening atoms to form a benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring optionally substituted with -halo, -N(R )2, -Cχ.4 alkyl, -Ci-4 haloalkyl, -N02, -O (Cχ-4 alkyl) , -C02 (C1-4 alkyl) , -CN, -S02(Cχ-4 alkyl) , -S02NH2, -0C(0)NH2, -NH2S02 (Cx-4 alkyl) , -NHC(O) (d-4 alkyl) , -C(0)NH2, or -CO (Cχ-4 alkyl) , wherein the (C-4 alkyl) is a straight, branched, or cyclic alkyl group; and
    (d) each R5 is independently selected from -Cl, -F, -CN, -CF3, -NH2, -NH(Cχ-4 aliphatic), -N(Cχ.4 aliphatic) _ , -0(Cχ_4 aliphatic), Cχ_4 aliphatic, and -C02(Cχ-4 aliphatic).
  7. 7. The compound according to claim 6, wherein:
    (a) Rx is hydrogen or methyl and Rγ is methyl, methoxymethyl , ethyl, cyclopropyl, isopropyl, t-butyl, alkyl- or an optionally substituted group selected from 2-pyridyl, 4-pyridyl, piperidinyl, or phenyl, or Rx and Rγ are taken together with, their intervening atoms to form a benzo ring or a partially unsaturated carbocyclo ring optionally substituted with -halo, -R, -OR, -COR, -C02R, -CON(R)2, -CN, or -N(R )2 wherein R is an optionally substituted Cχ-S aliphatic group;
    (b) Rx is -halo, a Cχ.4 aliphatic group optionally substituted with halogen, or -CN;
    (c) R2 and R2' are taken together with their intervening atoms to form a benzo, pyrido, pyrimido or partially unsaturated 6-membered carbocyclo ring optionally substituted with -halo, -N(R4)2, -Cχ-4 alkyl, -C1-4 haloalkyl, -N02, -O (Cχ-4 alkyl) , -C02 (Cχ-4 alkyl) , -CN, -S02(Cχ-4 alkyl) , -S02NH2, -OC(0)NH2, -NH2S02 (Cχ.4 alkyl) , -NHC(O) (d-4 alkyl) , -C(0)NH2, or -CO (Cχ-4 alkyl) , wherein the (Cχ_4 alkyl) is a straight, branched, or cyclic alkyl group,- and
    (d) each R5 is independently selected from -Cl, -F, -CN, -CF3, -NH2, -NH(Cχ-4 aliphatic) , -N(Cχ-4 aliphatic)2, -0(Cχ-4 aliphatic), Cχ-4 aliphatic, and -C02(Cχ-4 aliphatic).
  8. 8. The compound according to claim 7 , wherein Rx and Rγ are each methyl or R and Rγ are taken together with the pyrimidine ring to form an optionally substituted ring selected from quinazoline or tetrahydroquinazoline, and R2 and R2' are taken together with the pyrazole ring to form an optionally substituted indazole ring.
  9. 9. The compound according to claim 1, wherein said compound is selected from Table 1.
  10. 10. A composition comprising a compound according carrier.
  11. 11. The composition according to claim 10 further comprising a second therapeutic agent . '
  12. 12. A method of inhibiting GSK-3 or Aurora activity in a patient comprising the step of administering to said patient a therapeutically effective amount of the composition according to claim 10.
  13. 13. The method according to claim 12, wherein said method inhibits GSK3 activity in a patient.
  14. 14. A method of inhibiting GSK-3 or Aurora activity in a biological sample comprising contacting said biological with the compound according to claim 1.
  15. 15. A method of treating a disease that is alleviated by treatment with an GSK-3 inhibitor, said method comprising the step of administering to a patient in need of such a treatment a therapeutically effective amount of the composition according to claim 10.
  16. 16. The method according to claim 15 further comprising the step of administering to said patient a second therapeutic agent .
  17. 17. The method according to claim 15, wherein said disease is diabetes .
  18. 18. The method according to claim 15 , wherein said disease is Alzheimer's disease.
  19. 19. The method according to claim 15, wherein said disease is schizophrenia.
  20. 20. A method of enhancing glycogen synthesis in a patient in need thereof, which method comprises the step of administering to said patient a therapeutically effective amount of the composition according to claim 10.
  21. 21. A method of lowering blood levels of glucose in a patient in need thereof, which method comprises the step of administering to said patient a therapeutically effective amount of the composition according to claim 10.
  22. 22. A method of inhibiting the production of hyperphosphorylated Tau protein in a patient in need thereof, which method comprises the step of administering to said patient a therapeutically effective amount of the composition according to claim 10.
  23. 23. A method of inhibiting the phosphorylation of β-catenin in a patient in need thereof, which method comprises the step of administering to said patient a therapeutically effective amount of the composition according to claim 10.
  24. 24. A method of treating a disease that is alleviated by treatment with an aurora inhibitor, which method comprises the step of administering to a patient in need of such a treatment a therapeutically effective amount of the composition according to claim 10.
  25. 25. The method according to claim 24, further comprising the step of administering to said patient a second therapeutic agent .
  26. 26. The method according to claim 24 wherein said disease is cancer.
  27. 27. A compound of formula A:
    wherein Rxo is one to three substituents that are each independently selected from fluoro, bromo, Cχ_6 haloalkyl, nitro, or 1-pyrrolyl.
  28. 28. A compound of formula B:
    B wherein:
    R1 is selected from Cl, F, CF3, CN, or N02;
    R5 is one to three substituents that are each independently selected from H, Cl, F, CF3, N02, or CN, provided that Rx and R5 are not simultaneously Cl;
    Rx and Rγ are independently selected from T-R3, or Rx and Rγ are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-8 membered ring having 0-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen, wherein any substitutable carbon on said fused ring formed by Rx and Rγ is optionally and independently substituted by T-R3, and any substitutable nitrogen on said ring formed by Rx and Rγ is substituted by R4;
    T is a valence bond or a Cχ-4 alkylidene chain;
    R3 is selected from -R, -halo, -OR, -C(=0)R, -C02R, -COCOR, -COCH2COR, -N02, -CN, -S(0)R, -S(0)2R, -SR, -N(R4)2, -C0N(R7)2, -S02N(R7)2, -0C(=0)R, -N(R7)COR, -N(R7) C02 (optionally substituted C_.6 aliphatic) , -N(R4)N(R4)2, -C=NN(R4)2, -C=N-OR, -N(R7) CON (R7) 2, -N(R7)S02N(R7)2, -N(R4)S02R, or -OC (=0)N (R7) 2; each R is independently selected from hydrogen or an optionally substituted group selected from Cχ-e aliphatic, C6-xo aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms ; each R4 is independently selected from -R7, -COR7,
    -C02 (optionally substituted Cχ.6 aliphatic) , -CON(R7)2, or -S02R7, or two R4 on the same nitrogen are taken together to form: a 5-8 membered heterocyclyl or heteroaryl ring; and each R7 is independently selected from hydrogen or an optionally substituted Cχ-6 aliphatic group, or two R7 on the same nitrogen are taken together with the nitrogen to form a 5-8 membered heterocyclyl or heteroaryl ring.
  29. 29. The compound according to claim 28 wherein R1 is
    CF
  30. 30. A compound of formula C:
    C wherein:
    R2 and R2' are independently selected from -R, -T-W-R6, or R2 and R2' are taken together with their intervening atoms to form a fused, 5-8 membered, unsaturated or partially unsaturated, ring having 0-3 ring heteroatoms selected from nitrogen, oxygen, or sulfur, wherein each substitutable carbon on said fused ring formed by R2 and R2' is substituted by halo, oxo, -CN, -N02, -R7ι or -V-R6, and any substitutable nitrogen on said ring formed by R2 and R2' is substituted by R4; Rx and Rγ are independently selected from T-R3, or Rx and Rγ are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-8 membered ring having 0-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen, wherein any substitutable carbon on said fused ring formed by Rx and Rγ is optionally and independently substituted by T-R3, and any substitutable nitrogen on said ring formed by Rx and Rγ is substituted by R4,-
    T is a valence bond or a Cχ-4 alkylidene chai ,-
    V is -0-, -S-, -SO-, -S02-, -N(R6)S02-, -S02N(R6)-, -N(R6)-, -CO-, -C02-, -N(Re)CO-, -N (Rδ) C (O) O- , -N(R6)CON(Rs) -, -N(R6)S02N(R6) -, -N(R6)N (R6) - , -C(0)N(R6)-, -OC(0)N(R6)-, -C(R6)20-, -C(R6)2S-, -C(R6)2S0-, -C(Rs)2S02-, -C(R6)2S02N(R6)-, -C (R6) 2N (R6) - , -C(Rs)2N(R6)C(0) -, -C(Rδ)2N(R6)C(0)0-, -C (R6) =NN(RS) - , -C(R6)=N-0-, -C(R6)2N(R6)N(R6) -, -C (R6) 2N (R6) S02N(R6) - , or -C (R6) 2N (RS) CON (R6) - ;
    W is -C(R6)20-, -C(R6)2S-, -C(Rδ)2SO-, -C(R6)2S02-, -C(R6)2S02N(R6)-, -C(R6)2N(R6)-, -CO-, -C02-, -C(R6)OC(0) -, -C(R6)OC(0)N(R6) -, -C (R6) 2N(R6) CO- , -C(R6)2N(R6)C(0)0-, -C(R6)=NN(R6) -, -C(R6)=N-0-, -C(R6)2N(R6)N(R6) -, -C(Rδ)2N(R6)S02N(Rδ) -, -C(Rδ)2N(Rδ)CON(R6) -, or -CON(R6)-;
    R3 is selected from -R, -halo, -OR, -C(=0)R, -C02R, -COCOR, -COCH2COR, -N02, -CN, -S(0)R, -S(0)2R, -SR, -N(R4)2, -CON(R7)2, -S02N(R7)2, -OC(=0)R, -N(R7)C0R, -N(R7) C02 (optionally substituted Cχ-6 aliphatic) , -N(R4)N(R4)2, -C=NN(R4)2, -C=N-OR, -N (R7) CON (R7) 2, -N(R7)S02N(R7)2, -N(R4)S02R, or -OC (=0) N(R7) _ ; each R is independently selected from hydrogen or an optionally substituted group selected from Qx.6 aliphatic, C6-10 aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms; each R4 is independently selected from -R7, -COR7,
    -C02 (optionally substituted Cι_6 aliphatic) , -CON(R7)2, or -S02R7, or two R4 on the same nitrogen are taken together to form a 5-8 membered heterocyclyl or heteroaryl ring. each Rδ is independently selected from hydrogen or an optionally substituted Cι-4 aliphatic group, or two Rδ groups on the same nitrogen atom are taken together with the nitrogen atom to form a 5-6 membered heterocyclyl or heteroaryl ring; and each R7 is independently selected from hydrogen or an optionally substituted Cι-6 aliphatic group, or two R7 on the same nitrogen are taken together with the nitrogen to form a 5-8 membered heterocyclyl or heteroaryl ring.
  31. 31. The compound according to claim 30, wherein Rx and Ry are each methyl, or Rx and Ry are taken together with the pyrimidine ring to form a quinazoline or tetrahydroquinazoline ring.
  32. 32. The compound according to claim 31, wherein R2 and R2' are taken together with the pyrazole ring to form an indazole ring.
  33. 33. A compound of formula D:
    D wherein: Rx and Rγ are independently selected from T-R3, or Rx and Ry are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-8 membered ring having 0-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen, wherein any substitutable carbon on said fused ring formed by Rx and Rγ is optionally and independently substituted by T-R3, and any substitutable nitrogen on said ring formed by is substituted by R4,-
    T is a valence bond or a Cι-4 alkylidene chain;
    R3 is selected from -R, -halo, -OR, -C(=0)R, -C02R, -COCOR, -COCH2COR, -N02/ -CN, -S(0)R, -S(0)2R, -SR, -N(R4)2, -CON(R7)2, -S02N(R7)2, -OC(=0)R, -N(R7)COR, -N(R7) C02 (optionally substituted Cι-e aliphatic) , -N(R)N(R4)2, -C=NN(R4)2, -C=N-OR, -N(R7) CON(R7) 2, -N(R7)S02N(R7)2, -N(R4)S02R, or -OC (=0)N(R7) 2; each R is independently selected from hydrogen or an optionally substituted group selected from Cι-6 aliphatic, C6_ι0 aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms ,- each R4 is independently selected from -R7, -COR7,
    -C02 (optionally substituted Cι-6 aliphatic) , -C0N(R7)2, or -S02R7, or two R4 on the same nitrogen are taken together to form a 5-8 membered heterocyclyl or heteroaryl ring; and each R5 is independently selected from -R, halo, -OR, -C(=0)R, -C02R, -COCOR, -N02, -CN, -S(0)R, -S02R, -SR, -N(R4)2, -CON(R4)2, -S02N(R4)2, -OC(=0)R, -N(R4)COR, -N(R4) C02 (optionally substituted Cι_6 aliphatic) , -N(R4)N(R4)2, -C=NN(R4)2, -C=N-OR, -N (R4) CON (R4) 2, -N(R4)S02N(R4)2, -N(R4)S02R, or -OC (=0)N(R4) 2.
