Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
  • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
  • C07D498/04—Ortho-condensed systems
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01H—NEW PLANTS OR NON-TRANSGENIC PROCESSES FOR OBTAINING THEM; PLANT REPRODUCTION BY TISSUE CULTURE TECHNIQUES
  • A01H6/00—Angiosperms, i.e. flowering plants, characterised by their botanic taxonomy
  • A01H6/36—Ericaceae, e.g. azalea, cranberry or blueberry
  • A01H6/368—Vaccinium, e.g. cranberry, blueberry
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
  • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
  • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
  • A61K31/5375—1,4-Oxazines, e.g. morpholine
  • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
  • A61K31/5375—1,4-Oxazines, e.g. morpholine
  • A61K31/5383—1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with heterocyclic ring systems
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
  • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
  • A61P35/04—Antineoplastic agents specific for metastasis
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
  • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
  • C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
  • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
  • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Definitions

• the invention relates to substituted benzylindazole compounds, a process for their production and the use thereof.
• the eukaryotic cell division cycle ensures the duplication of the genome and its distribution to the daughter cells by passing through a coordinated and regulated sequence of events.
• the cell cycle is divided into four successive phases:
• the G1 phase represents the time before the DNA replication, in which the cell grows and is sensitive to external stimuli. 2. In the S phase the cell replicates its DNA, and 3. in the G2 phase preparations are made for entry into mitosis. 4. In mitosis (M phase), the duplicated chromosomes get separated supported by a spindle device built from microtubules, and cell division into two daughter cells is completed.
• the passage through the cell cycle is strictly regulated and controlled.
• the enzymes that are necessary for the progression through the cycle must be activated at the correct time and are also turned off again as soon as the corresponding phase is passed.
• Corresponding control points (“checkpoints”) stop or delay the progression through the cell cycle if DNA damage is detected, or the DNA replication or the creation of the spindle device is not yet completed.
• the mitotic checkpoint also known as spindle checkpoint or spindle assembly checkpoint
• the mitotic checkpoint is active as long as unattached kinetochores are present and generates a wait-signal to give the dividing cell the time to ensure that each kinetochore is attached to a spindle pole, and to correct attachment errors.
• the mitotic checkpoint prevents a mitotic cell from completing cell division with unattached or erroneously attached chromosomes [Suijkerbuijk S J and Kops G J, Biochem. Biophys. Acta 1786, 24, 2008; Musacchio A and Salmon E D, Nat. Rev. Mol. Cell. Biol. 8, 379, 2007].
• the mitotic checkpoint is established by a complex network of a number of essential proteins, including members of the MAD (mitotic arrest deficient, MAD 1-3) and Bub (Budding uninhibited by benzimidazole, Bub 1-3) families, Mps1 kinase, cdc20, as well as other components [reviewed in Bolanos-Garcia V M and Blundell T L, Trends Biochem. Sci. 36, 141, 2010], many of these being over-expressed in proliferating cells (e.g. cancer cells) and tissues [Yuan B et al., Clin. Cancer Res. 12, 405, 2006].
• the major function of an unsatisfied mitotic checkpoint is to keep the anaphase-promoting complex/cyclosome (APC/C) in an inactive state.
• APC/C anaphase-promoting complex/cyclosome
• ubiquitin-ligase targets cyclin B and securin for proteolytic degradation leading to separation of the paired chromosomes and exit from mitosis.
• Bub1 is one of the first mitotic checkpoint proteins that binds to the kinetochores of duplicated chromosomes and probably acts as a scaffolding protein to constitute the mitotic checkpoint complex. Furthermore, via phosphorylation of histone H2A, Bub1 localizes the protein shugoshin to the centromeric region of the chromosomes to prevent premature segregation of the paired chromosomes [Kawashima et al. Science 327, 172, 2010]. In addition, together with a Thr-3 phosphorylated Histone H3 the shugoshin protein functions as a binding site for the chromosomal passenger complex which includes the proteins survivin, borealin, INCENP and Aurora B.
• the chromosomal passenger complex is seen as a tension sensor within the mitotic checkpoint mechanism, which dissolves erroneously formed microtubule-kinetochor attachments such as syntelic (both sister kinetochore are attached to one spindle pole) or merotelic (one kinetochor is attached to two spindle poles) attachments [Watanabe Y, Cold Spring Harb. Symp. Quant. Biol. 75, 419, 2010].
• mitotic checkpoint abrogation through pharmacological inhibition of components of the mitotic checkpoint represents a new approach for the treatment of proliferative disorders, including solid tumours such as carcinomas, sarcomas, leukaemias and lymphoid malignancies or other disorders, associated with uncontrolled cellular proliferation.
• the present invention relates to chemical compounds that inhibit Bub1 kinase.
• Established anti-mitotic drugs such as vinca alkaloids, taxanes or epothilones activate the mitotic checkpoint, inducing a mitotic arrest either by stabilising or destabilising microtubule dynamics. This arrest prevents separation of the duplicated chromosomes to form the two daughter cells. Prolonged arrest in mitosis forces a cell either into mitotic exit without cytokinesis (mitotic slippage or adaption) or into mitotic catastrophe leading to cell death [Rieder C L and Maiato H, Dev. Cell 7, 637, 2004]. In contrast, inhibitors of Bub1 prevent the establishment and/or functionality of the mitotic checkpoint, which finally results in severe chromosomal missegregation, induction of apoptosis and cell death.
• Bub1 inhibitors should be of therapeutic value for the treatment of proliferative disorders associated with enhanced uncontrolled proliferative cellular processes such as, for example, cancer, inflammation, arthritis, viral diseases, cardiovascular diseases, or fungal diseases in a warm-blooded animal such as man.
• inhibitors of Bub1 represent valuable compounds that should complement therapeutic options either as single agents or in combination with other drugs.
• the invention relates to compounds of formula (I)
• the invention relates to compounds of formula (I)
• Another aspect of the invention are compounds of formula (I) according to claim 1 , wherein
• a further aspect of the invention are compounds of formula (I) according to claim 1 , wherein
• Another aspect of the invention are compounds of formula (I) according to claim 1 , wherein
• a further aspect of the invention are compounds of formula (I) according to claim 1 , wherein
• a further aspect of the invention are compounds of formula (I) according to claim 1 , wherein
• a further aspect of the invention are compounds of formula (I) according to claim 1 , compounds of formula (I) according to claim 1 ,
• a further aspect of the invention are compounds of formula (I) according to claim 1 , wherein
• a further aspect of the invention are compounds of formula (I) according to claim 1 , wherein
• R 1 is hydrogen
• R 2 /R 3 is independently fluorine, chlorine, bromine, cyano, CF3, or —O—CH2-CF3,
• R 4 is independently of each other hydrogen, fluorine, chlorine, bromine or iodine, cyano, —CH 3 , —C 3 H 9 , cyclopropyl, 1-propenyl, —CF 3 , —CH 2 —OH, —CH 2 —CH 2 —OH, —C(CH 3 ) 2 —OH, —CH 2 —C(CH 3 ) 2 —OH, —C(CH 3 ) 2 —CH 2 —OH, —OCH 3 , —OCF 3 , —OCF 2 H, —OCH 2 CF 3 , —C(O)CH 3 , —COOH, —C(O)OCH 3 , —C(O)OC 2 H 5 , —C(O)OC(CH 3 ) 3 ,
• R 7 is hydrogen, methyl, difluoromethyl, hydroxyethyl
• R 8 is hydrogen, fluorine, cyano, C(O)NH 2 , m is 0, 1 or 2
• R 9 is hydrogen, methyl, ethyl, tert.-butyl, hydroxyethyl, R 10 /R 11 is independently from each other hydrogen, methyl, hydroxyethyl, or an N-oxide, a salt, a
• a further aspect of the invention are compounds of formula (I) according to claim 1 ,
• a further aspect of the invention are compounds of formula (I) according to claim 1 , wherein
• a further aspect of the invention are compounds of formula (I) according to claim 1 , wherein
• R 7 is NH—C(O)OC(CH 3 ) 3 ,
• R 1 is hydrogen
• R 2 /R 3 is independently from each other hydrogen, fluorine, chlorine,
• R 4 is —O-(1-4C-alkyl), (2-4C-alkyl)-OH, 3-5C-cycloalkyl, 2-3C-alkenyl,
• * is the point of attachment, —O-(2-3C-alkyl)-NH 2 , —O—(CH 2 )heterocyclyl (which optionally is substituted with oxo ( ⁇ O) or C(O)OR 9 ), —O-(1-3C-alkyl), —O-(2-3C-alkyl)-OH, —O-(2-3C-alkyl)-SO-(2-3C-alkyl), —O-(2-3C-alkyl)-SO 2 -(2-3C-alkyl), —O-(2-3Calkyl)-SO 2 NH 2 , —O—(CH 2 )—CH(OH)—(CH 2 )-heterocyclyl, —O—(CH 2 )—CH(OH)—(CH 2 )—OH, —O—(CH 2 )—C(O)NR 10 R 11 , R 7 is hydrogen
• R 8 is hydrogen, C(O)NR 10 R 11
• a further aspect of the invention are compounds of formula (I) according to claim 1 , wherein
• R 1 is hydrogen
• R 2 /R 3 is independently from each other hydrogen, fluorine, chlorine
• R 4 is —O—CH 2 —CH 3 , CH 2 —OH, C(CH 3 ) 3 —OH, cyclopropyl, propenyl, —O—C(CH 3 ) 3 ,
• compounds of formula (I) as described above are selected from the group consisting of:
• compounds of formula (I) as described above are selected from the group consisting of:
• One aspect of the invention are compounds of formula (I) as described in the examples as characterized by their names in the title as claimed in claim 5 and their structures as well as the subcombinations of all residues specifically disclosed in the compounds of the examples.
• Another aspect of the present invention are the intermediates as used for their synthesis.
• One special aspect of the invention is intermediate (1-5) wherein,
• R 1 , R 6 , R 7 , R 8 and m have the meaning according to claim 1 .