  34. 34. The compound according to claim 33, wherein Rx and Ry are each methyl, or Rx and Rγ are taken together with the pyrimidine ring to form a quinazoline or tetrahydroquinazoline ring.
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Families Citing this family (394)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2264819C (en) * 1996-09-04 2010-03-23 Intertrust Technologies Corp. Trusted infrastructure support systems, methods and techniques for secure electronic commerce, electronic transactions, commerce process control and automation, distributed computing, and rights management
US6184226B1 (en) * 1998-08-28 2001-02-06 Scios Inc. Quinazoline derivatives as inhibitors of P-38 α
US6982260B1 (en) 1999-11-22 2006-01-03 Warner-Lambert Company Quinazolines and their use for inhibiting cyclin-dependent kinase enzymes
MXPA02006338A (en) 1999-12-24 2002-12-13 Aventis Pharma Ltd Azaindoles.
EP1317449B1 (en) * 2000-09-15 2006-05-31 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
US6660731B2 (en) * 2000-09-15 2003-12-09 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
US7473691B2 (en) * 2000-09-15 2009-01-06 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
JP2004518662A (en) * 2000-12-19 2004-06-24 スミスクライン　ビーチャム　パブリック　リミテッド　カンパニー Pyrazolo [3,4-C] pyridines as GSK-3 inhibitors
ATE430742T1 (en) 2000-12-21 2009-05-15 Smithkline Beecham Corp PYRIMIDINAMINES AS ANGIOGENESIS MODULATORS
ES2265450T3 (en) * 2000-12-21 2007-02-16 Vertex Pharmaceuticals Incorporated PIRAZOL COMPOUNDS USED AS INHIBITORS OF PROTEIN QUINASA.
WO2002079163A1 (en) * 2001-03-30 2002-10-10 Smithkline Beecham Corporation Aminopyridine derivatives as estrogen receptor modulators
JP4316893B2 (en) 2001-05-16 2009-08-19 バーテックス ファーマシューティカルズ インコーポレイテッド Inhibitors of Src and other protein kinases
GB0115109D0 (en) 2001-06-21 2001-08-15 Aventis Pharma Ltd Chemical compounds
US7115617B2 (en) 2001-08-22 2006-10-03 Amgen Inc. Amino-substituted pyrimidinyl derivatives and methods of use
US6939874B2 (en) 2001-08-22 2005-09-06 Amgen Inc. Substituted pyrimidinyl derivatives and methods of use
EP2264014A1 (en) 2001-08-31 2010-12-22 Université Louis Pasteur Substituted pyridazines as anti-inflammatory agents and protein kinase inhibitors
WO2003030909A1 (en) * 2001-09-25 2003-04-17 Bayer Pharmaceuticals Corporation 2- and 4-aminopyrimidines n-substtituded by a bicyclic ring for use as kinase inhibitors in the treatment of cancer
CZ2004359A3 (en) 2001-09-26 2004-09-15 Pharmacia Italia S.P.A. Aminoindazole derivatives exhibiting kinase inhibitor activity, process of their preparation and pharmaceutical compositions in which the derivatives are comprised
TWI330183B (en) * 2001-10-22 2010-09-11 Eisai R&D Man Co Ltd
SE0104140D0 (en) * 2001-12-07 2001-12-07 Astrazeneca Ab Novel Compounds
CA2469316A1 (en) 2001-12-07 2003-06-19 Vertex Pharmaceuticals, Inc. Pyrimidine-based compounds useful as gsk-3 inhibitors
US20030187026A1 (en) 2001-12-13 2003-10-02 Qun Li Kinase inhibitors
AU2002357164A1 (en) 2001-12-17 2003-06-30 Smithkline Beecham Corporation Pyrazolopyridazine derivatives
AU2002361846A1 (en) * 2001-12-21 2003-07-15 Bayer Pharmaceuticals Corporation Quinazoline and quinoline derivative compounds as inhibitors of prolylpeptidase, inducers of apoptosis and cancer treatment agents
US20030158195A1 (en) 2001-12-21 2003-08-21 Cywin Charles L. 1,6 naphthyridines useful as inhibitors of SYK kinase
RS63204A (en) 2002-01-17 2006-10-27 Neurogen Corporation Substituted quinazolin-4-ylamine analogues as modulators of capsaicin
TWI329105B (en) 2002-02-01 2010-08-21 Rigel Pharmaceuticals Inc 2,4-pyrimidinediamine compounds and their uses
AU2003215087B2 (en) * 2002-02-06 2009-07-16 Vertex Pharmaceuticals Incorporated Heteroaryl compounds useful as inhibitors of GSK-3
DE60332433D1 (en) 2002-03-15 2010-06-17 Vertex Pharma AZOLYLAMINOAZINE AS PROTEIN KINASE INHIBITOR
WO2003078426A1 (en) * 2002-03-15 2003-09-25 Vertex Pharmaceuticals, Inc. Azolylaminoazine as inhibitors of protein kinases
DE60332604D1 (en) * 2002-03-15 2010-07-01 Vertex Pharma AZOLYLAMINOAZINE AS PROTEIN KINASE INHIBITOR
RU2004132847A (en) * 2002-04-05 2006-08-20 Берингер Ингельхайм Фарма Гмбх Унд Ко.Кг (De) METHOD FOR TREATING HYPERSECRATION OF SLIMAS
DE60331329D1 (en) 2002-05-01 2010-04-01 Vertex Pharma CRYSTAL STRUCTURE OF THE AURORA-2 PROTEIN AND ITS BINDING POCKETS
ATE493987T1 (en) 2002-05-22 2011-01-15 Amgen Inc AMINOPYRIMIDINE DERIVATIVES FOR USE AS VANILLOID RECEPTOR LIGANDS FOR THE TREATMENT OF PAIN
JPWO2003104230A1 (en) * 2002-06-07 2005-10-06 協和醗酵工業株式会社 Bicyclic pyrimidine derivatives
ES2402855T3 (en) 2002-06-14 2013-05-09 Merck Serono Sa Azol-methylidene cyanide derivatives and their use as protein kinase modulators
MY141867A (en) * 2002-06-20 2010-07-16 Vertex Pharma Substituted pyrimidines useful as protein kinase inhibitors
AU2003249369A1 (en) 2002-06-21 2004-01-06 Cellular Genomics, Inc. Certain amino-substituted monocycles as kinase modulators
DE60320560T2 (en) * 2002-07-17 2008-12-11 Pfizer Italia S.R.L. Heterocyclic pyrazole derivatives as kinase inhibitors
WO2004010929A2 (en) * 2002-07-25 2004-02-05 Scios, Inc. METHODS FOR IMPROVEMENT OF LUNG FUNCTION USING TGF-β INHIBITORS
DK1534286T3 (en) 2002-07-29 2010-04-26 Rigel Pharmaceuticals Inc Methods for treating or preventing autoimmune diseases with 2,4-pyrimidinediamine compounds
ES2273043T3 (en) * 2002-08-02 2007-05-01 Vertex Pharmaceuticals Incorporated PIRAZOL COMPOSITIONS USEFUL AS INHIBITORS OF GSK-3.
SI1532145T1 (en) * 2002-08-02 2007-02-28 Vertex Pharma Pyrazole compositions useful as inhibitors of gsk-3
WO2004014865A1 (en) * 2002-08-13 2004-02-19 Merck Sharp & Dohme Limited Phenylpyridazine derivatives as ligands for gaba receptors
US7304071B2 (en) 2002-08-14 2007-12-04 Vertex Pharmaceuticals Incorporated Protein kinase inhibitors and uses thereof
NZ539193A (en) 2002-09-05 2008-04-30 Aventis Pharma Sa Novel aminoindazole derivatives as medicines and pharmaceutical compositions containing same
FR2844267B1 (en) * 2002-09-05 2008-02-15 Aventis Pharma Sa NOVEL DERIVATIVES OF AMINOINDAZOLES AS MEDICAMENTS AND PHARMACEUTICAL COMPOSITIONS COMPRISING THEM
UA80295C2 (en) 2002-09-06 2007-09-10 Biogen Inc Pyrazolopyridines and using the same
RU2005110656A (en) * 2002-09-10 2006-01-20 Сайос Инк. (Us) TGF INHIBITORS
DE60330895D1 (en) 2002-11-01 2010-02-25 Vertex Pharma COMPOUNDS SUITED AS INHIBITORS OF JAK AND OTHER PROTEIN KINASES
JP2006508107A (en) 2002-11-05 2006-03-09 バーテックス　ファーマシューティカルズ　インコーポレイテッド Compounds useful as inhibitors of JAK and other protein kinases
MXPA05005477A (en) * 2002-11-21 2005-07-25 Chiron Corp 2,4,6-trisubstituted pyrimidines as phosphotidylinositol (pi) 3-kinase inhibitors and their use in the treatment of cancer.
SI2316831T1 (en) * 2002-11-21 2013-07-31 Novartis Ag 2-(morpholin-4-yl)pyrimidines as phosphotidylinositol (PI) 3-kinase inhibitors and their use in the treatment of cancer
EP1571146A4 (en) * 2002-12-10 2010-09-01 Ono Pharmaceutical Co Nitrogen-containing heterocyclic compounds and medicinal use thereof
BR0316606A (en) 2002-12-12 2005-10-11 Aventis Pharma Sa Aminoindazole derivatives and their use as kinase inhibitors
FR2848554A1 (en) * 2002-12-12 2004-06-18 Aventis Pharma Sa New aminoindazole derivatives are kinase inhibitors, useful in the treatment of neurodegenerative diseases, obesity, metabolic disorders, diabetes, hypertension, polycystic ovarian syndrome, cancers and other disorders
EP1569925A1 (en) 2002-12-13 2005-09-07 Neurogen Corporation 2-substituted quinazolin-4-ylamine analogues as capsaicin receptor modulators
US7601718B2 (en) 2003-02-06 2009-10-13 Vertex Pharmaceuticals Incorporated Compositions useful as inhibitors of protein kinases
US7157455B2 (en) * 2003-02-10 2007-01-02 Hoffmann-La Roche Inc. 4-Aminopyrimidine-5-one derivatives
CA2520465A1 (en) * 2003-03-28 2004-10-14 Scios Inc. Bi-cyclic pyrimidine inhibitors of tgf.beta.