• R 1 is hydrogen, halogen, 1-3C-alkyl
• R 1 is halogen
• R 1 is 1-3C-alkyl.
• a further aspect of the invention are compounds of formula (I), wherein
• R 1 is hydrogen, 1-3C-alkyl.
• a further aspect of the invention are compounds of formula (I), wherein
• R 2 /R 3 are independently from each other hydrogen, halogen, cyano, hydroxy 1-6C-haloalkyl, 1-6C-haloalkoxy, 1-6C-alkoxy,
• a further aspect of the invention are compounds of formula (I) according to claim 1 , wherein R 2 and/or R 3 are independently from each other hydrogen, halogen, cyano, 1-6C-haloalkyl, 1-6C-haloalkoxy.
• R 2 and/or R 3 is halogen, especially fluorine, chlorine or bromine, preferably fluorine or chlorine.
• R 2 and/or R 3 is 1-3C-haloalkyl, especially CF 3 .
• R 2 and/or R 3 is 1-3C-haloalkoxy, especially —O—CH 2 —CF 3 .
• R 2 and/or R 3 is fluorine, chlorine, bromine, CF 3 , or —O—CH 2 —CF 3 .
• R 2 and/or R 3 is fluorine, chlorine, bromine, hydroxy, methoxy, CF 3 , or —O—CH 2 —CF 3 .
• R 2 and R 3 are halogen or 1-3C-haloalkoxy, especially fluorine, chlorine, or —O—CH 2 —CF 3 .
• R 3 are hydroxy, (1-6C-alkoxy).
• a further aspect of the invention are compounds of formula (I), wherein
• R 2 and R 3 are different.
• Another aspect of the invention are compounds of formula (I), wherein one position of R 2 and R 3 is hydrogen and the other is halogen, 1-3C-haloalkyl, 1-3C-haloalkoxy or especially fluorine, chlorine, bromine, CF 3 , or —O—CH 2 —CF 3 .
• R 4 is independently hydrogen, hydroxy, halogen, cyano, NO 2 , 1-6C-alkyl, 2-6C-alkenyl, 2-6C-alkynyl, 1-6C-haloalkyl, 1-6C-hydroxyalkyl, 1-6C-alkoxy, —O-(2-6Calkylen)-O—C(O)-(1-6C-alkyl), 1-6C-haloalkoxy, —C(O)OR 9 , -(1-6C-alkylen)-C(O)OR 9 , —C(O)-(1-6C-alkyl), —C(O)NR 10 R 11 , 3-7C-cycloalkyl, —S-(1-6C-haloalkyl), SF 5 , —SO 2 NH-(3-7C-cycloalkyl), —SO 2 NR 10 R 11 , NR 10 R 11 , heteroaryl which optionally is substituted independently one or more times with cyano,
• R 4 is hydrogen
• R 4 is hydrogen or halogen, especially hydrogen or fluorine.
• R 4 is selected from the group consisting of hydroxy, NO 2 or NR 10 R 11 .
• R 4 is selected from the group consisting of is independently hydrogen, halogen, cyano, 1-6C-alkyl, 2-6C-alkenyl, 1-6C-haloalkyl, 1-6C-hydroxyalkyl, 1-6C-alkoxy, 1-6C-haloalkoxy, —C(O)OR 9 , -(1-6C-alkylen)-C(O)OR 9 , —C(O)-(1-6C-alkyl), —C(O)NR 10 R 11 , 3-7C-cycloalkyl, —S-(1-6C-haloalkyl), SF 5 , —SO 2 NH-(3-7C-cycloalkyl), —SO 2 NR 10 R 11 , heteroaryl which optionally is substituted independently one or more times with cyano, 1-4C-alkyl, 1-6C-haloalkyl, 1-6C-haloalkoxy, C(O)OR 9 , C(O)NR 10 R 11
• R 4 is selected from the group consisting of hydrogen, halogen, cyano, 1-3C-alkyl, 3-6C-cycloalkyl, 2-3C-alkenyl, 1-3C-haloalkyl, 1-3C-hydroxyalkyl, 1-3C-alkoxy, 1-3C-haloalkoxy, —C(O)-(1-3C-alkyl), COOH, (1-3C-alkylen)-COOH, -(1-3C-alkylen)-COO-(1-3C-alkyl), —COO-(1-4C-alkyl), —C(O)NH 2 , —C(O)NH(1-3C-alkyl), —C(O)N(1-3C-alkyl) 2 , —C(O)NH-(1-3C-alkyl)-OH, —C(O)—(N-heterocyclyl), —SO 2 —NH-(3-6C-cycloalkyl), —SO 2 —(
• R 4 is selected from the group consisting of hydrogen, hydroxy, fluorine, chlorine, bromine or iodine, cyano, nitro, —CH 3 , —C 3 H 9 , cyclopropyl, 1-propenyl, —CF 3 , —CH 2 —OH, —CH 2 —CH 2 —OH, —C(CH 3 ) 2 —OH, —CH 2 —C(CH 3 ) 2 —OH, —C(CH 3 ) 2 —CH 2 —OH, —OCH 3 , —OCF 3 , —OCF 2 H, —OCH 2 CF 3 , —C(O)CH 3 , —COOH, —C(O)OCH 3 , —C(O)OC 2 H 5 , —C(O)OC(CH 3 ) 3 , —CH 2 —COOC 2 H 5 , —CH 2 —COOH, —C(CH 3 ) 2 —
• R 4 is selected from the group consisting of hydrogen, fluorine, chlorine, bromine or iodine, cyano, —CH 3 , —C 3 H 9 , cyclopropyl, 1-propenyl, —CF 3 , —CH 2 —OH, —CH 2 —CH 2 —OH, —C(CH 3 ) 2 —OH, —CH 2 —C(CH 3 ) 2 —OH, —C(CH 3 ) 2 —CH 2 —OH, —OCH 3 , —OCF 3 , —OCF 2 H, —OCH 2 CF 3 , —C(O)CH 3 , —COOH, —C(O)OCH 3 , —C(O)OC 2 H 5 , —C(O)OC(CH 3 ) 3 , —CH2-COOC 2 H 5 , —CH 2 —COOH, —C(CH 3 ) 2 —COOC 2 H 5 ,
• a further aspect of the invention are compounds of formula (I), wherein whereby two of R 2 , R 3 (R 4 ) n , when positioned ortho to each other, may form together with the two carbon atoms to which they are attached, a heterocyclic 5-, 6- or 7-membered ring containing 1 or 2 heteroatoms selected from O or N, and optionally an additional double bond and/or a carbonyl group and/or an 1-4C-alkyl group, especially whereby two of R 2 , R 3 (R 4 ) n , when positioned ortho to each other, form together with the two carbon atoms to which they are attached, —O—CH 2 —CH 2 —CH 2 —O—, —O—CH 2 —CH 2 —, —(CH 3 )C ⁇ CH—(C ⁇ O)—O—, —CH 2 —(C ⁇ O)—O—, —(CH 2 ) 2 —(C ⁇ O)—NH—.
• the invention relates to compounds of formula (I), wherein n is 0, 1 or 2.
• n is at least 1.
• n 1.
• R 6 is (a) hydrogen; (b) hydroxy; (c) cyano; (d) 1-6C-alkoxy optionally substituted independently one or more times with
• a further aspect of the invention are compounds of formula (I), wherein
• R 6 is 1-6C-alkoxy which is optionally substituted independently one or more times.
• a further aspect of the invention are compounds of formula (I), wherein
• R 6 is 1-6C-alkoxy which is optionally substituted independently one or more times with
• R 6 is 1-6C-alkoxy which is optionally substituted independently one or more times with
• R 6 is (a) hydrogen
• R 6 is hydrogen, hydroxy, cyano, —O-(3-6C-cycloalkyl), 1-3C-alkoxy, 1-3C-haloalkoxy, —O-(1-3C-alkylen)-OH, —O-(1-3C-alkylen)-NH2, —O-(1-3C-alkylen)-NH(1-3C-alkyl), —O-(1-3C-alkylen)-N(1-3C-alkyl)2, —O-(1-3C-alkylen)-SO2NH2, —O-(1-3C-alkylen)-SO2N(1-3C-alkyl)2, —O-(1-3C-alkylen)-(optionally substituted heteroaryl), —C(O)NH2, —C(O)N(1-3C-alkyl)2.
• Another aspect of the invention are compounds of formula (I), wherein.
• R 6 is hydrogen, hydroxy, cyano, —O-cyclopropyl, —OCH 3 , —OCF 3 , —OCF 2 H, —OCH 2 CF 3 , —O—(CH 2 ) 2 —OH, —O—(CH 2 ) 2 —NH 2 , —O(CH 2 ) 2 —N(CH 3 ) 2 , —O—(CH 2 ) 2 —O—CH3, —O—(CH 2 ) 2 —O—(CH 2 ) 2 —OH, —O—CH 2 —CH(OH)—CH 2 OH, —O—CH 2 —CH(OH)—CH 2 —NH—C(O)OC(CH 3 ) 3 , —O—CH 2 —COOH, —O—CH 2 —COOC 2 H 5 , C(O)NH 2 , —O—CH 2 —C(O)-(3-fluoro-N-azetidine),
• R 6 is hydrogen, hydroxy, cyano, —O-cyclopropyl, —OCH 3 , —OCF 3 , —OCF 2 H, —OCH 2 CF 3 , —O—(CH 2 ) 2 —OH, —O(CH 2 ) 2 —N(CH 3 ) 2 , —O—CH 2 —SO 2 NH 2 ,
• R 6 is hydrogen, hydroxy, cyano, —O-cyclopropyl, —OCH 3 , —OCF 3 , —OCF 2 H, —OCH 2 CF 3 , —O—(CH 2 ) 2 —OH, —O(CH 2 ) 2 —N(CH 3 ) 2 , —O—CH 2 —SO 2 NH 2 ,
• Another aspect of the invention are compounds of formula (I), wherein if R 6 is in the 5-position of the pyrimidine ring directly neighbouring the R 7 bearing amino substituent, R 6 together with R 7 is a 5 or 6-membered ring including the nitrogen atom of the amino substituent which may contain one further heteroatom selected from O, S or N and which in addition may be substituted with a carbonyl group or —CH 2 —OH or —NH—CHO.