US7763627B2 (en) * 2003-04-09 2010-07-27 Exelixis, Inc. Tie-2 modulators and methods of use
CN1809351A (en) * 2003-04-24 2006-07-26 麦克公司 Inhibitors of Akt activity
WO2004096808A1 (en) * 2003-04-28 2004-11-11 De Novo Pharmaceuticals Limited Triazine compounds and their use
WO2005011677A1 (en) * 2003-06-13 2005-02-10 Arena Pharmaceuticals, Inc. 5-substituted 2h-pyrazole-3-carboxylic acid derivatives as agonists for the nicotinic acid receptor rup25 for the treatment of dyslipidemia and related diseases
BRPI0411514A (en) * 2003-06-20 2006-08-01 Coley Pharm Gmbh small molecule toll-like receptor antagonists
TW200510373A (en) 2003-07-14 2005-03-16 Neurogen Corp Substituted quinolin-4-ylamine analogues
US7329664B2 (en) 2003-07-16 2008-02-12 Neurogen Corporation Substituted (7-pyridyl-4-phenylamino-quinazolin-2-yl)-methanol analogues
PL1651612T3 (en) 2003-07-22 2012-09-28 Astex Therapeutics Ltd 3,4-disubstituted 1h-pyrazole compounds and their use as cyclin dependent kinases (cdk) and glycogen synthase kinase-3 (gsk-3) modulators
PT1656372E (en) 2003-07-30 2013-06-27 Rigel Pharmaceuticals Inc 2,4-pyrimidinediamine compounds for use in the treatment or prevention of autoimmune diseases
WO2005014558A1 (en) * 2003-08-05 2005-02-17 Vertex Pharmaceuticals Incorporated Condensed pyramidine compounds as inhibitors of voltage-gated ion channels
WO2005013982A1 (en) * 2003-08-06 2005-02-17 Vertex Pharmaceuticals Incorporated Aminotriazole compounds useful as inhibitors of protein kinases
ATE546452T1 (en) * 2003-09-23 2012-03-15 Vertex Pharma PYRAZOLOPYRROL DERIVATIVES AS PROTEIN KINASE INHIBITORS
GB0323137D0 (en) 2003-10-03 2003-11-05 Chang Lisa C W 2,4,6- Trisubstituted pyrimidines and their different uses
DE602004022187D1 (en) * 2003-10-17 2009-09-03 Astrazeneca Ab 4- (PYRAZOL-3-YLAMINO) PYRIMIDINE DERIVATIVES FOR USE IN THE TREATMENT OF CANCER
US8455489B2 (en) * 2003-11-10 2013-06-04 Exelixis, Inc. Substituted pyrimidine compositions and methods of use
TW200528106A (en) * 2003-11-10 2005-09-01 Synta Pharmaceuticals Corp Pyridine compounds
SI1689715T1 (en) * 2003-12-03 2011-07-29 Ym Biosciences Australia Pty Tubulin inhibitors
WO2005056547A2 (en) * 2003-12-04 2005-06-23 Vertex Pharmaceuticals Incorporated Quinoxalines useful as inhibitors of protein kinases
MXPA06006532A (en) * 2003-12-09 2006-08-23 Vertex Pharma Naphthyridine derivatives and their use as modulators of muscarinic receptors.
JP2007514759A (en) * 2003-12-19 2007-06-07 タケダ サン ディエゴ インコーポレイテッド Kinase inhibitor
TW200530235A (en) 2003-12-24 2005-09-16 Renovis Inc Bicycloheteroarylamine compounds as ion channel ligands and uses thereof
AU2005207946A1 (en) 2004-01-23 2005-08-11 Amgen Inc. Quinoline quinazoline pyridine and pyrimidine counds and their use in the treatment of inflammation angiogenesis and cancer
US7435823B2 (en) 2004-01-23 2008-10-14 Amgen Inc. Compounds and methods of use
WO2005077938A1 (en) * 2004-02-11 2005-08-25 Amgen Inc. Vanilloid receptor ligands and their use in treatments
US7459457B2 (en) 2004-04-13 2008-12-02 Icagen, Inc. Polycyclic pyridines as potassium ion channel modulators
JP2007533753A (en) * 2004-04-23 2007-11-22 タケダ サン ディエゴ インコーポレイテッド Indole derivatives and their use as kinase inhibitors
US7793137B2 (en) 2004-10-07 2010-09-07 Cisco Technology, Inc. Redundant power and data in a wired data telecommunincations network
US7572784B2 (en) 2004-05-14 2009-08-11 Millennium Pharmaceuticals, Inc. Compounds and methods for inhibiting mitotic progression
EP1604988A1 (en) * 2004-05-18 2005-12-14 Sanofi-Aventis Deutschland GmbH Pyridazinone derivatives, methods for producing them and their use as pharmaceuticals
EP1598348A1 (en) 2004-05-18 2005-11-23 Aventis Pharma Deutschland GmbH Novel pyridazinone derivatives as inhibitors of CDK2
DE102004028862A1 (en) * 2004-06-15 2005-12-29 Merck Patent Gmbh 3-aminoindazoles
GB0415364D0 (en) * 2004-07-09 2004-08-11 Astrazeneca Ab Pyrimidine derivatives
US20080261821A1 (en) * 2004-07-21 2008-10-23 The Regents Of Te University Of California Mechanism-Based Crosslinkers
WO2006023931A2 (en) * 2004-08-18 2006-03-02 Takeda San Diego, Inc. Kinase inhibitors
DE602005027081D1 (en) 2004-08-19 2011-05-05 Dsm Ip Assets Bv METHOD FOR THE RECTIFICATION OF VITAMIN E ACETATE
GB0419416D0 (en) 2004-09-01 2004-10-06 Inst Of Ex Botany Ascr 4-Arylazo-3,5-Diamino-Pyrazole compounds and use thereof
CA2579143A1 (en) 2004-09-13 2006-03-23 Amgen Inc. Vanilloid receptor ligands and their use in treatments
AU2005286592A1 (en) * 2004-09-23 2006-03-30 Reddy Us Therapeutics, Inc. Novel pyrimidine compounds, process for their preparation and compositions containing them
AR050948A1 (en) 2004-09-24 2006-12-06 Hoffmann La Roche DERIVATIVES OF FTALAZINONA; ITS OBTAINING AND ITS USE IN THE MANUFACTURE OF MEDICINES FOR THE TREATMENT OF CANCER.
US7285569B2 (en) 2004-09-24 2007-10-23 Hoff Hoffmann-La Roche Inc. Tricycles, their manufacture and use as pharmaceutical agents
AP2007003923A0 (en) 2004-09-30 2007-02-28 Tibotec Pharm Ltd Hcv inhibiting bi-cyclic pyrimidines
TW200621251A (en) 2004-10-12 2006-07-01 Neurogen Corp Substituted biaryl quinolin-4-ylamine analogues
WO2006044687A2 (en) * 2004-10-15 2006-04-27 Takeda San Diego, Inc. Kinase inhibitors
TW200621257A (en) * 2004-10-20 2006-07-01 Astellas Pharma Inc Pyrimidine derivative fused with nonaromatic ring
EP2592075B1 (en) 2004-11-02 2015-04-29 Northwestern University Pyridazine compounds for the treatment of inflammatory diseases
WO2006050359A2 (en) 2004-11-02 2006-05-11 Northwestern University Pyridazine compounds and methods
RU2007122485A (en) 2004-11-17 2008-12-27 Мийкана Терапьютикс KINASE INHIBITORS
US7557207B2 (en) 2004-11-24 2009-07-07 Rigel Pharmaceuticals, Inc. Spiro 2,4-pyrimidinediamine compounds and their uses
ES2450566T3 (en) 2004-11-30 2014-03-25 Amgen Inc. Quinazoline and quinoline analogues and their use as medicines to treat cancer
US20060128710A1 (en) * 2004-12-09 2006-06-15 Chih-Hung Lee Antagonists to the vanilloid receptor subtype 1 (VR1) and uses thereof
EP1831216A2 (en) * 2004-12-23 2007-09-12 Pfizer Products Inc. Heteroaromatic derivatives useful as anticancer agents
CA2590110C (en) * 2004-12-30 2014-06-03 Exelixis, Inc. Kinase modulators and method of use
AU2006206458B2 (en) 2005-01-19 2012-10-25 Rigel Pharmaceuticals, Inc. Prodrugs of 2,4-pyrimidinediamine compounds and their uses
US8404718B2 (en) 2005-01-21 2013-03-26 Astex Therapeutics Limited Combinations of pyrazole kinase inhibitors
AR054425A1 (en) 2005-01-21 2007-06-27 Astex Therapeutics Ltd PIPERIDIN ADDITION SALTS 4-IL-ACID AMID 4- (2,6-DICLORO-BENZOILAMINO) 1H-PIRAZOL-3-CARBOXILICO.
ATE451363T1 (en) * 2005-01-26 2009-12-15 Schering Corp 3-(INDAZOL-5-YL)-(1,2,4)TRIAZINE DERIVATIVES AND RELATED COMPOUNDS AS PROTEIN KINASE INHIBITORS FOR THE TREATMENT OF CANCER
EP1846394B1 (en) * 2005-02-04 2011-10-26 AstraZeneca AB Pyrazolylaminopyridine derivatives useful as kinase inhibitors
US20060178388A1 (en) 2005-02-04 2006-08-10 Wrobleski Stephen T Phenyl-substituted pyrimidine compounds useful as kinase inhibitors
DE602006001515D1 (en) * 2005-02-16 2008-07-31 Astrazeneca Ab CHEMICAL COMPOUNDS
WO2006100461A1 (en) * 2005-03-23 2006-09-28 Astrazeneca Ab 2-AZETIDINYL-4-(lH-PYRAZOL-3-YLAMINO)PYRIMIDINES AS INHIBITORS OF INSULIN-LIKE GROWTH FACTOR-I RECEPTOR ACTIVITY
US7402596B2 (en) 2005-03-24 2008-07-22 Renovis, Inc. Bicycloheteroaryl compounds as P2X7 modulators and uses thereof
WO2006100310A1 (en) 2005-03-25 2006-09-28 Tibotec Pharmaceuticals Ltd Heterobicylic inhibitors of hcv
SI1869032T1 (en) * 2005-04-05 2008-12-31 Astrazeneca Ab Pyrimidine derivatives for use as anticancer agents
GB0507347D0 (en) * 2005-04-12 2005-05-18 Astrazeneca Ab Chemical compounds
JP2008535876A (en) 2005-04-14 2008-09-04 エフ．ホフマン−ラ ロシュ アーゲー Aminopyrazole derivatives, their production and use as pharmaceutical formulations.
JO2787B1 (en) 2005-04-27 2014-03-15 امجين إنك, Substituted Amid derivatives & methods of use
US7928126B2 (en) 2005-04-28 2011-04-19 Mitsubishi Tanabe Pharma Corporation Cyanopyridine derivative and use thereof as medicine
US7745451B2 (en) * 2005-05-04 2010-06-29 Renovis, Inc. Tetrahydronaphthyridine and tetrahydropyrido[4,3-d]pyrimidine compounds and compositions thereof useful in the treatment of conditions associated with neurological and inflammatory disorders and dysfunctions
US20080207594A1 (en) 2005-05-04 2008-08-28 Davelogen Aktiengesellschaft Use of Gsk-3 Inhibitors for Preventing and Treating Pancreatic Autoimmune Disorders
EP1888561A1 (en) * 2005-05-05 2008-02-20 AstraZeneca AB Pyrazolyl-amino- substituted pyrimidines and their use in the treatment of cancer
AR056347A1 (en) 2005-05-12 2007-10-03 Tibotec Pharm Ltd USE OF PTERIDINE COMPOUNDS TO MANUFACTURE PHARMACEUTICAL MEDICINES AND COMPOSITIONS
US20080287437A1 (en) 2005-05-16 2008-11-20 Astrazeneca Ab Pyrazolylaminopyrimidine Derivatives Useful as Tyrosine Kinase Inhibitors
CA2612788A1 (en) 2005-06-24 2006-12-28 Steven Cesar Alfons De Jonghe Pyrido(3,2-d)pyrimidines and pharmaceutical compositions useful for treating hepatitis c
ES2270715B1 (en) 2005-07-29 2008-04-01 Laboratorios Almirall S.A. NEW DERIVATIVES OF PIRAZINA.
EP1917259B1 (en) * 2005-08-18 2012-01-25 Vertex Pharmaceuticals Incorporated Pyrazine kinase inhibitors
WO2007023382A2 (en) * 2005-08-25 2007-03-01 Pfizer Inc. Pyrimidine amino pyrazole compounds, potent kinase inhibitors
CA2620333A1 (en) 2005-08-26 2007-03-01 Braincells, Inc. Neurogenesis by muscarinic receptor modulation
EP2258358A3 (en) 2005-08-26 2011-09-07 Braincells, Inc. Neurogenesis with acetylcholinesterase inhibitor
US7915286B2 (en) 2005-09-16 2011-03-29 Ranbaxy Laboratories Limited Substituted pyrazolo [3,4-b] pyridines as phosphodiesterase inhibitors
CN101316587B (en) * 2005-09-30 2013-04-03 迈卡纳治疗股份有限公司 Substituted pyrazole compounds
EP1928456B1 (en) * 2005-09-30 2015-04-22 Miikana Therapeutics, Inc. Substituted pyrazole compounds
ES2274712B1 (en) 2005-10-06 2008-03-01 Laboratorios Almirall S.A. NEW IMIDAZOPIRIDINE DERIVATIVES.