• R 6 is —O-(3-6C-cycloalkyl), 1-3C-alkoxy, 1-3C-haloalkoxy, —O-(1-3C-alkylen)-OH, —O-(1-3C-alkylen)-NH2, —O-(1-3C-alkylen)-NH(1-3C-alkyl), —O-(1-3C-alkylen)-N(1-3C-alkyl) 2 , —O-(1-3C-alkylen)-SO2NH2, —O-(1-3C-alkylen)-SO2N(1-3C-alkyl) 2 , —O-(1-3C-alkylen)-(optionally substituted heteroaryl), especially —O-cyclopropyl, —OCH3, —OCF3, —OCF2H, —OCH2CF3, —O—(CH2)2-OH, —O(CH2)2-N(CH3)2, —O—CH2-SO2NH2,
• R 6 is hydrogen, hydroxy, cyano, —O-cyclopropyl, —O(1-3C-alkyl), —O-(1-3C-haloalkyl), —O-(1-3C-alkylen optionally substituted by a hydroxy group)-OH, —O(1-3C-alkylen optionally substituted by a hydroxy group)-NR 10 R 11 , —O-(1-3-alkylen)- ⁇ -(1-3C-alkyl), —O-(1-3C-alkylen)-O-(1-3C-alkyl)-OH, —O-(1-3C-alkylen)-COOR 9 , C(O)NR 10 R 11 , —O-(1-3C-alkylen)-C(O)-(heterocycyl optionally substituted 1 or two times by fluorine), —O-(1-3-alkylen)-(heterocyclyl optionally substituted by an oxo ( ⁇
• R 6 is —O-(3-6C-cycloalkyl), 1-3C-alkoxy, 1-3C-haloalkoxy, —O-(1-3C-alkylen)-OH, —O-(1-3C-alkylen)-NH 2 , —O-(1-3C-alkylen)-NH(1-3C-alkyl), —O-(1-3C-alkylen)-N(1-3C-alkyl) 2 , —O-(1-3C-alkylen)-SO 2 NH 2 , —O-(1-3C-alkylen)-SO 2 N(1-3C-alkyl) 2 , —O-(1-3C-alkylen)-(optionally substituted heteroaryl), especially —O-cyclopropyl, —OCH 3 , —OCF 3 , —OCF 2 H, —OCH 2 CF 3 , —O—(CH 2 ) 2 —OH, —O(CH 2 )
• a further aspect of the invention are compounds of formula (I), wherein
• R 6 is 1-6C-alkoxy which is substituted by —S-(1-6C-alkyl), —SO-(1-6C-alkyl) or —SO 2 -(1-6C-alkyl).
• a further aspect of the invention are compounds of formula (I), wherein
• R 6 is SO 2 NR 10 R 11 .
• R 6 is —C(O)NH 2 , —C(O)N(1-3C-alkyl) 2 or cyano especially —C(O)NH 2 .
• R 7 is hydrogen, 1-3C-alkyl, 1-3C-haloalkyl, -(1-3C-alkylen)-OH,
• R 7 is hydrogen, 1-3C-alkyl, 1-3C-haloalkyl, 1-3C-hydroxyalkyl,
• R 7 is hydrogen, methyl, difluoromethyl, hydroxyethyl
• R 7 is hydrogen, methyl, difluoromethyl, hydroxyethyl
• R 7 is optionally one or more times substituted benzyl, the substitutents selected from the group consisting of halogen (especially fluorine, chlorine), cyano, 1-3C-alkoxy (especially methoxy, ethoxy), 1-3C-haloalkoxy (especially —OCF 3 , —O—CF 2 H, —O—CH 2 —CF 3 ).
• halogen especially fluorine, chlorine
• cyano especially methoxy, ethoxy
• 1-3C-haloalkoxy especially —OCF 3 , —O—CF 2 H, —O—CH 2 —CF 3 .
• the benzyl group is substituted 1-, 2-, 3- or 4 times.
• R 8 is hydrogen, halogen, hydroxy, cyano, 1-6C-alkyl, 1-6C-hydroxyalkyl, 1-6C-haloalkyl, 1-6C-haloalkoxy, C(O)OR 9 , C(O)NR 10 R 11 ,
• R 8 is hydrogen, halogen, cyano, 1-6C-haloalkyl, 1-6C-haloalkoxy, C(O)OR 9 , C(O)NR 10 R 11 ,
• R 8 is hydroxy-(1-6C-alkyl).
• R 8 is hydrogen, fluorine, hydroxy, cyano, 1-3C-alkyl, 1-3C-haloalkyl, 1-3C-hydroxyalkyl, 1-3C-alkoxy, C(O)OR 9 , C(O)NR 10 R 11 , especially hydrogen, fluorine, hydroxy, cyano, methyl, CF 3 , methoxy, hydroxymethyl, COOH, COOCH 3 , COOC 2 H 5 , C(O)NH 2 , C(O)NHCH 3 .
• Still another aspect of the invention are compounds of formula (I), wherein m is 0.
• Another aspect of the invention are compounds of formula (I), wherein m is 0 or 1.
• Another aspect of the invention are compounds of formula (I), wherein m is selected from 0, 1 or 2.
• R 10 /R 11 is independently from each other hydrogen, 1-3C-alkyl, 1-3C-hydroxyalkyl, especially hydrogen, methyl, hydroxyethyl,
• R 10 , R 11 are independently from each other hydrogen, 1-4C-alkyl, 1-4C-hydroxyalkyl, 1-4C-alkoxy, —(CO)-(1-6C-alkyl) or together with the nitrogen atom to which they are attached form a 4-6-membered heterocyclic ring optionally containing one further heteroatom selected from the group consisting of O, S or N, which is optionally with 1-2 halogen atoms, especially fluorine atoms.
• R 10 , R 11 are independently from each other hydrogen, 1-4C-alkyl, 1-4C-hydroxyalkyl, 1-4C-alkoxy, or together with the nitrogen atom to which they are attached form a 5-6-membered heterocyclic ring optionally containing one further heteroatom selected from the group consisting of O, S or N.
• R 10 , R 11 form together with the nitrogen atom to which they are attached a 4-membered heterocyclic ring, which is optionally with 1-2 halogen atoms, especially fluorine atoms.
• a further aspect of the invention are compounds of formula (I), which are present as their salts, especially as their hydrochlorides.
• Another embodiment of the invention are the tautomeric forms of a hydroxypyridine which are defined to be encompassed by the claim, should the compound of formula I include such a hydroxypyridine:
• Another embodiment of the invention are compounds according to the claims as disclosed in the Claims section wherein the definitions are limited according to the preferred or more preferred definitions as disclosed below or specifically disclosed residues of the exemplified compounds and subcombinations thereof.
• An alkyl constituent being multiply substituted by halogen includes also a completely halogenated alkyl moiety such as e.g. CF 3 .
• a constituent be composed of more than one part, e.g. —O-(1-6Calkyl)-(3-7C-cycloalkyl)
• the position of a possible substituent can be at any of these parts at any suitable position.
• a hyphen at the beginning of the constituent marks the point of attachment to the rest of the molecule.
• the substitutent could be at any suitable position of the ring, also on a ring nitrogen atom if suitable.
• 1-6C-alkyl is a straight-chain or branched alkyl group having 1 to 6 carbon atoms. Examples are methyl, ethyl, n propyl, iso-propyl, n butyl, iso-butyl, sec-butyl and tert-butyl, pentyl, hexyl, preferably 1-4 carbon atoms (1-4C-alkyl), more preferably 1-3 carbon atoms (1-3C-alkyl).
• Other alkyl constituents mentioned herein having another number of carbon atoms shall be defined as mentioned above taking into account the different length of their chain.
• alkylene a bridging moiety between two other parts of the constituent which usually is called an “alkylene” moiety
• alkylene a bridging moiety between two other parts of the constituent which usually is called an “alkylene” moiety
• alkylene a bridging moiety between two other parts of the constituent which usually is called an “alkylene” moiety
• 2-6C-Alkenyl is a straight chain or branched alkenyl radical having 2 to 6 carbon atoms. Examples are the but-2-enyl, but-3-enyl (homoallyl), prop-1-enyl, prop-2-enyl (allyl) and the ethenyl (vinyl) radicals.
• “Mono- or di-1-4C-alkylamino” radicals contain in addition to the nitrogen atom, independently one or two of the above mentioned 1-4C-alkyl radicals. Examples are the methylamino, the ethylamino, the isopropylamino, the dimethylamino, the diethylamino and the diisopropylamino radical.
• Halogen within the meaning of the present invention is iodine, bromine, chlorine or fluorine, preferably “halogen” within the meaning of the present invention is chlorine or fluorine.
• 1-6C-Haloalkyl is a straight-chain or branched alkyl group having 1 to 6 carbon atoms in which at least one hydrogen is substituted by a halogen atom. Examples are chloromethyl or 2-bromoethyl.
• partially or completely fluorinated C1-C4-alkyl group the following partially or completely fluorinated groups are considered, for example: fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, 1,1-difluoroethyl, 1,2-difluoroethyl, 1,1,1-trifluoroethyl, tetrafluoroethyl, and pentafluoroethyl, whereby difluoromethyl, trifluoromethyl, or 1,1,1-trifluoroethyl are preferred. All possible partially or completely fluorinated 1-6C-alkyl groups are considered to be encompassed by the term 1-6C-haloalkyl.
• 1-6C-Hydroxyalkyl is a straight-chain or branched alkyl group having 1 to 6 carbon atoms in which at least one hydrogen atom is substituted by a hydroxy group. Examples are hydroxymethyl, 1-hydroxyethyl, 2-hydroxyethyl, 1,2-dihydroxyethyl, 3-hydroxypropyl, 2-hydroxypropyl, 2,3-dihydroxypropyl, 3-hydroxy-2-methyl-propyl, 2-hydroxy-2-methyl-propyl, 1-hydroxy-2-methyl-propyl.
• 1-6C-Alkoxy represents radicals, which in addition to the oxygen atom, contain a straight-chain or branched alkyl radical having 1 to 6 carbon atoms. Examples which may be mentioned are the hexoxy, pentoxy, butoxy, isobutoxy, sec-butoxy, tert-butoxy, propoxy, isopropoxy, ethoxy and methoxy radicals, preferred are methoxy, ethoxy, propoxy, isopropoxy.
• 1-6C-Haloalkoxy represents radicals, which in addition to the oxygen atom, contain a straight-chain or branched alkyl radical having 1 to 6 carbon atoms in which at least one hydrogen is substituted by a halogen atom. Examples are —O—CFH2, —O—CF2H, —O—CF3, —O—CH2-CFH2, —O—CH2-CF2H, —O—CH2-CF3. Preferred are —O—CF2H, —O—CF3, —O—CH2-CF3.
• 3-7C-Cycloalkyl stands for cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl, preferably cyclopropyl.
• 3-7C-Cycloalkyloxy or “—O-(3-7C-cycloalkyl)” stands for e.g. cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, cyclohexyloxy or cycloheptyloxy, preferably cyclopropyloxy.
• heterocyclyl represents a mono- or polycyclic, preferably mono- or bicyclic, more preferably monocyclic, nonaromatic heterocyclic radical containing, 4 to 10, preferably 4 to 7, more preferably 5 to 6 ring atoms, and 1,2 or 3, preferably 1 or 2, hetero atoms and/or hetero groups independently selected from the series consisting of N, O, S, SO, SO 2 .
• the heterocyclyl radicals can be saturated or partially unsaturated and, unless stated otherwise, may be optionally substituted, one or more times, identically or differently, with a substituent selected from: 1-4C-alkyl, 1-4C-haloalkyl, 1-4C-alkoxy, hydroxy, fluorine or ( ⁇ O) whereby the 1-4C-alkyl may be optionally further substituted with hydroxy and the double bonded oxygen atom leads to a carbonyl group together with the carbon atom of the heterocyclyl ring at any suitable position.
• heterocyclic radicals are 4- to 7-membered monocyclic saturated heterocyclyl radicals having up to two hetero atoms from the series consisting of O, N and S, more preferred 5-6-membered heterocyclic radicals.
• the following may be mentioned by way of example and by preference: oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, azetidinyl, 3-hydroxyazetidinyl, 3-fluoroazetidinyl, 3,3-difluoroazetidinyl, pyrrolidinyl, 3-hydroxypyrrolidinyl, pyrrolinyl, pyrazolidinyl, imidazolidinyl, piperidinyl, 3-hydroxypiperidinyl, 4-hydroxypiperidinyl, 3-fluoropiperidinyl, 3,3-difluoropiperidinyl, 4-fluoropiperidinyl, 4,4-difluoropiperidinyl, pipe
• N-heterocyclyl represents a heterocyclic radical which is connected to the remaining molecule via its nitrogen atom contained in the heterocyclic ring.
• heteroaryl represents a monocyclic 5- or 6-membered aromatic heterocycle or a fused bicyclic aromatice moiety comprising without being restricted thereto, the 5-membered heteroaryl radicals furyl, thienyl, pyrrolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, imidazolyl, pyrazolyl, triazolyl (1,2,4-triazolyl, 1,3,4-triazolyl or 1,2,3-triazolyl), thiadiazolyl (1,3,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,2,3-thiadiazolyl or 1,2,4-thiadiazolyl) and oxadiazolyl (1,3,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,2,3-oxadiazolyl or 1,2,4-oxadiazolyl), as well as the 6-membered heteroaryl radicals pyr
• cumarinyl-, isocumarinyl-, indolizinyl-, isobenzofuranyl-, azaindolyl-, azaisoindolyl-, furanopyridyl-, furanopyrimidinyl-, furanopyrazinyl-, furanopyridazinyl-, preferred fused ring system is indazolyl.
• Preferred 5- or 6-membered heteroaryl radicals are furanyl, thienyl, pyrrolyl, thiazolyl, oxazolyl, thiadiazolyl, oxadiazolyl, pyridinyl, pyrimidinyl, pyrazinyl or pyridazinyl.
• More preferred 5- or 6-membered heteroaryl radicals are furan-2-yl, thien-2-yl, pyrrol-2-yl, thiazolyl, oxazolyl, 1,3,4-thiadiazolyl, 1,3,4-oxadiazolyl, pyridin-2-yl, pyridin-4-yl, pyrimidin-2-yl, pyrimidin-4-yl, pyrazin-2-yl or pyridazin-3-yl.
• the heteroarylic or heteroarylenic radicals include all the possible isomeric forms thereof, e.g. the positional isomers thereof.
• the term pyridinyl or pyridinylene includes pyridin-2-yl, pyridin-2-ylene, pyridin-3-yl, pyridin-3-ylene, pyridin-4-yl and pyridin-4-ylene; or the term thienyl or thienylene includes thien-2-yl, thien-2-ylene, thien-3-yl and thien-3-ylene.
• heteroarylic, heteroarylenic, or heterocyclic groups mentioned herein may be substituted by their given substituents or parent molecular groups, unless otherwise noted, at any possible position, such as e.g. at any substitutable ring carbon or ring nitrogen atom.
• any heteroaryl or heterocyclyl group may be attached to the rest of the molecule via any suitable atom if chemically suitable.
• any heteroatom of a heteroarylic or heteroarylenic ring with unsatisfied valences mentioned herein is assumed to have the hydrogen atom(s) to satisfy the valences.
• rings containing quaternizable amino- or imino-type ring nitrogen atoms may be preferably not quaternized on these amino- or imino-type ring nitrogen atoms by the mentioned substituents or parent molecular groups.
• the NR 10 R 11 group includes, for example, NH 2 , N(H)CH 3 , N(CH 3 ) 2 , N(H)CH 2 CH 3 and N(CH 3 )CH 2 CH 3 .
• —NR 10 R 11 when R 10 and R 11 together with the nitrogen atom to which they are attached form a 4-6-membered heterocyclic ring optionally containing one further heteroatom selected from the group consisting of O, S or N, the term “heterocyclic ring” is defined above. Especially preferred is morpholinyl.
• the C(O)NR 10 R 11 group includes, for example, C(O)NH 2 , C(O)N(H)CH 3 , C(O)N(CH 3 ) 2 , C(O)N(H)CH 2 CH 3 , C(O)N(CH 3 )CH 2 CH 3 or C(O)N(CH 2 CH 3 ) 2 .
• R 10 or R 11 are not hydrogen, they may be substituted by hydroxy,
• the term “heterocyclic ring” is defined above and can be used analogously for C(O)NR 10 R 11 .
• the C(O)OR 9 group includes for example C(O)OH, C(O)OCH 3 , C(O)OC 2 H 5 , C(O)C 3 H 7 , C(O)CH(CH 3 ) 2 , C(O)OC 4 H 9 , C(O)OC 5 H 11 , C(O)OC 6 H 13 ; for C(O)O(1-6Calkyl), the alkyl part may be straight or branched and may be substituted.
• pharmacokinetic profile means one single parameter or a combination thereof including permeability, bioavailability, exposure, and pharmacodynamic parameters such as duration, or magnitude of pharmacological effect, as measured in a suitable experiment.
• Compounds with improved pharmacokinetic profiles can, for example, be used in lower doses to achieve the same effect, may achieve a longer duration of action, or a may achieve a combination of both effects.
• Salts of the compounds according to the invention include all inorganic and organic acid addition salts and salts with bases, especially all pharmaceutically acceptable inorganic and organic acid addition salts and salts with bases, particularly all pharmaceutically acceptable inorganic and organic acid addition salts and salts with bases customarily used in pharmacy.
• salts of the compounds according to the invention including all inorganic and organic acid addition salts, especially all pharmaceutically acceptable inorganic and organic acid addition salts, particularly all pharmaceutically acceptable inorganic and organic acid addition salts customarily used in pharmacy.
• Another aspect of the invention are the salts with di- and tricarboxylic acids.
• acid addition salts include, but are not limited to, hydrochlorides, hydrobromides, phosphates, nitrates, sulfates, salts of sulfamic acid, formates, acetates, propionates, citrates, D-gluconates, benzoates, 2-(4-hydroxybenzoyl)-benzoates, butyrates, salicylates, sulfosalicylates, lactates, maleates, laurates, malates, fumarates, succinates, oxalates, malonates, pyruvates, acetoacetates, tartarates, stearates, benzenesulfonates, toluenesulfonates, methanesulfonates, trifluoromethansulfonates, 3-hydroxy-2-naphthoates, benzenesulfonates, naphthalinedisulfonates and trifluoroacetates.
• salts with bases include, but are not limited to, lithium, sodium, potassium, calcium, aluminum, magnesium, titanium, meglumine, ammonium, salts optionally derived from NH 3 or organic amines having from 1 to 16 C-atoms such as e.g. ethylamine, diethylamine, triethylamine, ethyldiisopropylamine, monoethanolamine, diethanolamine, triethanolamine, dicyclohexylamine, dimethylaminoethanol, procaine, dibenzylamine, N-methylmorpholine, arginine, lysine, ethylendiamine, N-methylpiperindine and guanidinium salts.
• organic amines having from 1 to 16 C-atoms such as e.g. ethylamine, diethylamine, triethylamine, ethyldiisopropylamine, monoethanolamine, diethanolamine, triethanolamine, dicyclohexylamine
• the salts include water-insoluble and, particularly, water-soluble salts.
• the compounds of formula (I) according to this invention as well as their salts may contain, e.g. when isolated in crystalline form, varying amounts of solvents. Included within the scope of the invention are therefore all solvates and in particular all hydrates of the compounds of formula (I) according to this invention as well as all solvates and in particular all hydrates of the salts of the compounds of formula (I) according to this invention.
• a “fixed combination” in the present invention is used as known to persons skilled in the art and is defined as a combination wherein the said first active ingredient and the said second active ingredient are present together in one unit dosage or in a single entity.