US8119655B2 (en) 2005-10-07 2012-02-21 Takeda Pharmaceutical Company Limited Kinase inhibitors
GB0520657D0 (en) * 2005-10-11 2005-11-16 Ludwig Inst Cancer Res Pharmaceutical compounds
EP1940389A2 (en) 2005-10-21 2008-07-09 Braincells, Inc. Modulation of neurogenesis by pde inhibition
US20080287475A1 (en) * 2005-10-28 2008-11-20 Astrazeneca Ab 4-(3-Aminopyrazole) Pyrimidine Derivatives for Use as Tyrosine Kinase Inhibitors in the Treatment of Cancer
JP2009513672A (en) 2005-10-31 2009-04-02 ブレインセルス，インコーポレイティド GABA receptor-mediated regulation of neurogenesis
BRPI0619704A2 (en) * 2005-11-03 2011-10-11 Vertex Pharma compound, composition, method for inhibiting aurora kinase activity in a biological sample, method for treating a proliferative disorder and method for treating cancer
DK2404919T3 (en) 2005-11-08 2013-11-04 Vertex Pharma Heterocyclic compound suitable as modulator of ATP binding cassette transporters
US7713987B2 (en) 2005-12-06 2010-05-11 Rigel Pharmaceuticals, Inc. Pyrimidine-2,4-diamines and their uses
US8546404B2 (en) 2005-12-13 2013-10-01 Merck Sharp & Dohme Compounds that are ERK inhibitors
US7572809B2 (en) 2005-12-19 2009-08-11 Hoffmann-La Roche Inc. Isoquinoline aminopyrazole derivatives
US20070244169A1 (en) * 2005-12-20 2007-10-18 Jun Feng Glucokinase activators
EP2559694A3 (en) 2006-01-17 2013-04-03 Vertex Pharmaceuticals, Inc. Azaindoles useful as inhibitors of Janus kinases
JO2660B1 (en) 2006-01-20 2012-06-17 نوفارتيس ايه جي PI-3 Kinase inhibitors and methods of their use
KR20080103996A (en) 2006-02-16 2008-11-28 쉐링 코포레이션 Pyrrolidine derivatives as erk inhibitors
US20100216734A1 (en) 2006-03-08 2010-08-26 Braincells, Inc. Modulation of neurogenesis by nootropic agents
US20070244143A1 (en) * 2006-03-08 2007-10-18 Braincells, Inc Modulation of neurogenesis by nootropic agents
PE20080145A1 (en) 2006-03-21 2008-02-11 Janssen Pharmaceutica Nv TETRAHYDRO-PYRIMIDOAZEPINE AS MODULATORS OF TRPV1
JP2009536617A (en) * 2006-04-11 2009-10-15 バーテックス ファーマシューティカルズ インコーポレイテッド Thiazoles, imidazoles, and pyrazoles useful as inhibitors of protein kinases
US8158627B2 (en) 2006-04-28 2012-04-17 Northwestern University Compositions and treatments using pyridazine compounds and cholinesterase inhibitors
CA2651862A1 (en) 2006-05-09 2007-11-22 Braincells, Inc. 5 ht receptor mediated neurogenesis
US20100009983A1 (en) * 2006-05-09 2010-01-14 Braincells, Inc. 5 ht receptor mediated neurogenesis
JP2009536669A (en) 2006-05-09 2009-10-15 ブレインセルス，インコーポレイティド Neurogenesis by angiotensin regulation
TWI354668B (en) * 2006-06-27 2011-12-21 Takeda Pharmaceutical Fused cyclic compounds
CA2654852A1 (en) * 2006-06-30 2008-01-03 Astrazeneca Ab Pyrimidine derivatives useful in the treatment of cancer
WO2008005538A2 (en) * 2006-07-05 2008-01-10 Exelixis, Inc. Methods of using igf1r and abl kinase modulators
UA95641C2 (en) * 2006-07-06 2011-08-25 Эррей Биофарма Инк. Hydroxylated cyclopenta [d] pyrimidines as akt protein kinase inhibitors
US8063050B2 (en) 2006-07-06 2011-11-22 Array Biopharma Inc. Hydroxylated and methoxylated pyrimidyl cyclopentanes as AKT protein kinase inhibitors
AU2007269052B2 (en) * 2006-07-06 2014-10-23 Array Biopharma Inc. Cyclopenta [D] pyrimidines as AKT protein kinase inhibitors
US8338435B2 (en) 2006-07-20 2012-12-25 Gilead Sciences, Inc. Substituted pyrido(3,2-D) pyrimidines and pharmaceutical compositions for treating viral infections
WO2008030651A1 (en) * 2006-09-08 2008-03-13 Braincells, Inc. Combinations containing a 4-acylaminopyridine derivative
US20100184806A1 (en) 2006-09-19 2010-07-22 Braincells, Inc. Modulation of neurogenesis by ppar agents
CA2663347A1 (en) * 2006-09-19 2008-03-27 Braincells, Inc. Ppar mediated modulation of neurogenesis
EP2223925A1 (en) * 2006-10-09 2010-09-01 Takeda Pharmaceutical Company Limited Kinase inhibitors
SG158147A1 (en) 2006-10-09 2010-01-29 Takeda Pharmaceutical Kinase inhibitors
JP5406030B2 (en) * 2006-10-21 2014-02-05 アボット ゲーエムベーハー ウント カンパニー カーゲー Heterocyclic compounds and their use as glycogen synthase kinase 3 inhibitors
JP2010509231A (en) * 2006-11-02 2010-03-25 バーテックス ファーマシューティカルズ インコーポレイテッド Aminopyridines and aminopyrimidines useful as inhibitors of protein kinases
CA2673353A1 (en) * 2006-12-19 2008-06-26 Vertex Pharmaceuticals Incorporated Aminopyrimidines useful as inhibitors of protein kinases
WO2008077649A1 (en) 2006-12-26 2008-07-03 Gilead Sciences, Inc. Pyrido(3,2-d)pyrimidines useful for treating viral infectons
TW200840584A (en) 2006-12-26 2008-10-16 Gilead Sciences Inc Pyrido(3,2-d)pyrimidines useful for treating viral infections
US8637531B2 (en) 2006-12-26 2014-01-28 Gilead Sciences, Inc. Pyrido(3,2-d)pyridmidines useful for treating viral infections
WO2008098058A1 (en) 2007-02-06 2008-08-14 Novartis Ag Pi 3-kinase inhibitors and methods of their use
AU2008215948A1 (en) * 2007-02-12 2008-08-21 Merck & Co., Inc. Piperazine derivatives for treatment of AD and related conditions
JP2010518083A (en) * 2007-02-12 2010-05-27 メルク・シャープ・エンド・ドーム・コーポレイション Piperidine derivatives
CA2680122A1 (en) 2007-03-05 2008-09-18 Kyowa Hakko Kirin Co., Ltd. Pharmaceutical composition
WO2008112651A2 (en) * 2007-03-09 2008-09-18 Vertex Pharmaceuticals Incorporated Aminopyrimidines useful as inhibitors of protein kinases
EP2134709A1 (en) 2007-03-09 2009-12-23 Vertex Pharmaceuticals, Inc. Aminopyridines useful as inhibitors of protein kinases
CA2679884A1 (en) * 2007-03-09 2008-09-18 Vertex Pharmaceuticals Incorporated Aminopyrimidines useful as inhibitors of protein kinases
NZ580343A (en) 2007-04-13 2012-03-30 Vertex Pharma Aminopyrimidines useful as kinase inhibitors
US20100204246A1 (en) * 2007-04-18 2010-08-12 Astrazeneca Ab 5-aminopyrazol-3-yl-3h-imidazo (4,5-b) pyridine derivatives and their use for the treatment of cancer
MX2009011810A (en) 2007-05-02 2010-01-14 Vertex Pharma Thiazoles and pyrazoles useful as kinase inhibitors.
WO2008137621A1 (en) * 2007-05-02 2008-11-13 Vertex Pharmaceuticals Incorporated Aminopyrimidines useful as kinase inhibitors
MX2009011811A (en) * 2007-05-02 2010-01-14 Vertex Pharma Aminopyrimidines useful as kinase inhibitors.
UA99459C2 (en) * 2007-05-04 2012-08-27 Астразенека Аб 9-(pyrazol-3-yl)- 9h-purine-2-amine and 3-(pyraz0l-3-yl)-3h-imidazo[4,5-b]pyridin-5-amine derivatives and their use for the treatment of cancer
WO2008135786A1 (en) * 2007-05-04 2008-11-13 Astrazeneca Ab Amino-thiazolyl- pyrimidine derivatives and their use for the treatment of cancer
AU2008251504B2 (en) 2007-05-09 2013-07-18 Vertex Pharmaceuticals Incorporated Modulators of CFTR
JP2010528021A (en) * 2007-05-24 2010-08-19 バーテックス ファーマシューティカルズ インコーポレイテッド Thiazoles and pyrazoles useful as kinase inhibitors
WO2008154026A1 (en) * 2007-06-11 2008-12-18 Miikana Therapeutics, Inc. Substituted pyrazole compounds
US8242150B2 (en) * 2007-06-13 2012-08-14 Merck Sharp & Dohme Corp. Triazole derivatives for treating alzheimer'S disease and related conditions
WO2009000489A1 (en) 2007-06-25 2008-12-31 F. Hoffmann-La Roche Ag Benzimidazole amido derivatives as kinase inhibitors
US9409886B2 (en) 2007-07-05 2016-08-09 Array Biopharma Inc. Pyrimidyl cyclopentanes as AKT protein kinase inhibitors
MX2009014013A (en) * 2007-07-05 2010-01-28 Array Biopharma Inc Pyrimidyl cyclopentanes as akt protein kinase inhibitors.
US8846683B2 (en) 2007-07-05 2014-09-30 Array Biopharma, Inc. Pyrimidyl cyclopentanes as Akt protein kinase inhibitors
RU2486181C2 (en) 2007-07-05 2013-06-27 Эррэй Биофарма Инк. Pyrimidyl cyclopentanes as akt/protein kinase inhibitors
WO2009015254A1 (en) 2007-07-25 2009-01-29 Bristol-Myers Squibb Company Triazine kinase inhibitors
TW200906818A (en) * 2007-07-31 2009-02-16 Astrazeneca Ab Chemical compounds
TW200916468A (en) * 2007-07-31 2009-04-16 Vertex Pharma Process for preparing 5-fluoro-1H-pyrazolo[3,4-b]pyridin-3-amine and derivatives thereof
RU2010125220A (en) * 2007-11-20 2011-12-27 Мерк Шарп Энд Домэ Корп. (Us) NON-NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS
BRPI0821039B8 (en) 2007-12-07 2021-05-25 Vertex Pharma solid forms of 3-(6-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)-3-methylpyridin-2-yl)benzoic acid, process for their preparation , pharmaceutical compositions comprising the same and uses
MX2010006183A (en) 2007-12-07 2010-10-15 Vertex Pharma Processes for producing cycloalkylcarboxiamido-pyridine benzoic acids.
JP2011032169A (en) * 2007-12-11 2011-02-17 Genecare Research Institute Co Ltd 4-aminopyrimidine derivative and medicinal composition containing the compound
TW200942549A (en) 2007-12-17 2009-10-16 Janssen Pharmaceutica Nv Imidazolo-, oxazolo-, and thiazolopyrimidine modulators of TRPV1
TW200940542A (en) 2008-01-09 2009-10-01 Array Biopharma Inc Pyrimidyl cyclopentanes as AKT protein kinase inhibitors
WO2009089462A1 (en) * 2008-01-09 2009-07-16 Array Biopharma Inc. 5h-cyclopenta[d]pyrimidines as akt protein kinase inhibitors
RU2525389C2 (en) 2008-02-21 2014-08-10 Мерк Шарп И Доум Корп. Compounds which are erk inhibitors
JP5523352B2 (en) 2008-02-28 2014-06-18 バーテックス ファーマシューティカルズ インコーポレイテッド Heteroaryl derivatives as CFTR modifiers
EP2262498A2 (en) * 2008-03-10 2010-12-22 Vertex Pharmceuticals Incorporated Pyrimidines and pyridines useful as inhibitors of protein kinases
CL2009000904A1 (en) 2008-04-21 2010-04-30 Shionogi & Co Compounds derived from cyclohexyl sulfonamides having antagonist activity at the npy y5 receptor, pharmaceutical composition and pharmaceutical formulation comprising them.