• a “fixed combination” is a pharmaceutical composition wherein the said first active ingredient and the said second active ingredient are present in admixture for simultaneous administration, such as in a formulation.
• Another example of a “fixed combination” is a pharmaceutical combination wherein the said first active ingredient and the said second active ingredient are present in one unit without being in admixture.
• a non-fixed combination or “kit-of-parts” in the present invention is used as known to persons skilled in the art and is defined as a combination wherein the said first active ingredient and the said second active ingredient are present in more than one unit.
• a non-fixed combination or kit-of-parts is a combination wherein the said first active ingredient and the said second active ingredient are present separately.
• the components of the non-fixed combination or kit-of-parts may be administered separately, sequentially, simultaneously, concurrently or chronologically staggered.
• (chemotherapeutic) anti-cancer agents includes but is not limited to 131I-chTNT, abarelix, abiraterone, aclarubicin, aldesleukin, alemtuzumab, alitretinoin, altretamine, aminoglutethimide, amrubicin, amsacrine, anastrozole, arglabin, arsenic trioxide, asparaginase, azacitidine, basiliximab, BAY 80-6946, BAY 1000394, belotecan, bendamustine, bevacizumab, bexarotene, bicalutamide, bisantrene, bleomycin, bortezomib, buserelin, busulfan, cabazitaxel, calcium folinate, calcium levofolinate, capecitabine, carboplatin, carmofur, carmustine, catumaxomab, celecoxib, celmol
• the compounds according to the invention and their salts can exist in the form of tautomers which are included in the embodiments of the invention.
• the compounds of the invention may, depending on their structure, exist in different stereoisomeric forms. These forms include configurational isomers or optionally conformational isomers (enantiomers and/or diastereoisomers including those of atropisomers).
• the present invention therefore includes enantiomers, diastereoisomers as well as mixtures thereof. From those mixtures of enantiomers and/or diastereoisomers pure stereoisomeric forms can be isolated with methods known in the art, preferably methods of chromatography, especially high pressure liquid chromatography (HPLC) using achiral or chiral phase.
• HPLC high pressure liquid chromatography
• the invention further includes all mixtures of the stereoisomers mentioned above independent of the ratio, including the racemates.
• bioprecursors or pro-drugs are covered by the invention.
• Said biological system is e.g. a mammalian organism, particularly a human subject.
• the bioprecursor is, for example, converted into the compound of formula (I) or a salt thereof by metabolic processes.
• said compounds of the present invention have surprisingly been found to effectively inhibit Bub1 kinase and may therefore be used for the treatment or prophylaxis of diseases of uncontrolled cell growth, proliferation and/or survival, inappropriate cellular immune responses, or inappropriate cellular inflammatory responses or diseases which are accompanied with uncontrolled cell growth, proliferation and/or survival, inappropriate cellular immune responses, or inappropriate cellular inflammatory responses, particularly in which the uncontrolled cell growth, proliferation and/or survival, inappropriate cellular immune responses, or inappropriate cellular inflammatory responses is mediated by Bub1 kinase, such as, for example, haemotological tumours, solid tumours, and/or metastases thereof, e.g.
• leukaemias and myelodysplastic syndrome including leukaemias and myelodysplastic syndrome, malignant lymphomas, head and neck tumours including brain tumours and brain metastases, tumours of the thorax including non-small cell and small cell lung tumours, gastrointestinal tumours, endocrine tumours, mammary and other gynaecological tumours, urological tumours including renal, bladder and prostate tumours, skin tumours, and sarcomas, and/or metastases thereof.
• R 1 , R 2 , R 3 , R 4 , R 6 , R 8 , m and n have the meaning as given for general formula (I), supra.
• interconversion of any of the substituents, R 1 , R 2 , R 3 , R 4 , R 6 or R 8 can be achieved before and/or after the exemplified transformations. These modifications can be such as the introduction of protecting groups, cleavage of protecting groups, reduction or oxidation of functional groups, halogenation, metallation, substitution or other reactions known to the person skilled in the art. These transformations include those which introduce a functionality which allows for further interconversion of substituents.
• X represents a leaving group such as for example a Cl, Br or I, or X stands for an aryl sulfonate such as for example p-toluene sulfonate, or for an alkyl sulfonate such as for example methane sulfonate or trifluoromethane sulfonate.
• X′ represents F, Cl, Br, I, boronic acid or a boronic acid ester, such as for example 4,4,5,5-tetramethyl-2-phenyl-1,3,2-dioxaborolane (boronic acid pinacole ester).
• a suitably substituted 1H-indazole-3-carbonitrile (A) can be reacted with a suitably substituted benzyl halide or benzyl sulfonate of general formula (B), such as, for example, a benzyl bromide, in a suitable solvent system, such as, for example, N,N-dimethylformamide, in the presence of a suitable base, such as, for example, cesium carbonate at temperatures ranging from ⁇ 78° C. to room temperature, preferably the reaction is carried out at room temperature, to furnish 1-benzyl-1H-indazole-3-carbonitrile intermediates of general formula (1-1).
• a suitably substituted benzyl halide or benzyl sulfonate of general formula (B) such as, for example, a benzyl bromide
• a suitable solvent system such as, for example, N,N-dimethylformamide
• a suitable base such as, for example, cesium carbonate
• Intermediates of general formula (1-1) can be converted to intermediates of general formula (1-2) by reaction with a suitable alcoholate, such as, for example sodium methanolate, in a suitable solvent system, such as, for example, the corresponding alcohol, e.g. methanol, at a temperature between room temperature and the boiling point of the respective solvent, preferably the reaction is carried out at room temperature, and subsequent treatment with a suitable source of ammonium, such as for example, ammonium chloride in the presence of a suitable acid, such as for example acetic acid in a temperature range from room temperature to the boiling point of the respective solvent, preferably the reaction is carried out at 50° C.
• a suitable alcoholate such as, for example sodium methanolate
• a suitable solvent system such as, for example, the corresponding alcohol, e.g. methanol
• Intermediates of general formula (1-4) can be reacted with a suitable 4-halopyridine of the general formula (C), such as, for example 4-bromopyridine, in the presence of a suitable base, such as, for example sodium 2-methylpropan-2-olate or potassium carbonate.
• a suitable palladium catalyst such as for example (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one-palladium
• a suitable ligand such as for example 1′-binaphthalene-2,2′-diylbis(diphenylphosphane
• reaction is carried out in a suitable solvent system, such as, for example, N,N-dimethylformamide, in a temperature range from room temperature to the boiling point of the respective solvent, preferably the reaction is carried out at 100° C. to furnish compounds of general formula (Ia).
• a suitable solvent system such as, for example, N,N-dimethylformamide
• the reaction is carried out at 100° C. to furnish compounds of general formula (Ia).
• the following palladium catalysts can be used:
• Allylpalladium chloride dimer Dichlorobis(benzonitrile)palladium (II), Palladium (II) acetate, Palladium (II) chloride, Tetrakis(triphenylphosphine)palladium (0), Tris(dibenzylideneacetone)dipalladium (0), optionally with addition of the following ligands: racemic-2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl, rac-BINAP, 1,1′-Bis(diphenylphosphino)ferrocene, Bis(2-diphenylphosphinophenyl)ether, Di-t-butylmethylphosphonium tetrafluoroborate, 2-(Di-t-butylphosphino)biphenyl, Tri-t-butylphosphonium tetrafluoroborate, Tri-2-furylphosphine, Tris(2,4-
• intermediates of general formula (1-4) can be reacted with a suitable boronic acid or boronic acid pinacole ester of general formula (C), such as, for example (2-fluoropyridin-4-yl)boronic acid, in the presence of a suitable base, such as, for example triethylamine, a suitable activating agent such as for example N,N-dimethylpyridin-4-amine and a suitable copper salt, such as for example copper (II) acetate, in a suitable solvent system, such as, for example, trichloromethane, in a temperature range from room temperature to the boiling point of the respective solvent, preferably the reaction is carried out at room temperature to furnish compounds of general formula (Ia).
• a suitable boronic acid or boronic acid pinacole ester of general formula (C) such as, for example (2-fluoropyridin-4-yl)boronic acid
• a suitable base such as, for example triethylamine
• a suitable activating agent
• intermediates of general formula (1-4) can be reacted with a suitable pyridyl fluoride of general formula (C, with X′ being F), such as, for example 4-fluoro pyridine hydrochloride, in the presence of a suitable base, such as, for example sodium hydride, in a suitable solvent system, such as, for example, dimethyl formamide, in a temperature range from room temperature to the boiling point of the respective solvent, preferably the reaction is carried out at 90° C. to furnish compounds of general formula (Ia).
• a suitable pyridyl fluoride of general formula (C, with X′ being F) such as, for example 4-fluoro pyridine hydrochloride
• a suitable base such as, for example sodium hydride
• solvent system such as, for example, dimethyl formamide
• R 1 , R 2 , R 3 , R 4 , R 6 , R 7 , R 8 , m and n have the meaning as given for general formula (I), supra.
• R′ is for example alkyl or benzyl, preferably methyl or ethyl.
• interconversion of any of the substituents, R 1 , R 2 , R 3 , R 4 , R 6 , R 7 or R 8 can be achieved before and/or after the exemplified transformations.
• These modifications can be such as the introduction of protecting groups, cleavage of protecting groups, reduction or oxidation of functional groups, halogenation, metallation, substitution or other reactions known to the person skilled in the art.
• Compounds of general formula (Ib) are converted to intermediates of general formula (1-5) by treatment with a suitable acid system, such as, for example a mixture of trifluoroacetic acid and trifluoromethanesulfonic acid, in a suitable solvent, such as, for example, dichloroethan, in a temperature range from room temperature to the boiling point of the respective solvent, preferably the reaction is carried out at room temperature.