US8158656B2 (en) * 2008-05-16 2012-04-17 Shenzhen Chipscreen Biosciences Ltd. 2-indolinone derivatives as multi-target protein kinase inhibitors and histone deacetylase inhibitors
SI2300013T1 (en) 2008-05-21 2018-03-30 Adriad Pharmacaceuticals, Inc. Phosphorous derivatives as kinase inhibitors
CN102119157A (en) * 2008-06-11 2011-07-06 阿斯利康(瑞典)有限公司 Tricyclic 2,4-diamino-L,3,5-triazine derivatives useful for the treatment of cancer and myeloproliferative disorders
JP5658662B2 (en) 2008-06-12 2015-01-28 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプＪａｎｓｓｅｎ Ｐｈａｒｍａｃｅｕｔｉｃａ Ｎａａｍｌｏｚｅ Ｖｅｎｎｏｏｔｓｃｈａｐ Diaminopyridine, pyrimidine, and pyridazine modulators of histamine H4 receptor
WO2010002998A1 (en) 2008-07-03 2010-01-07 Gilead Sciences, Inc. 2,4,6-TRISUBSTITUTED PYRIDO (3,2-d) PYRIMIDINES USEFUL FOR TREATING VIRAL INFECTIONS
EP2291376A2 (en) * 2008-07-03 2011-03-09 Merck Patent GmbH Naphthyridininones as aurora kinase inhibitors
JP2011529920A (en) 2008-07-31 2011-12-15 ジェネンテック， インコーポレイテッド Pyrimidine compounds, compositions and methods of use
US20110251172A1 (en) * 2008-08-13 2011-10-13 Rivkin Alexey A Purine derivatives for treatment of alzheimer's disease
MX2011002312A (en) * 2008-09-03 2011-04-26 Vertex Pharma Co-crystals and pharmaceutical formulations comprising the same.
AU2009290617B2 (en) * 2008-09-15 2015-05-14 Fundacion Ciencia Para La Vida Methods and compositions for modulating Ire1, Src, and Abl activity
EP2346859A1 (en) * 2008-09-30 2011-07-27 AstraZeneca AB Heterocyclic jak kinase inhibitors
CA2744343A1 (en) * 2008-11-19 2010-05-27 Renovis, Inc. 6, 7 -dihydro- 5h- pyrrolo [3, 4-d] pyrimidin-4-yl] -quinolin-3 -ylamine compounds useful as faah modulators and uses thereof
KR101048448B1 (en) 2008-11-21 2011-07-11 한국화학연구원 Novel pyrazolo [4,3-ｂ] pyridine derivatives or pharmaceutically acceptable salts thereof, preparation methods thereof and pharmaceutical compositions containing the same as active ingredients
AR075238A1 (en) 2009-02-05 2011-03-16 Takeda Pharmaceutical PIRIDAZINONA COMPOUNDS
WO2010099217A1 (en) 2009-02-25 2010-09-02 Braincells, Inc. Modulation of neurogenesis using d-cycloserine combinations
JP5746981B2 (en) * 2009-02-27 2015-07-08 アムビト ビオスシエンセス コルポラチオン JAK kinase-regulated quinazoline derivatives and methods of use thereof
CA2755095A1 (en) * 2009-03-09 2010-09-16 Surface Logix, Inc. Rho kinase inhibitors
WO2010111050A1 (en) 2009-03-23 2010-09-30 Banyu Pharmaceutical Co., Ltd. Novel aminopyridine derivatives having aurora a selective inhibitory action
EP2411012A4 (en) * 2009-03-24 2012-08-22 Msd Kk Novel aminopyridine derivatives having aurora a selective inhibitory action
KR20120004467A (en) * 2009-03-24 2012-01-12 엠에스디 가부시키가이샤 Novel aminopyridine derivatives having aurora a selective inhibitory action
US8211901B2 (en) 2009-05-22 2012-07-03 Shenzhen Chipscreen Biosciences Ltd. Naphthamide derivatives as multi-target protein kinase inhibitors and histone deacetylase inhibitors
CN101906076B (en) 2009-06-04 2013-03-13 深圳微芯生物科技有限责任公司 Naphthaline amide derivative serving as protein kinase inhibitor and histone deacetylase inhibitor and preparation method and application thereof
WO2010144338A1 (en) * 2009-06-08 2010-12-16 Abraxis Bioscience, Llc Triazine derivatives and their therapeutical applications
JP5785940B2 (en) * 2009-06-09 2015-09-30 アブラクシス バイオサイエンス， エルエルシー Triazine derivatives and their therapeutic applications
KR20120016676A (en) * 2009-06-09 2012-02-24 아브락시스 바이오사이언스, 엘엘씨 Ureidophenyl substituted triazine derivatives and their therapeutical applications
WO2010151601A1 (en) * 2009-06-24 2010-12-29 Genentech, Inc. Oxo-heterocycle fused pyrimidine compounds, compositions and methods of use
US8637525B2 (en) 2009-07-31 2014-01-28 Bristol-Myers Squibb Company Compounds for the reduction of beta-amyloid production
TWI468402B (en) * 2009-07-31 2015-01-11 必治妥美雅史谷比公司 Compounds for the reduction of β-amyloid production
US20110053916A1 (en) * 2009-08-14 2011-03-03 Vertex Pharmaceuticals Incorporated Pyrimidine compounds as tuberculosis inhibitors
CN102020657A (en) * 2009-09-11 2011-04-20 上海艾力斯医药科技有限公司 Condensed heteroaryl derivative, and preparation method and application thereof
RU2607635C2 (en) 2009-11-12 2017-01-10 Ф.Хоффманн-Ля Рош Аг N-9-substituted purine compounds, compositions and methods of use
RU2515541C2 (en) 2009-11-12 2014-05-10 Ф.Хоффманн-Ля Рош Аг N-7 substituted purines and pyrazolopyrimidines, compositions thereof and methods for use
KR20130029368A (en) * 2010-02-11 2013-03-22 벤더르빌트 유니버시티 Pyrazolopyridine, pyrazolopyrazine, pyrazolopyrimidine, pyrazolothiophene and pyrazolothiazole compounds as mglur4 allosteric potentiators, compounds, and methods of treating neurological dysfunction
JP2013523833A (en) 2010-04-07 2013-06-17 バーテックス ファーマシューティカルズ インコーポレイテッド 3- (6- (1- (2,2-difluorobenzo [D] [1,3] dioxol-5-yl) cyclopropanecarboxamido) -3-methylpyridin-2-yl) benzoic acid pharmaceutical composition and Its administration
EP2571867B1 (en) 2010-05-21 2015-11-04 Noviga Research AB Novel pyrimidine derivatives
US8354420B2 (en) 2010-06-04 2013-01-15 Genentech, Inc. Aminopyrimidine derivatives as LRRK2 inhibitors
US20110319409A1 (en) * 2010-06-23 2011-12-29 Cox Christopher D 7-aza-quinazoline pde10 inhibitors
EP2611789A1 (en) 2010-09-01 2013-07-10 Ambit Biosciences Corporation Quinazoline compounds and methods of use thereof
EP2621914B1 (en) 2010-09-27 2016-12-28 Abbott GmbH & Co. KG Heterocyclic compounds and their use as glycogen synthase kinase-3 inhibitors
WO2012059932A1 (en) 2010-11-01 2012-05-10 Aurigene Discovery Technologies Limited 2, 4 -diaminopyrimidine derivatives as protein kinase inhibitors
CA2816957A1 (en) 2010-11-07 2012-05-10 Targegen, Inc. Compositions and methods for treating myelofibrosis
PT3124483T (en) 2010-11-10 2019-10-02 Genentech Inc Pyrazole aminopyrimidine derivatives as lrrk2 modulators
US20140018540A1 (en) 2010-12-14 2014-01-16 Electrophoretics Limited Casein kinase 1delta (ck 1delta) inhibitors
BR112013015449A2 (en) 2010-12-21 2016-09-20 Novartis Ag biheteroaryl compounds as vps23 inhibitors
US9090592B2 (en) 2010-12-30 2015-07-28 AbbVie Deutschland GmbH & Co. KG Heterocyclic compounds and their use as glycogen synthase kinase-3 inhibitors
US9481670B2 (en) * 2011-01-25 2016-11-01 Sphaera Pharma Pte. Ltd. Triazine compounds
KR20140006048A (en) 2011-03-24 2014-01-15 케밀리아 에이비 Novel pyrimidine derivatives
KR20140021646A (en) 2011-04-01 2014-02-20 제넨테크, 인크. Combinations of akt inhibitor compounds and erlotinib, and methods of use
EP2694073B1 (en) 2011-04-01 2018-08-08 Genentech, Inc. Combinations of akt and mek inhibitors for treating cancer
RU2477723C2 (en) 2011-06-16 2013-03-20 Общество С Ограниченной Ответственностью "Фьюжн Фарма" Protein kinase inhibitor (versions), use thereof for treating oncological diseases and based pharmaceutical composition
AU2012284088B2 (en) 2011-07-19 2015-10-08 Infinity Pharmaceuticals Inc. Heterocyclic compounds and uses thereof
US8846656B2 (en) 2011-07-22 2014-09-30 Novartis Ag Tetrahydropyrido-pyridine and tetrahydropyrido-pyrimidine compounds and use thereof as C5a receptor modulators
CA2844729A1 (en) 2011-08-25 2013-02-28 F. Hoffmann-La Roche Ag Serine/threonine pak1 inhibitors
RU2627693C2 (en) 2011-09-14 2017-08-10 СЭМЬЮМЕД, ЭлЭлСи INDAZOLE-3-CARBOXAMIDES AND THEIR USE AS WNT/β-CATENIN SIGNAL INHIBITORS
MD20140023A2 (en) 2011-09-22 2014-06-30 Pfizer Inc. Pyrrolopyrimidine and purine derivatives
BR112014007310A2 (en) 2011-09-27 2017-04-04 Novartis Ag 3-pyrimidin-4-yl-oxazolidin-2-ones as mutant idh inhibitors
WO2013092940A1 (en) 2011-12-22 2013-06-27 F. Hoffmann-La Roche Ag 2, 4-diamine-pyrimidine derivative as serine/threonine kinase inhibitors
UY34632A (en) 2012-02-24 2013-05-31 Novartis Ag OXAZOLIDIN- 2- ONA COMPOUNDS AND USES OF THE SAME
WO2013138617A1 (en) * 2012-03-16 2013-09-19 Axikin Pharmaceuticals, Inc. 3,5-diaminopyrazole kinase inhibitors
WO2013140148A1 (en) * 2012-03-19 2013-09-26 Imperial Innovations Limited Quinazoline compounds and their use in therapy
US20130303519A1 (en) 2012-03-20 2013-11-14 Millennium Pharmaceuticals, Inc. Methods of treating cancer using aurora kinase inhibitors
PH12017500997A1 (en) 2012-04-04 2018-02-19 Samumed Llc Indazole inhibitors of the wnt signal pathway and therapeutic uses thereof
SI2841428T1 (en) 2012-04-24 2018-12-31 Vertex Pharmaceuticals Incorporated Dna-pk inhibitors
MX358172B (en) * 2012-05-03 2018-08-08 Genentech Inc Pyrazole aminopyrimidine derivatives as lrrk2 modulators for use in the treatment of parkinson's disease.