• a suitable acid system such as, for example a mixture of trifluoroacetic acid and trifluoromethanesulfonic acid
• a suitable solvent such as, for example, dichloroethan
• Intermediates of general formula (1-5) can be reacted with a suitably substituted benzyl halide or benzyl sulfonate of general formula (B), such as, for example, a benzyl bromide, in a suitable solvent system, such as, for example, tetrahydrofuran, in the presence of a suitable base, such as, for example, sodium hydride in a temperature range from room temperature to the boiling point of the respective solvent, preferably the reaction is carried out at room temperature, to furnish compounds of general formula (I).
• Said reaction can also result in double conversion of intermediate (1-5) if R 7 is hydrogen, giving rise to compounds formed alongside the target compounds, in which R 7 is a benzylic group identical with the benzylic moiety attached to the indazole nitrogen.
• a suitable protecting group such as, for example, tert-butoxycarbonyl with a suitable reagent, such as, for example, di-tert-butyldicarbonate, in the presence of a suitable base, such as, for example, sodium hydroxide in water, in a suitable solvent system, such as, for example, methanol in a temperature range from 0° C. to room temperature, preferable the reaction is carried out at room temperature, to furnish compounds of general formula (1-8).
• a suitable protecting group such as, for example, tert-butoxycarbonyl with a suitable reagent, such as, for example, di-tert-butyldicarbonate
• a suitable base such as, for example, sodium hydroxide in water
• a suitable solvent system such as, for example, methanol in a temperature range from 0° C. to room temperature, preferable the reaction is carried out at room temperature, to furnish compounds of general formula (1-8).
• Intermediates of general formula (1-8) can be protected with a suitable protection group such as, for example, allyloxycarbonyl or benzoyl with a suitable reagent, such as, for example, allyl chloroformate or benzoyl chloride, in a suitable solvent system, such as, for example, pyridine, in a temperature range from room temperature to the boiling point of the respective solvent, preferably the reaction is carried out at room temperature, to furnish compounds of general formula (1-9).
• a suitable protection group such as, for example, allyloxycarbonyl or benzoyl
• a suitable reagent such as, for example, allyl chloroformate or benzoyl chloride
• solvent system such as, for example, pyridine
• X represents leaving group such as for example a Cl, Br or I
• X stands for an aryl sulfonate such as for example p-toluene sulfonate, or for an alkyl sulfonate such as for example methane sulfonate or trifluoromethane sulfonate (triflate group).
• R′′ 1-6C-alkyl (independently one or more times optionally substituted with hydroxy, C(O)OR 9 , C(O)NR 10 R 11 , NR 10 R 11 , —S-(1-6C-alkyl), —S(O)-(1-6C-alkyl), —S(O) 2 -(1-6C-alkyl), SO 2 NR 10 R 11 , heterocyclyl (which itself is optionally substituted with C(O)OR 9 or oxo ( ⁇ O)), heteroaryl (which itself is optionally substituted one or more times with cyano, 1-4C-alkyl, 1-6C-haloalkyl, 1-6C-haloalkoxy, C(O)OR 9 , C(O)NR 10 R 11 , -(2-6C-alkyl)-O-1-6C-alkyl), 3-7C-cycloalkyl, halogen, or
• Compounds of general formula (Ic) are converted to compounds of general formula (Id) by treatment with a suitable demethylating agent, such as for example benzenethiol, in a suitable solvent, such as, for example, 1-methylpyrrolidin-2-one, in the presence of a suitable base, such as, for example potassium carbonate, in a temperature range from room temperature to the boiling point of the respective solvent, preferably the reaction is carried out at 190° C.
• a suitable demethylating agent such as for example benzenethiol
• a suitable solvent such as, for example, 1-methylpyrrolidin-2-one
• a suitable base such as, for example potassium carbonate
• step 2 of this sequence the residues might potentially undergo a modification, e.g. reduction.
• O—R′′′ represents a suitable leaving group, e.g. a triflate group, nonaflate group.
• Compounds of general formula (Id) can be converted to intermediates of general formula (I-6) by reaction with a suitable sulfonic acid derivative, such as, for example trifluoromethanesulfonic anhydride or 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonyl fluoride, in a suitable solvent, such as, for example, dichloromethane, in the presence of a suitable base, such as, for example pyridine, in a temperature range from room temperature to the boiling point of the respective solvent, preferably the reaction is carried out at room temperature.
• a suitable sulfonic acid derivative such as, for example trifluoromethanesulfonic anhydride or 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonyl fluoride
• a suitable solvent such as, for example, dichloromethane
• a suitable base such as, for example pyridine
• R 7a represents 1-6C-alkyl, independently one or more times optionally substituted with heteroaryl, halogen, hydroxy, or R 7a stands for
• R 7a represents benzyl, whereby the phenyl ring is opt. subst with 1-5 substituents independently selected from the group consisting of hydrogen, halogen, 1-4Calkyl, 1-4C-haloalkyl, 1-4C-alkoxy, 1-4C-haloalkoxy, cyano, C(O)OR 9 .
• X as defined below scheme 1, supra, or for example 1,3,2-dioxathiolane 2-oxide.
• R 7b represents an acyl moiety, such as —C(O)-(1-6C-alkyl), —C(O)-(1-6C-alkylen)-O-(1-6C-alkyl), —C(O)-(1-6C-alkylen)-O-(2-6C-alkylen)-O-(1-6C-alkyl), —C(O)-heterocyclyl and Z represents a halogen, hydroxy or —O—R 7b .
• Compounds of general formula (If′) are converted into compounds of general formula (Ig) by reaction with a suitable haloalkyl or dioxathiolane 2-oxide, such as, for example 1, 3,2-dioxathiolane 2-oxide, in a suitable solvent system, such as, for example, N,N-dimethyl formamide, in the presence of a suitable base, such as, for example cesium carbonate, in a temperature range from room temperature to the boiling point of the respective solvent, preferably the reaction is carried out at 60° C.
• a suitable haloalkyl or dioxathiolane 2-oxide such as, for example 1, 3,2-dioxathiolane 2-oxide
• a suitable solvent system such as, for example, N,N-dimethyl formamide
• a suitable base such as, for example cesium carbonate
• Compounds of general formula (If′) are converted into compounds of general formula (Ih) by reaction with a suitable carboxylic acid derivative, such as for example a carboxylic acid halogenide e.g. carboxylic acid chloride, or a carboxylic acid anhydride, in a suitable solvent, such as, for example, dichloromethane, in the presence of a suitable base, such as, for example N,N-diethylethanamine, in a temperature range from room temperature to the boiling point of the respective solvent, preferably the reaction is carried out at room temperature.
• a suitable carboxylic acid derivative such as for example a carboxylic acid halogenide e.g. carboxylic acid chloride, or a carboxylic acid anhydride
• a suitable solvent such as, for example, dichloromethane
• a suitable base such as, for example N,N-diethylethanamine
• R 1 , R 2 , R 3 , R 4 , R 8 , m and n have the meaning as given for general formula (I), supra.
• interconversion of any of the substituents, R 1 , R 2 , R 3 , R 4 or R 8 can be achieved before and/or after the exemplified transformations. These modifications can be such as the introduction of protecting groups, cleavage of protecting groups, reduction or oxidation of functional groups, halogenation, metallation, substitution or other reactions known to the person skilled in the art. These transformations include those which introduce a functionality which allows for further interconversion of substituents.
• a suitably substituted carboximidamide or its respective hydrochloride of general formula (1-2), such as for example, 1-(2-fluorobenzyl)-1H-indazole-3-carboximidamide hydrochloride (1:1), can be reacted with dimethyl (methoxymethylidene)-propanedioate (E), in a suitable solvent system, such as, for example, methanol, in the presence of a suitable base, such as, for example, sodium methanolate at temperatures ranging from room temperature to the boiling point of the solvent, preferably the reaction is carried out at 60° C., to furnish intermediates of general formula (1-12).
• a suitable solvent system such as, for example, methanol
• a suitable base such as, for example, sodium methanolate
• Intermediates of general formula (1-12) can be converted to intermediates of general formula (1-13) by reaction with a suitable source of ammonia, such as, for example 7N ammonia, in a suitable solvent system, such as, for example methanol, at temperatures ranging from room temperature to the boiling point of the solvent, preferably the reaction is carried out at 60° C., to furnish intermediates of general formula (1-13).
• a suitable source of ammonia such as, for example 7N ammonia
• a suitable solvent system such as, for example methanol
• Intermediates of general formula (1-13) can be converted to intermediates of general formula (1-14) by reaction with a suitable source of chloride, such as, for example phosphoric trichloride, neat, in the presence of a suitable base, such as, for example, N,N-diethylaniline, at temperatures ranging from room temperature to the boiling point of the solvent, preferably the reaction is carried out at 90° C., to furnish intermediates of general formula (1-14).
• a suitable source of chloride such as, for example phosphoric trichloride
• a suitable base such as, for example, N,N-diethylaniline
• Intermediates of general formula (1-14) can be converted to intermediates of general formula (II) by reaction with a suitably substituted pyridin-4-amine, such as, for example pyridin-4-amine, in a suitable solvent system, such as, for example N,N-dimethylformamide, at temperatures ranging from room temperature to the boiling point of the solvent, preferably the reaction is carried out at room temperature, to furnish compounds of general formula (Ii).
• a suitably substituted pyridin-4-amine such as, for example pyridin-4-amine
• a suitable solvent system such as, for example N,N-dimethylformamide
• Compounds of general formula (Ii) can be converted into compounds of general formula (Ij) by treatment with a suitable acid, such as, for example concentrated sulfuric acid, at temperatures ranging from 0° C. to room temperature, preferably the reaction is carried out at room temperature, to furnish compounds of general formula (Ij).
• a suitable acid such as, for example concentrated sulfuric acid
• One preferred aspect of the invention is the process for the preparation of the compounds of claims 1 - 6 according to the Examples.
• a special aspect of the present invention are the following two process steps:
• R 1 , R 2 , R 3 , R 6 , R 7 , R 8 and m have the meaning according to claim 1 and R′ is 1-6C-alkyl or benzyl, is treated with a suitable acid system to cleave the benzylic group in order to obtain a compound of formula 1-5
• R 2 , R 3 , R 4 and n have the meaning according to claim 1
• X represents a leaving group, in a suitable solvent system, in the presence of a suitable base, in a temperature range from room temperature to the boiling point of the respective solvent, to furnish compounds of general formula (I).