CA2870049C (en) * 2012-05-03 2020-12-29 Charles Baker-Glenn Pyrazole aminopyrimidine derivatives as lrrk2 modulators
SG10201805807PA (en) 2012-06-26 2018-08-30 Del Mar Pharmaceuticals Methods for treating tyrosine-kinase-inhibitor-resistant malignancies in patients with genetic polymorphisms or ahi1 dysregulations or mutations employing dianhydrogalactitol, diacetyldianhydrogalactitol, dibromodulcitol, or analogs or derivatives thereof
TWI663165B (en) 2012-09-28 2019-06-21 美商伊格尼塔公司 Azaquinazoline inhibitors of atypical protein kinase c
JO3470B1 (en) 2012-10-08 2020-07-05 Merck Sharp & Dohme 5-phenoxy-3h-pyrimidin-4-one derivatives and their use as hiv reverse transcriptase inhibitors
WO2014062838A2 (en) 2012-10-16 2014-04-24 Tolero Pharmaceuticals, Inc. Pkm2 modulators and methods for their use
US9296733B2 (en) 2012-11-12 2016-03-29 Novartis Ag Oxazolidin-2-one-pyrimidine derivative and use thereof for the treatment of conditions, diseases and disorders dependent upon PI3 kinases
KR20150087850A (en) * 2012-11-20 2015-07-30 제넨테크, 인크. Aminopyrimidine compounds as inhibitors of t790m containing egfr mutants
WO2014081906A2 (en) 2012-11-21 2014-05-30 Ptc Therapeutics, Inc. Substituted reverse pyrimidine bmi-1 inhibitors
CN103012428A (en) 2013-01-08 2013-04-03 中国药科大学 4-(five-membered heterocycle pyrimidin/substituted pyridine) amino-1H-3-pyrazolecarboxamide CDK (cyclin dependent kinase)/Aurora dual inhibitor and application thereof
EP2943198B1 (en) 2013-01-08 2019-07-17 Samumed, LLC 3-(benzoimidazol-2-yl)-indazole inhibitors of the wnt signaling pathway and therapeutic uses thereof
US9745328B2 (en) 2013-02-04 2017-08-29 Janssen Pharmaceutica Nv Flap modulators
TWI644899B (en) 2013-02-04 2018-12-21 健生藥品公司 Flap modulators
EP2769722A1 (en) * 2013-02-22 2014-08-27 Ruprecht-Karls-Universität Heidelberg Compounds for use in inhibiting HIV capsid assembly
JO3377B1 (en) * 2013-03-11 2019-03-13 Takeda Pharmaceuticals Co Pyridinyl and fused pyridinyl triazolone derivatives
CN107200749B (en) 2013-03-12 2019-09-03 沃泰克斯药物股份有限公司 DNA-PK inhibitor
EP2970240B1 (en) 2013-03-14 2018-01-10 Novartis AG 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh
WO2014153509A1 (en) 2013-03-22 2014-09-25 Millennium Pharmaceuticals, Inc. Combination of catalytic mtorc 1/2 inhibitors and selective inhibitors of aurora a kinase
EP3024457A4 (en) 2013-07-26 2017-06-28 Update Pharma Inc. Compositions to improve the therapeutic benefit of bisantrene
EP3039015B1 (en) 2013-08-30 2019-10-30 PTC Therapeutics, Inc. Substituted pyrimidine bmi-1 inhibitors
WO2015028848A1 (en) * 2013-09-02 2015-03-05 Piramal Enterprises Limited Bicyclic heterocyclic compounds as multi-kinase inhibitors
CN105636586B (en) 2013-10-03 2018-05-29 库拉肿瘤学公司 ERK inhibitor and application method
WO2015054317A1 (en) 2013-10-07 2015-04-16 Kadmon Corporation, Llc Rho kinase inhibitors
EP3057953B1 (en) 2013-10-17 2018-08-15 Vertex Pharmaceuticals Incorporated Co-crystals of (s)-n-methyl-8-(1-((2'-methyl-[4,5'-bipyrimidin]-6-yl)amino)propan-2-yl)quinoline-4-carboxamide and deuterated derivatives thereof as dna-pk inhibitors
CN105848657B (en) 2013-11-12 2020-05-22 沃泰克斯药物股份有限公司 Methods of making pharmaceutical compositions for treating CFTR mediated diseases
US10584115B2 (en) 2013-11-21 2020-03-10 Ptc Therapeutics, Inc. Substituted pyridine and pyrazine BMI-1 inhibitors
WO2015076801A1 (en) * 2013-11-21 2015-05-28 Ptc Therapeutics, Inc. Substituted triazine bmi-1 inhibitors
UA115388C2 (en) 2013-11-21 2017-10-25 Пфайзер Інк. 2,6-substituted purine derivatives and their use in the treatment of proliferative disorders
CN104672250B (en) * 2013-11-29 2017-11-07 广东东阳光药业有限公司 Substituted heteroaryl compound and combinations thereof and purposes
CN109045032A (en) 2014-01-01 2018-12-21 麦迪威森技术有限责任公司 Aminopyridines and application method
WO2015112739A1 (en) * 2014-01-22 2015-07-30 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Compounds and method for treating parp1-deficient cancers
CN104926794B (en) * 2014-03-17 2017-12-05 广东东阳光药业有限公司 Substituted heteroaryl compound and combinations thereof and purposes
TWI675836B (en) * 2014-03-25 2019-11-01 美商伊格尼塔公司 Azaquinazoline inhibitors of atypical protein kinase c
US20170165230A1 (en) 2014-04-09 2017-06-15 Christopher Rudd Use of gsk-3 inhibitors or activators which modulate pd-1 or t-bet expression to modulate t cell immunity
CN105367555B (en) * 2014-08-07 2019-06-25 广东东阳光药业有限公司 Substituted heteroaryl compound and combinations thereof and purposes
WO2016040181A1 (en) 2014-09-08 2016-03-17 Samumed, Llc 3-(1h-imidazo[4,5-c]pyridin-2-yl)-1h-pyrazolo[3,4-c]pyridine and therapeutic uses thereof
WO2016040190A1 (en) 2014-09-08 2016-03-17 Samumed, Llc 3-(3h-imidazo[4,5-b]pyridin-2-yl)-1h-pyrazolo[3,4-b]pyridine and therapeutic uses thereof
WO2016040185A1 (en) 2014-09-08 2016-03-17 Samumed, Llc 2-(1h-indazol-3-yl)-3h-imidazo[4,5-b]pyridine and therapeutic uses thereof
WO2016040184A1 (en) 2014-09-08 2016-03-17 Samumed, Llc 3-(3h-imidazo[4,5-b]pyridin-2-yl)-1h-pyrazolo[3,4-c]pyridine and therapeutic uses thereof
WO2016040193A1 (en) 2014-09-08 2016-03-17 Samumed, Llc 3-(1h-imidazo[4,5-c]pyridin-2-yl)-1h-pyrazolo[3,4-b]pyridine and therapeutic uses thereof
WO2016040180A1 (en) 2014-09-08 2016-03-17 Samumed, Llc 3-(1h-benzo[d]imidazol-2-yl)-1h-pyrazolo[3,4-c]pyridine and therapeutic uses thereof
HUE055423T2 (en) 2014-11-18 2021-11-29 Vertex Pharma Process of conducting high throughput testing high performance liquid chromatography
ES2700200T3 (en) * 2014-12-22 2019-02-14 Lilly Co Eli ERK inhibitors
TWI704151B (en) * 2014-12-22 2020-09-11 美商美國禮來大藥廠 Erk inhibitors
US10227343B2 (en) 2015-01-30 2019-03-12 Vanderbilt University Isoquiniline and napthalene-substituted compounds as mGluR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction
EP3070084A1 (en) * 2015-03-18 2016-09-21 Rottapharm Biotech S.r.l. New fyn kinase inhibitors
WO2016166604A1 (en) 2015-04-17 2016-10-20 Ludwig Institute For Cancer Research Ltd Plk4 inhibitors
US10118904B2 (en) 2015-06-05 2018-11-06 Vertex Pharmaceuticals Incorporated Triazoles for the treatment of Demyelinating Diseases
US10285982B2 (en) 2015-08-03 2019-05-14 Samumed, Llc 3-(1H-pyrrolo[2,3-B]pyridin-2-yl)-1H-pyrazolo[3,4-C]pyridines and therapeutic uses thereof
WO2017023987A1 (en) 2015-08-03 2017-02-09 Samumed, Llc. 3-(1h-pyrrolo[3,2-c]pyridin-2-yl)-1h-pyrazolo[3,4-b]pyridines and therapeutic uses thereof
US10519169B2 (en) 2015-08-03 2019-12-31 Samumed, Llc 3-(1H-pyrrolo[2,3-C]pyridin-2-yl)-1 H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
US10206908B2 (en) 2015-08-03 2019-02-19 Samumed, Llc 3-(1H-pyrrolo[3,2-C]pyridin-2-YL)-1H-pyrazolo[3,4-C]pyridines and therapeutic uses thereof
US10206909B2 (en) 2015-08-03 2019-02-19 Samumed, Llc 3-(1H-pyrrolo[2,3-B]pyridin-2-yl)-1H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
WO2017023993A1 (en) 2015-08-03 2017-02-09 Samumed, Llc. 3-(1h-indol-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof
WO2017023972A1 (en) 2015-08-03 2017-02-09 Samumed, Llc. 3-(1h-imidazo[4,5-c]pyridin-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof
WO2017024026A1 (en) 2015-08-03 2017-02-09 Samumed, Llc 3-(1h-indol-2-yl)-1h-pyrazolo[3,4-c]pyridines and therapeutic uses thereof
US10383861B2 (en) 2015-08-03 2019-08-20 Sammumed, LLC 3-(1H-pyrrolo[2,3-C]pyridin-2-yl)-1H-pyrazolo[3,4-C]pyridines and therapeutic uses thereof
US10285983B2 (en) 2015-08-03 2019-05-14 Samumed, Llc 3-(1H-pyrrolo[2,3-B]pyridin-2-yl)-1H-pyrazolo[3,4-B] pyridines and therapeutic uses thereof
US10231956B2 (en) 2015-08-03 2019-03-19 Samumed, Llc 3-(1H-pyrrolo[3,2-C]pyridin-2-YL)-1 H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
US10350199B2 (en) 2015-08-03 2019-07-16 Samumed, Llc 3-(1h-pyrrolo[2,3-b]pyridin-2-yl)-1h-indazoles and therapeutic uses thereof
WO2017023989A1 (en) 2015-08-03 2017-02-09 Samumed, Llc. 3-(1h-benzo[d]imidazol-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof
US10188634B2 (en) 2015-08-03 2019-01-29 Samumed, Llc 3-(3H-imidazo[4,5-C]pyridin-2-yl)-1 H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
WO2017024015A1 (en) * 2015-08-03 2017-02-09 Samumed, Llc. 3-(3h-imidazo[4,5-b]pyridin-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof
WO2017023986A1 (en) 2015-08-03 2017-02-09 Samumed, Llc 3-(1h-indol-2-yl)-1h-indazoles and therapeutic uses thereof
US10463651B2 (en) 2015-08-03 2019-11-05 Samumed, Llc 3-(1H-pyrrolo[3,2-C]pyridin-2-YL)-1H-indazoles and therapeutic uses thereof
CN108473491A (en) 2015-11-06 2018-08-31 萨穆梅德有限公司 2- (1H- indazole -3- bases) -3H- imidazos [4,5-C] pyridines and its antiphlogistic use
GB201604647D0 (en) * 2016-03-18 2016-05-04 Mission Therapeutics Ltd Novel compounds
TW201815418A (en) 2016-09-27 2018-05-01 Vertex Pharma Method for treating cancer using a combination of DNA-damaging agents and DNA-PK inhibitors
EP3528808B1 (en) 2016-10-21 2021-10-06 BioSplice Therapeutics, Inc. Methods of using indazole-3-carboxamides and their use as wnt/b-catenin signaling pathway inhibitors
CA3041332A1 (en) 2016-11-01 2018-05-11 Merck Sharp & Dohme Corp. Substituted bicyclic heteroaryl allosteric modulators of nicotinic acetylcholine receptors
KR102558716B1 (en) 2016-11-07 2023-07-21 사뮤메드, 엘엘씨 Single-dose, ready-to-use injectable formulation
IT201700047189A1 (en) * 2017-05-02 2018-11-02 Fondazione St Italiano Tecnologia COMPOUNDS AND COMPOSITIONS FOR CANCER TREATMENT, RETINAL DISORDERS AND CARDIOMYOPATHIES
AR112027A1 (en) * 2017-06-15 2019-09-11 Biocryst Pharm Inc ALK 2 KINASE INHIBITORS CONTAINING IMIDAZOLE
CN111217797B (en) 2017-06-30 2021-02-05 北京泰德制药股份有限公司 Rho-related protein kinase inhibitor, pharmaceutical composition containing same, and preparation method and application thereof
US10329282B2 (en) 2017-06-30 2019-06-25 Beijing Tide Pharmaceutical Co., Ltd. Rho-associated protein kinase inhibitor, pharmaceutical composition comprising the same, as well as preparation method and use thereof
US10323023B2 (en) 2017-06-30 2019-06-18 Beijing Tide Pharmaceutical Co., Ltd. Rho-associated protein kinase inhibitor, pharmaceutical composition comprising the same, as well as preparation method and use thereof
CN109384774B (en) * 2017-08-11 2023-02-17 中国科学院上海药物研究所 Polysubstituted pyrazine/triazine amide compounds and preparation method and application thereof
EA202091016A1 (en) 2017-10-27 2020-07-17 ТЕРЕВАНС БАЙОФАРМА Ар энд Ди АйПи, ЭлЭлСи PYRIMIDINE COMPOUND AS A JAK KINASE INHIBITOR
GB201801226D0 (en) 2018-01-25 2018-03-14 Redx Pharma Plc Modulators of Rho-associated protein kinase
WO2020005935A1 (en) * 2018-06-25 2020-01-02 Kadmon Corporation, Llc Glucose uptake inhibitors
KR102328682B1 (en) * 2018-08-27 2021-11-18 주식회사 대웅제약 Novel heterocyclicamine derivatives and pharmaceutical composition comprising the same
WO2020045941A1 (en) * 2018-08-27 2020-03-05 주식회사 대웅제약 Novel heterocyclic amine derivative and pharmaceutical composition comprising same
US11066404B2 (en) 2018-10-11 2021-07-20 Incyte Corporation Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors
AR117544A1 (en) 2018-12-27 2021-08-11 Agios Pharmaceuticals Inc HETEROCYCLIC INHIBITORS OF MAT2A AND METHODS OF USE FOR THE TREATMENT OF CANCER
US20220112218A1 (en) * 2019-01-03 2022-04-14 University Of Pittsburgh - Of The Commonwealth System Of Higher Education Methods and materials for increasing transcription factor eb polypeptide levels
WO2020163812A1 (en) 2019-02-08 2020-08-13 Frequency Therapeutics, Inc. Valproic acid compounds and wnt agonists for treating ear disorders
WO2020168197A1 (en) 2019-02-15 2020-08-20 Incyte Corporation Pyrrolo[2,3-d]pyrimidinone compounds as cdk2 inhibitors
WO2020180959A1 (en) 2019-03-05 2020-09-10 Incyte Corporation Pyrazolyl pyrimidinylamine compounds as cdk2 inhibitors
AU2020245437A1 (en) 2019-03-22 2021-09-30 Sumitomo Pharma Oncology, Inc. Compositions comprising PKM2 modulators and methods of treatment using the same
TW202102511A (en) 2019-03-28 2021-01-16 大陸商江蘇恆瑞醫藥股份有限公司 A thienyl fused heterocyclic derivative, a preparation method thereof, and medical applications thereof
KR20210146956A (en) 2019-03-29 2021-12-06 지앙수 헨그루이 메디슨 컴퍼니 리미티드 Pyrroloheterocyclic derivatives, methods for their preparation, and their applications in medicine
US11919904B2 (en) 2019-03-29 2024-03-05 Incyte Corporation Sulfonylamide compounds as CDK2 inhibitors
CN109826608A (en) * 2019-04-08 2019-05-31 中国科学院地质与地球物理研究所 A kind of segmented fracturing device
WO2020219640A1 (en) 2019-04-24 2020-10-29 Theravance Biopharma R&D Ip, Llc Pyrimidine jak inhibitors for the treatment of skin diseases
WO2020219639A1 (en) 2019-04-24 2020-10-29 Theravance Biopharma R&D Ip, Llc Ester and carbonate pyrimidine compounds as jak kinase inhibitors
WO2020223558A1 (en) 2019-05-01 2020-11-05 Incyte Corporation Tricyclic amine compounds as cdk2 inhibitors
US11440914B2 (en) 2019-05-01 2022-09-13 Incyte Corporation Tricyclic amine compounds as CDK2 inhibitors
EP3978498A1 (en) 2019-05-24 2022-04-06 Jiangsu Hengrui Medicine Co., Ltd. Substituted fused bicyclic derivative, preparation method therefor, and application thereof in medicines
EP3976584A1 (en) * 2019-05-29 2022-04-06 IFM Due, Inc. Compounds and compositions for treating conditions associated with sting activity
PE20221010A1 (en) 2019-08-14 2022-06-15 Incyte Corp IMIDAZOLIL PYRIMIDINILAMINE COMPOUNDS AS CDK2 INHIBITORS
WO2021043966A1 (en) * 2019-09-06 2021-03-11 Inflazome Limited Nlrp3 inhibitors
MX2022003617A (en) * 2019-10-02 2022-05-30 Tolremo Therapeutics Ag Heterocyclic derivatives, pharmaceutical compositions and their use in the treatment or amelioration of cancer.