• Another aspect of the invention is the intermediate of general formula (1-5).
• the compounds according to the invention are isolated and purified in a manner known per se, e.g. by distilling off the solvent in vacuo and recrystallizing the residue obtained from a suitable solvent or subjecting it to one of the customary purification methods, such as chromatography on a suitable support material.
• reverse phase preparative HPLC of compounds of the present invention which possess a sufficiently basic or acidic functionality may result in the formation of a salt, such as, in the case of a compound of the present invention which is sufficiently basic, a trifluoroacetate or formate salt for example, or, in the case of a compound of the present invention which is sufficiently acidic, an ammonium salt for example.
• Salts of this type can either be transformed into its free base or free acid form, respectively, by various methods known to the person skilled in the art, or be used as salts in subsequent biological assays. Additionally, the drying process during the isolation of compounds of the present invention may not fully remove traces of cosolvents, especially such as formic acid or trifluoroacetic acid, to give solvates or inclusion complexes. The person skilled in the art will recognise which solvates or inclusion complexes are acceptable to be used in subsequent biological assays. It is to be understood that the specific form (e.g. salt, free base, solvate, inclusion complex) of a compound of the present invention as isolated as described herein is not necessarily the only form in which said compound can be applied to a biological assay in order to quantify the specific biological activity.
• Salts of the compounds of formula (I) according to the invention can be obtained by dissolving the free compound in a suitable solvent (for example a ketone such as acetone, methylethylketone or methylisobutylketone, an ether such as diethyl ether, tetrahydrofuran or dioxane, a chlorinated hydrocarbon such as methylene chloride or chloroform, or a low molecular weight aliphatic alcohol such as methanol, ethanol or isopropanol) which contains the desired acid or base, or to which the desired acid or base is then added.
• a suitable solvent for example a ketone such as acetone, methylethylketone or methylisobutylketone, an ether such as diethyl ether, tetrahydrofuran or dioxane, a chlorinated hydrocarbon such as methylene chloride or chloroform, or a low molecular weight aliphatic alcohol
• the acid or base can be employed in salt preparation, depending on whether a mono- or polybasic acid or base is concerned and depending on which salt is desired, in an equimolar quantitative ratio or one differing therefrom.
• the salts are obtained by filtering, reprecipitating, precipitating with a non-solvent for the salt or by evaporating the solvent. Salts obtained can be converted into the free compounds which, in turn, can be converted into salts.
• pharmaceutically unacceptable salts which can be obtained, for example, as process products in the manufacturing on an industrial scale, can be converted into pharmaceutically acceptable salts by processes known to the person skilled in the art.
• hydrochlorides and the process used in the example section are especially preferred.
• Pure diastereomers and pure enantiomers of the compounds and salts according to the invention can be obtained e.g. by asymmetric synthesis, by using chiral starting compounds in synthesis and by splitting up enantiomeric and diasteriomeric mixtures obtained in synthesis.
• Enantiomeric and diastereomeric mixtures can be split up into the pure enantiomers and pure diastereomers by methods known to a person skilled in the art. Preferably, diastereomeric mixtures are separated by crystallization, in particular fractional crystallization, or chromatography. Enantiomeric mixtures can be separated e.g. by forming diastereomers with a chiral auxiliary agent, resolving the diastereomers obtained and removing the chiral auxiliary agent.
• chiral auxiliary agents for example, chiral acids can be used to separate enantiomeric bases such as e.g. mandelic acid and chiral bases can be used to separate enantiomeric acids via formation of diastereomeric salts.
• diastereomeric derivatives such as diastereomeric esters can be formed from enantiomeric mixtures of alcohols or enantiomeric mixtures of acids, respectively, using chiral acids or chiral alcohols, respectively, as chiral auxiliary agents.
• diastereomeric complexes or diastereomeric clathrates may be used for separating enantiomeric mixtures.
• enantiomeric mixtures can be split up using chiral separating columns in chromatography. Another suitable method for the isolation of enantiomers is the enzymatic separation.
• One preferred aspect of the invention is the process for the preparation of the compounds of claims 1 - 5 according to the examples.
• compounds of the formula (I) can be converted into their salts, or, optionally, salts of the compounds of the formula (I) can be converted into the free compounds.
• Corresponding processes are customary for the skilled person.
• N-oxides can be converted into their N-oxides.
• the N-oxide may also be introduced by way of an intermediate.
• N-oxides may be prepared by treating an appropriate precursor with an oxidizing agent, such as meta-chloroperbenzoic acid, in an appropriate solvent, such as dichloromethane, at suitable temperatures, such as from 0° C. to 40° C., whereby room temperature is generally preferred. Further corresponding processes for forming N-oxides are customary for the skilled person.
• the compounds of the present invention have surprisingly been found to effectively inhibit Bub1 finally resulting in apoptosis and cell death and may therefore be used for the treatment or prophylaxis of diseases of uncontrolled cell growth, proliferation and/or survival, inappropriate cellular immune responses, or inappropriate cellular inflammatory responses, or diseases which are accompanied with uncontrolled cell growth, proliferation and/or survival, inappropriate cellular immune responses, or inappropriate cellular inflammatory responses, particularly in which the uncontrolled cell growth, proliferation and/or survival, inappropriate cellular immune responses, or inappropriate cellular inflammatory responses is mediated by Bub1, such as, for example, benign and malignant neoplasia, more specifically haematological tumours, solid tumours, and/or metastases thereof, e.g.
• leukaemias and myelodysplastic syndrome including leukaemias and myelodysplastic syndrome, malignant lymphomas, head and neck tumours including brain tumours and brain metastases, tumours of the thorax including non-small cell and small cell lung tumours, gastrointestinal tumours, endocrine tumours, mammary and other gynaecological tumours, urological tumours including renal, bladder and prostate tumours, skin tumours, and sarcomas, and/or metastases thereof,
• endocrine glands e.g. thyroid and adrenal cortex
• Haematological tumors can e.g be exemplified by aggressive and indolent forms of leukemia and lymphoma, namely non-Hodgkins disease, chronic and acute myeloid leukemia (CML/AML), acute lymphoblastic leukemia (ALL), Hodgkins disease, multiple myeloma and T-cell lymphoma. Also included are myelodysplastic syndrome, plasma cell neoplasia, paraneoplastic syndromes, and cancers of unknown primary site as well as AIDS related malignancies.
• a further aspect of the invention is the use of the compounds according to formula (I) for the treatment of cer-vical-, breast-, non-small cell lung-, prostate-, colon- and melanoma tumors and/or metastases thereof, especially preferred for the treatment thereof as well as a method of treatment of cervical-, breast-, non-small cell lung-, prostate-, colon- and melanoma tumors and/or metastases thereof comprising administering an effective amount of a compound of formula (I).
• One aspect of the invention is the use of the compounds according to formula (I) for the treatment of cervix tumors as well as a method of treatment of cervix tumors comprising administering an effective amount of a compound of formula (I).
• the invention relates to a compound of general formula I, or an N-oxide, a salt, a tautomer or a stereoisomer of said compound, or a salt of said N-oxide, tautomer or stereoisomer particularly a pharmaceutically acceptable salt thereof, or a mixture of same, as described and defined herein, for use in the treatment or prophylaxis of a disease, especially for use in the treatment of a disease.
• Another particular aspect of the present invention is therefore the use of a compound of general formula I, described supra, or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, particularly a pharmaceutically acceptable salt thereof, or a mixture of same, for the prophylaxis or treatment of hyperproliferative disorders or disorders responsive to induction of apoptosis, especially for the treatment of hyperproliferative disorders or disorders responsive to induction of apoptosis.
• the use is in the treatment or prophylaxis of diseases, especially the treatment, wherein the diseases are haemotological tumours, solid tumours and/or metastases thereof.
• a preferred aspect is the use of a compound of formula (I) for the prophylaxis and/or treatment of cervical-, breast-, non-small cell lung-, prostate-, colon- and/or melanoma tumors, especially preferred for the treatment thereof.
• Another aspect is the use of a compound of formula (I) is for the treatment of cervical-, breast-, non-small cell lung-, prostate-, colon- and melanoma tumors and/or metastases thereof, especially preferred for the treatment thereof.
• the present invention relates to a method for using the compounds of the present invention and compositions thereof, to treat mammalian hyper-proliferative disorders.
• Compounds can be utilized to inhibit, block, reduce, decrease, etc., cell proliferation and/or cell division, and/or produce apoptosis.
• This method comprises administering to a mammal in need thereof, including a human, an amount of a compound of this invention, or a pharmaceutically acceptable salt, isomer, polymorph, metabolite, hydrate, solvate or ester thereof; etc. which is effective to treat the disorder.
• Hyper-proliferative disorders include but are not limited, e.g., psoriasis, keloids, and other hyperplasias affecting the skin, benign prostate hyperplasia (BPH), solid tumours, such as cancers of the breast, respiratory tract, brain, reproductive organs, digestive tract, urinary tract, eye, liver, skin, head and neck, thyroid, parathyroid and their distant metastases.
• BPH benign prostate hyperplasia
• solid tumours such as cancers of the breast, respiratory tract, brain, reproductive organs, digestive tract, urinary tract, eye, liver, skin, head and neck, thyroid, parathyroid and their distant metastases.
• Those disorders also include lymphomas, sarcomas, and leukaemias.
• breast cancer examples include, but are not limited to invasive ductal carcinoma, invasive lobular carcinoma, ductal carcinoma in situ, and lobular carcinoma in situ.
• cancers of the respiratory tract include, but are not limited to small-cell and non-small-cell lung carcinoma, as well as bronchial adenoma and pleuro-pulmonary blastoma.
• brain cancers include, but are not limited to brain stem and hypophtalmic glioma, cerebellar and cerebral astrocytoma, medulloblastoma, ependymoma, as well as neuroectodermal and pineal tumour.