JP2022551668A (en) 2019-10-11 2022-12-12 インサイト・コーポレイション Bicyclic amines as CDK2 inhibitors
AU2021226411A1 (en) * 2020-02-26 2022-09-22 Jaguahr Therapeutics Pte Ltd Pyridopyrimidine derivatives useful in modulation of AhR signalling
EP4182308A1 (en) 2020-07-15 2023-05-24 Chiesi Farmaceutici S.p.A. Pyridazinyl amino derivatives as alk5 inhibitors
WO2022032484A1 (en) * 2020-08-11 2022-02-17 北京诺诚健华医药科技有限公司 Pyridazine-3-formamide compound, and preparation method therefor and medical use thereof
WO2022068860A1 (en) 2020-09-29 2022-04-07 江苏恒瑞医药股份有限公司 Crystal form of pyrrolo heterocyclic derivative and preparation method therefor
WO2022107919A1 (en) * 2020-11-19 2022-05-27 주식회사 보로노이 N-containing heteroaryl derivative, and pharmaceutical composition for preventing or treating protein kinase-related diseases comprising same as active ingredient
US11932648B2 (en) 2021-06-28 2024-03-19 Blueprint Medicines Corporation CDK2 inhibitors
WO2023046698A1 (en) 2021-09-21 2023-03-30 Chiesi Farmaceutici S.P.A. Pyridazinyl amino derivatives as alk5 inhibitors
CN116023380B (en) * 2021-10-26 2024-01-23 沈阳药科大学 Pyrazolopyrimidine derivative, and preparation method and application thereof
WO2023135107A1 (en) 2022-01-11 2023-07-20 Chiesi Farmaceutici S.P.A. Pyridazinyl amino derivatives as alk5 inhibitors

Family Cites Families (120)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3133081A (en) * 1964-05-12 J-aminoindazole derivatives
US665330A (en) * 1899-12-18 1901-01-01 Antoine J Langelier Machine for making blanks for sewing-machine needles or similar articles.
US3935183A (en) * 1970-01-26 1976-01-27 Imperial Chemical Industries Limited Indazole-azo phenyl compounds
BE754242A (en) * 1970-07-15 1971-02-01 Geigy Ag J R DIAMINO-S-TRIAZINES AND DINITRO-S-TRIAZINES
US3998951A (en) 1974-03-13 1976-12-21 Fmc Corporation Substituted 2-arylquinazolines as fungicides
DE2458965C3 (en) 1974-12-13 1979-10-11 Bayer Ag, 5090 Leverkusen 3-Amino-indazole-N-carboxylic acid derivatives, process for their preparation and pharmaceuticals containing them
MA18829A1 (en) 1979-05-18 1980-12-31 Ciba Geigy Ag PYRIMIDINE DERIVATIVES, METHODS FOR THEIR PREPARATION, PHARMACEUTICAL COMPOSITIONS CONTAINING THESE COMPOUNDS AND THEIR THERAPEUTIC USE
DOP1981004033A (en) * 1980-12-23 1990-12-29 Ciba Geigy Ag PROCEDURE TO PROTECT CROP PLANTS FROM PHYTOTOXIC ACTION OF HERBICIDES.
SE8102193L (en) * 1981-04-06 1982-10-07 Pharmacia Ab THERAPEUTIC ACTIVE ORGANIC ASSOCIATION AND ITS USE
SE8102194L (en) * 1981-04-06 1982-10-07 Pharmacia Ab THERAPEUTIC ACTIVE ORGANIC ASSOCIATION AND PHARMACEUTICAL PREPARATION INCLUDING THIS
JPS58124773A (en) * 1982-01-20 1983-07-25 Mitsui Toatsu Chem Inc 5-methylthiopyrimidine derivative, its preparation and fungicide for agricultural and horticultural purposes
EP0136976A3 (en) 1983-08-23 1985-05-15 Ciba-Geigy Ag Use of phenyl pyrimidines as plant regulators
DE3725638A1 (en) 1987-08-03 1989-02-16 Bayer Ag NEW ARYLOXY (OR THIO) AMINOPYRIMIDINE
JPH0532662A (en) 1990-11-09 1993-02-09 Nissan Chem Ind Ltd Substituted pyrazole derivative and agricultural and horticultural fungicide
US5710158A (en) * 1991-05-10 1998-01-20 Rhone-Poulenc Rorer Pharmaceuticals Inc. Aryl and heteroaryl quinazoline compounds which inhibit EGF and/or PDGF receptor tyrosine kinase
US5597920A (en) * 1992-04-30 1997-01-28 Neurogen Corporation Gabaa receptor subtypes and methods for screening drug compounds using imidazoquinoxalines and pyrrolopyrimidines to bind to gabaa receptor subtypes
JP2657760B2 (en) 1992-07-15 1997-09-24 小野薬品工業株式会社 4-aminoquinazoline derivatives and pharmaceuticals containing them
ATE325113T1 (en) 1993-10-01 2006-06-15 Novartis Pharma Gmbh PHARMACOLOGICALLY ACTIVE PYRIMIDINE DERIVATIVES AND METHOD FOR THE PRODUCTION THEREOF
ES2219670T3 (en) 1994-11-10 2004-12-01 Millennium Pharmaceuticals, Inc. USE OF PIRAZOLA COMPOUNDS FOR THE TREATMENT OF GLOMERULONEFRITIS, CANCER, ATEROSCLEROSIS OR RESTENOSIS.
US5658902A (en) 1994-12-22 1997-08-19 Warner-Lambert Company Quinazolines as inhibitors of endothelin converting enzyme
IL117659A (en) 1995-04-13 2000-12-06 Dainippon Pharmaceutical Co Substituted 2-phenyl pyrimidino amino acetamide derivative process for preparing the same and a pharmaceutical composition containing same
WO1997009325A1 (en) 1995-09-01 1997-03-13 Signal Pharmaceuticals, Inc. Pyrimidine carboxylates and related compounds and methods for treating inflammatory conditions
GB9523675D0 (en) 1995-11-20 1996-01-24 Celltech Therapeutics Ltd Chemical compounds
AU7626496A (en) 1995-12-01 1997-06-27 Ciba-Geigy Ag Heteroaryl compounds
US6716575B2 (en) * 1995-12-18 2004-04-06 Sugen, Inc. Diagnosis and treatment of AUR1 and/or AUR2 related disorders
AU3766897A (en) * 1996-07-13 1998-02-09 Glaxo Group Limited Fused heterocyclic compounds as protein tyrosine kinase inhibitors
JPH10130150A (en) * 1996-09-05 1998-05-19 Dainippon Pharmaceut Co Ltd Medicine comprising acetic acid amide derivative
GB9619284D0 (en) 1996-09-16 1996-10-30 Celltech Therapeutics Ltd Chemical compounds
ATE291022T1 (en) 1996-10-02 2005-04-15 Novartis Pharma Gmbh PYRIMIDE DERIVATIVES AND PROCESS FOR THE PRODUCTION THEREOF
EP0932598A1 (en) 1996-10-11 1999-08-04 Warner-Lambert Company ASPARTATE ESTER INHIBITORS OF INTERLEUKIN-1$g(b) CONVERTING ENZYME
CA2306692C (en) 1997-10-10 2010-09-21 Cytovia, Inc. Dipeptide apoptosis inhibitors and the use thereof
DE19756388A1 (en) 1997-12-18 1999-06-24 Hoechst Marion Roussel De Gmbh New 2-aryl-4-amino-6,7-di:methoxy-quinazoline derivatives useful as guanylate cyclase activators for treating cardiovascular diseases, etc.
US6267952B1 (en) * 1998-01-09 2001-07-31 Geltex Pharmaceuticals, Inc. Lipase inhibiting polymers
JP2000026421A (en) * 1998-01-29 2000-01-25 Kumiai Chem Ind Co Ltd Diaryl sulfide derivative and pest controlling agent
EA200000840A1 (en) 1998-02-17 2001-02-26 Туларик, Инк. ANTI-VIRUS DERIVATIVES OF PYRIMIDINE
WO1999047154A1 (en) 1998-03-16 1999-09-23 Cytovia, Inc. Dipeptide caspase inhibitors and the use thereof
ID27600A (en) * 1998-06-02 2001-04-12 Osi Pharm Inc PIROLO COMPOSITION (2,3d) PYRIMIDINE AND ITS USE
WO1999065897A1 (en) 1998-06-19 1999-12-23 Chiron Corporation Inhibitors of glycogen synthase kinase 3
WO2000011003A1 (en) * 1998-08-21 2000-03-02 Du Pont Pharmaceuticals Company ISOXAZOLO[4,5-d]PYRIMIDINES AS CRF ANTAGONISTS
US6184226B1 (en) 1998-08-28 2001-02-06 Scios Inc. Quinazoline derivatives as inhibitors of P-38 α
ATE294796T1 (en) * 1998-10-08 2005-05-15 Astrazeneca Ab QUINAZOLINE DERIVATIVES
GB9828511D0 (en) * 1998-12-24 1999-02-17 Zeneca Ltd Chemical compounds
DE69926914T2 (en) 1999-01-13 2006-06-29 Warner-Lambert Co. Llc 1-HETEROCYCLE SUBSTITUTED DIARYLAMINES
AU3441400A (en) 1999-03-29 2000-10-16 Uutech Limited Peptide
CN1221262C (en) 1999-03-30 2005-10-05 诺瓦提斯公司 Phthalazine derivatives for treating inflammatory diseases
JP2003502424A (en) 1999-06-17 2003-01-21 シオノギ バイオリサーチ コーポレイション Inhibitor of IL-12 production
GB9914258D0 (en) * 1999-06-18 1999-08-18 Celltech Therapeutics Ltd Chemical compounds
JP2001042764A (en) 1999-08-04 2001-02-16 Sony Corp Map display device
MY133159A (en) 1999-08-13 2007-10-31 Vertex Pharma Inhibitors of c-jun n-terminal kinases (jnk) and other protein kinases
WO2001025220A1 (en) 1999-10-07 2001-04-12 Amgen Inc. Triazine kinase inhibitors
ES2253266T3 (en) 1999-11-30 2006-06-01 Pfizer Products Inc. 2,4-DIAMINOPIRIMIDINE COMPOUNDS USED AS IMMUNOSUPPRESSORS.
EP1731520A1 (en) 1999-12-02 2006-12-13 OSI Pharmaceuticals, Inc. Pyrrolo[2,3-d]pyrimidine derivatives which are antagonists of adenosine A1, A2A, and A3
US6376489B1 (en) 1999-12-23 2002-04-23 Icos Corporation Cyclic AMP-specific phosphodiesterase inhibitors
MY125768A (en) 1999-12-15 2006-08-30 Bristol Myers Squibb Co N-[5-[[[5-alkyl-2-oxazolyl]methyl]thio]-2-thiazolyl]-carboxamide inhibitors of cyclin dependent kinases
AU2457201A (en) 1999-12-28 2001-07-09 Bristol-Myers Squibb Company Cytokine, especially tnf-alpha, inhibitors
US20020065270A1 (en) * 1999-12-28 2002-05-30 Moriarty Kevin Joseph N-heterocyclic inhibitors of TNF-alpha expression
CN1362953A (en) * 2000-02-05 2002-08-07 沃泰克斯药物股份有限公司 Pyrazole compositions useful as inhibitors of ERK
HUP0301117A3 (en) * 2000-02-17 2004-01-28 Amgen Inc Thousand Oaks Imidazole derivatives kinase inhibitors, their use, process for their preparation and pharmaceutical compositions containing them
GB0004887D0 (en) * 2000-03-01 2000-04-19 Astrazeneca Uk Ltd Chemical compounds
GB0004890D0 (en) * 2000-03-01 2000-04-19 Astrazeneca Uk Ltd Chemical compounds
WO2001074768A2 (en) 2000-04-03 2001-10-11 Vertex Pharmaceuticals Incorporated Inhibitors of serine proteases, particularly hepatitis c virus ns3 protease
MXPA02010222A (en) 2000-04-18 2003-05-23 Agouron Pharma Pyrazoles for inhibiting protein kinase.
PL360439A1 (en) * 2000-06-28 2004-09-06 Astrazeneca Ab Substituted quinazoline derivatives and their use as inhibitors
WO2002008244A2 (en) 2000-07-21 2002-01-31 Schering Corporation Peptides as ns3-serine protease inhibitors of hepatitis c virus
CN1518543A (en) 2000-08-31 2004-08-04 �Ʒ� Pyrazole derivatives and their use as protein kinase inhibitors
US6610677B2 (en) * 2000-09-15 2003-08-26 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
US6613776B2 (en) * 2000-09-15 2003-09-02 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
US6660731B2 (en) * 2000-09-15 2003-12-09 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
IL154710A0 (en) * 2000-09-15 2003-10-31 Vertex Pharma Isoxazole derivatives and pharmaceutical compositions containing the same
US7473691B2 (en) * 2000-09-15 2009-01-06 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
EP1317449B1 (en) 2000-09-15 2006-05-31 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
MXPA03002410A (en) 2000-09-20 2003-06-19 Merck Patent Gmbh 4-amino-quinazolines.
US6716851B2 (en) * 2000-12-12 2004-04-06 Cytovia, Inc. Substituted 2-aryl-4-arylaminopyrimidines and analogs as activators or caspases and inducers of apoptosis and the use thereof
DE10061863A1 (en) * 2000-12-12 2002-06-13 Basf Ag Preparation of triethylenediamine, useful for making pharmaceuticals and polymers, by reacting ethylenediamine over specific zeolite catalyst
EP1351691A4 (en) 2000-12-12 2005-06-22 Cytovia Inc Substituted 2-aryl-4-arylaminopyrimidines and analogs as activators of caspases and inducers of apoptosis and the use thereof
ES2265450T3 (en) * 2000-12-21 2007-02-16 Vertex Pharmaceuticals Incorporated PIRAZOL COMPOUNDS USED AS INHIBITORS OF PROTEIN QUINASA.
MY130778A (en) * 2001-02-09 2007-07-31 Vertex Pharma Heterocyclic inhibitiors of erk2 and uses thereof
ES2292753T4 (en) * 2001-03-29 2009-02-16 Vertex Pharmaceuticals Incorporated INHIBITORS OF N-TERMINAL KINASES C-JUN (JNK) AND OTHER PROTEIN KINASES.
EP1389206B1 (en) * 2001-04-13 2006-09-13 Vertex Pharmaceuticals Incorporated Inhibitors of c-jun n-terminal kinases (jnk) and other protein kinases
EP1383771A1 (en) * 2001-04-20 2004-01-28 Vertex Pharmaceuticals Incorporated 9-deazaguanine derivatives as inhibitors of gsk-3
JP4316893B2 (en) * 2001-05-16 2009-08-19 バーテックス ファーマシューティカルズ インコーポレイテッド Inhibitors of Src and other protein kinases
MXPA03010961A (en) * 2001-05-31 2004-02-27 Vertex Pharma Thiazole compounds useful as inhibitors of protein kinases.
JP4523271B2 (en) * 2001-06-01 2010-08-11 バーテックス ファーマシューティカルズ インコーポレイテッド Thiazole compounds useful as inhibitors of protein kinases
MXPA03011652A (en) * 2001-06-15 2004-05-31 Vertex Pharma 5-(2-aminopyrimidin-4-yl) benzisoxazoles as protein kinase inhibitors.
ATE337312T1 (en) 2001-07-03 2006-09-15 Vertex Pharma ISOXAZOLYL PYRIMIDINES AS INHIBITORS OF SRC AND LCK PROTEIN KINASES
WO2003011287A1 (en) * 2001-08-03 2003-02-13 Vertex Pharmaceuticals Incorporated Pyrazolon derivatives as inhibitors of gsk-3
CA2469316A1 (en) * 2001-12-07 2003-06-19 Vertex Pharmaceuticals, Inc. Pyrimidine-based compounds useful as gsk-3 inhibitors
AU2003215087B2 (en) * 2002-02-06 2009-07-16 Vertex Pharmaceuticals Incorporated Heteroaryl compounds useful as inhibitors of GSK-3
WO2003078423A1 (en) * 2002-03-15 2003-09-25 Vertex Pharmaceuticals, Inc. Compositions useful as inhibitors of protein kinases
DE60332433D1 (en) * 2002-03-15 2010-06-17 Vertex Pharma AZOLYLAMINOAZINE AS PROTEIN KINASE INHIBITOR
WO2003078426A1 (en) * 2002-03-15 2003-09-25 Vertex Pharmaceuticals, Inc. Azolylaminoazine as inhibitors of protein kinases
DE60332604D1 (en) 2002-03-15 2010-07-01 Vertex Pharma AZOLYLAMINOAZINE AS PROTEIN KINASE INHIBITOR
US7863282B2 (en) 2003-03-14 2011-01-04 Vertex Pharmaceuticals Incorporated Compositions useful as inhibitors of protein kinases
US20030207873A1 (en) * 2002-04-10 2003-11-06 Edmund Harrington Inhibitors of Src and other protein kinases
EP1506189A1 (en) * 2002-04-26 2005-02-16 Vertex Pharmaceuticals Incorporated Pyrrole derivatives as inhibitors of erk2 and uses thereof
MY141867A (en) 2002-06-20 2010-07-16 Vertex Pharma Substituted pyrimidines useful as protein kinase inhibitors
WO2004005283A1 (en) * 2002-07-09 2004-01-15 Vertex Pharmaceuticals Incorporated Imidazoles, oxazoles and thiazoles with protein kinase inhibiting activities
ES2273043T3 (en) 2002-08-02 2007-05-01 Vertex Pharmaceuticals Incorporated PIRAZOL COMPOSITIONS USEFUL AS INHIBITORS OF GSK-3.
JP4688498B2 (en) * 2002-11-04 2011-05-25 バーテックス ファーマシューティカルズ インコーポレイテッド Heteroaryl-pyrimidine derivatives as JAK inhibitors
CA2515132C (en) * 2003-02-07 2012-01-03 Vertex Pharmaceuticals Incorporated Heteroaryl substituted pyrroles useful as inhibitors of protein kinases
ATE396731T1 (en) * 2003-03-25 2008-06-15 Vertex Pharma THIAZOLES FOR USE AS INHIBITORS OF PROTEIN KINASES
JP2006524688A (en) * 2003-03-25 2006-11-02 バーテックス　ファーマシューティカルズ　インコーポレイテッド Thiazoles useful as protein kinase inhibitors
DE602004022187D1 (en) 2003-10-17 2009-09-03 Astrazeneca Ab 4- (PYRAZOL-3-YLAMINO) PYRIMIDINE DERIVATIVES FOR USE IN THE TREATMENT OF CANCER
JP4329649B2 (en) 2004-08-30 2009-09-09 ソニー株式会社 Imaging apparatus and optical system driving method
EP1917259B1 (en) 2005-08-18 2012-01-25 Vertex Pharmaceuticals Incorporated Pyrazine kinase inhibitors
WO2007023382A2 (en) 2005-08-25 2007-03-01 Pfizer Inc. Pyrimidine amino pyrazole compounds, potent kinase inhibitors
EP1928456B1 (en) 2005-09-30 2015-04-22 Miikana Therapeutics, Inc. Substituted pyrazole compounds
BRPI0619704A2 (en) 2005-11-03 2011-10-11 Vertex Pharma compound, composition, method for inhibiting aurora kinase activity in a biological sample, method for treating a proliferative disorder and method for treating cancer
EP1951716B1 (en) 2005-11-16 2011-05-04 Vertex Pharmaceuticals, Inc. Aminopyrimidines useful as kinase inhibitors
JP2010509231A (en) 2006-11-02 2010-03-25 バーテックス ファーマシューティカルズ インコーポレイテッド Aminopyridines and aminopyrimidines useful as inhibitors of protein kinases
CA2673353A1 (en) 2006-12-19 2008-06-26 Vertex Pharmaceuticals Incorporated Aminopyrimidines useful as inhibitors of protein kinases
WO2008112651A2 (en) 2007-03-09 2008-09-18 Vertex Pharmaceuticals Incorporated Aminopyrimidines useful as inhibitors of protein kinases
CA2679884A1 (en) 2007-03-09 2008-09-18 Vertex Pharmaceuticals Incorporated Aminopyrimidines useful as inhibitors of protein kinases
EP2134709A1 (en) 2007-03-09 2009-12-23 Vertex Pharmaceuticals, Inc. Aminopyridines useful as inhibitors of protein kinases
WO2008115973A2 (en) 2007-03-20 2008-09-25 Vertex Pharmaceuticals Incorporated Aminopyrimidines useful as kinase inhibitors
EP2148931A2 (en) 2007-04-17 2010-02-03 Vertex Pharmaceuticals Incorporated Drug discovery methods for aurora kinase inhibitors
MX2009011810A (en) 2007-05-02 2010-01-14 Vertex Pharma Thiazoles and pyrazoles useful as kinase inhibitors.
WO2008137621A1 (en) 2007-05-02 2008-11-13 Vertex Pharmaceuticals Incorporated Aminopyrimidines useful as kinase inhibitors
MX2009011811A (en) 2007-05-02 2010-01-14 Vertex Pharma Aminopyrimidines useful as kinase inhibitors.
JP2010528021A (en) 2007-05-24 2010-08-19 バーテックス ファーマシューティカルズ インコーポレイテッド Thiazoles and pyrazoles useful as kinase inhibitors

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