• Tumours of the male reproductive organs include, but are not limited to prostate and testicular cancer.
• Tumours of the female reproductive organs include, but are not limited to endometrial, cervical, ovarian, vaginal, and vulvar cancer, as well as sarcoma of the uterus.
• Tumours of the urinary tract include, but are not limited to bladder, penile, kidney, renal pelvis, ureter, urethral and human papillary renal cancers.
• Eye cancers include, but are not limited to intraocular melanoma and retinoblastoma.
• liver cancers include, but are not limited to hepatocellular carcinoma (liver cell carcinomas with or without fibrolamellar variant), cholangiocarcinoma (intrahepatic bile duct carcinoma), and mixed hepatocellular cholangiocarcinoma.
• Skin cancers include, but are not limited to squamous cell carcinoma, Kaposi's sarcoma, malignant melanoma, Merkel cell skin cancer, and non-melanoma skin cancer.
• Head-and-neck cancers include, but are not limited to laryngeal, hypopharyngeal, nasopharyngeal, oropharyngeal cancer, lip and oral cavity cancer and squamous cell.
• Lymphomas include, but are not limited to AIDS-related lymphoma, non-Hodgkin's lymphoma, cutaneous T-cell lymphoma, Burkitt lymphoma, Hodgkin's disease, and lymphoma of the central nervous system.
• Sarcomas include, but are not limited to sarcoma of the soft tissue, osteosarcoma, malignant fibrous histiocytoma, lymphosarcoma, and rhabdomyosarcoma.
• Leukemias include, but are not limited to acute myeloid leukemia, acute lymphoblastic leukemia, chronic lymphocytic leukemia, chronic myelogenous leukemia, and hairy cell leukemia.
• treating or “treatment” as stated throughout this document is used conventionally, e.g., the management or care of a subject for the purpose of combating, alleviating, reducing, relieving, improving the condition of, etc., of a disease or disorder, such as a carcinoma.
• the present invention also provides methods for the treatment of disorders associated with aberrant mitogen extracellular kinase activity, including, but not limited to stroke, heart failure, hepatomegaly, cardiomegaly, diabetes, Alzheimer's disease, cystic fibrosis, symptoms of xenograft rejections, septic shock or asthma.
• Effective amounts of compounds of the present invention can be used to treat such disorders, including those diseases (e.g., cancer) mentioned in the Background section above. Nonetheless, such cancers and other diseases can be treated with compounds of the present invention, regardless of the mechanism of action and/or the relationship between the kinase and the disorder.
• aberrant kinase activity or “aberrant tyrosine kinase activity,” includes any abnormal expression or activity of the gene encoding the kinase or of the polypeptide it encodes. Examples of such aberrant activity, include, but are not limited to, over-expression of the gene or polypeptide; gene amplification; mutations which produce constitutively-active or hyperactive kinase activity; gene mutations, deletions, substitutions, additions, etc.
• the present invention also provides for methods of inhibiting a kinase activity, especially of mitogen extracellular kinase, comprising administering an effective amount of a compound of the present invention, including salts, polymorphs, metabolites, hydrates, solvates, prodrugs (e.g.: esters) thereof, and diastereoisomeric forms thereof.
• Kinase activity can be inhibited in cells (e.g., in vitro), or in the cells of a mammalian subject, especially a human patient in need of treatment.
• the present invention also provides methods of treating disorders and diseases associated with excessive and/or abnormal angiogenesis.
• Inappropriate and ectopic expression of angiogenesis can be deleterious to an organism.
• a number of pathological conditions are associated with the growth of extraneous blood vessels. These include, e.g., diabetic retinopathy, ischemic retinal-vein occlusion, and retinopathy of prematurity [Aiello et al. New Engl. J. Med. 1994, 331, 1480; Peer et al. Lab. Invest. 1995, 72, 638], age-related macular degeneration [AMD; see, Lopez et al. Invest. Opththalmol. Vis. Sci.
• neovascular glaucoma neovascular glaucoma, psoriasis, retrolental fibroplasias, angiofibroma, inflammation, rheumatoid arthritis (RA), restenosis, in-stent restenosis, vascular graft restenosis, etc.
• RA rheumatoid arthritis
• restenosis in-stent restenosis
• vascular graft restenosis etc.
• the increased blood supply associated with cancerous and neoplastic tissue encourages growth, leading to rapid tumour enlargement and metastasis.
• the growth of new blood and lymph vessels in a tumour provides an escape route for renegade cells, encouraging metastasis and the consequence spread of the cancer.
• compounds of the present invention can be utilized to treat and/or prevent any of the aforementioned angiogenesis disorders, e.g., by inhibiting and/or reducing blood vessel formation; by inhibiting, blocking, reducing, decreasing, etc. endothelial cell proliferation or other types involved in angiogenesis, as well as causing cell death or apoptosis of such cell types.
• the diseases of said method are haematological tumours, solid tumour and/or metastases thereof.
• the compounds of the present invention can be used in particular in therapy and prevention i.e. prophylaxis, especially in therapy of tumour growth and metastases, especially in solid tumours of all indications and stages with or without pre-treatment of the tumour growth.
• This invention also relates to pharmaceutical compositions containing one or more compounds of the present invention. These compositions can be utilised to achieve the desired pharmacological effect by administration to a patient in need thereof.
• a patient for the purpose of this invention, is a mammal, including a human, in need of treatment for the particular condition or disease.
• the present invention includes pharmaceutical compositions that are comprised of a pharmaceutically acceptable carrier or auxiliary and a pharmaceutically effective amount of a compound, or salt thereof, of the present invention.
• Another aspect of the invention is a pharmaceutical composition
• a pharmaceutical composition comprising a pharmaceutically effective amount of a compound of formula (I) and a pharmaceutically acceptable auxiliary for the treatment of a disease mentioned supra, especially for the treatment of haemotological tumours, solid tumours and/or metastases thereof.
• a pharmaceutically acceptable carrier or auxiliary is preferably a carrier that is non-toxic and innocuous to a patient at concentrations consistent with effective activity of the active ingredient so that any side effects ascribable to the carrier do not vitiate the beneficial effects of the active ingredient.
• Carriers and auxiliaries are all kinds of additives assisting to the composition to be suitable for administration.
• a pharmaceutically effective amount of compound is preferably that amount which produces a result or exerts the intended influence on the particular condition being treated.
• the compounds of the present invention can be administered with pharmaceutically-acceptable carriers or auxiliaries well known in the art using any effective conventional dosage unit forms, including immediate, slow and timed release preparations, orally, parenterally, topically, nasally, ophthalmically, optically, sublingually, rectally, vaginally, and the like.
• the compounds can be formulated into solid or liquid preparations such as capsules, pills, tablets, troches, lozenges, melts, powders, solutions, suspensions, or emulsions, and may be prepared according to methods known to the art for the manufacture of pharmaceutical compositions.
• the solid unit dosage forms can be a capsule that can be of the ordinary hard- or soft-shelled gelatine type containing auxiliaries, for example, surfactants, lubricants, and inert fillers such as lactose, sucrose, calcium phosphate, and corn starch.
• the compounds of this invention may be tableted with conventional tablet bases such as lactose, sucrose and cornstarch in combination with binders such as acacia, corn starch or gelatine, disintegrating agents intended to assist the break-up and dissolution of the tablet following administration such as potato starch, alginic acid, corn starch, and guar gum, gum tragacanth, acacia, lubricants intended to improve the flow of tablet granulation and to prevent the adhesion of tablet material to the surfaces of the tablet dies and punches, for example talc, stearic acid, or magnesium, calcium or zinc stearate, dyes, colouring agents, and flavouring agents such as peppermint, oil of wintergreen, or cherry flavouring, intended to enhance the aesthetic qualities of the tablets and make them more acceptable to the patient.
• binders such as acacia, corn starch or gelatine
• disintegrating agents intended to assist the break-up and dissolution of the tablet following administration such as potato starch, alginic acid
• Suitable excipients for use in oral liquid dosage forms include dicalcium phosphate and diluents such as water and alcohols, for example, ethanol, benzyl alcohol, and polyethylene alcohols, either with or without the addition of a pharmaceutically acceptable surfactant, suspending agent or emulsifying agent.
• Various other materials may be present as coatings or to otherwise modify the physical form of the dosage unit. For instance tablets, pills or capsules may be coated with shellac, sugar or both.
• Dispersible powders and granules are suitable for the preparation of an aqueous suspension. They provide the active ingredient in admixture with a dispersing or wetting agent, a suspending agent and one or more preservatives. Suitable dispersing or wetting agents and suspending agents are exemplified by those already mentioned above. Additional excipients, for example those sweetening, flavouring and colouring agents described above, may also be present.
• the pharmaceutical compositions of this invention may also be in the form of oil-in-water emulsions.
• the oily phase may be a vegetable oil such as liquid paraffin or a mixture of vegetable oils.
• Suitable emulsifying agents may be (1) naturally occurring gums such as gum acacia and gum tragacanth, (2) naturally occurring phosphatides such as soy bean and lecithin, (3) esters or partial esters derived form fatty acids and hexitol anhydrides, for example, sorbitan monooleate, (4) condensation products of said partial esters with ethylene oxide, for example, polyoxyethylene sorbitan monooleate.
• the emulsions may also contain sweetening and flavouring agents.
• Oily suspensions may be formulated by suspending the active ingredient in a vegetable oil such as, for example, arachis oil, olive oil, sesame oil or coconut oil, or in a mineral oil such as liquid paraffin.
• the oily suspensions may contain a thickening agent such as, for example, beeswax, hard paraffin, or cetyl alcohol.
• the suspensions may also contain one or more preservatives, for example, ethyl or n-propyl p-hydroxybenzoate; one or more colouring agents; one or more flavouring agents; and one or more sweetening agents such as sucrose or saccharin.
• Syrups and elixirs may be formulated with sweetening agents such as, for example, glycerol, propylene glycol, sorbitol or sucrose. Such formulations may also contain a demulcent, and preservative, such as methyl and propyl parabens and flavouring and colouring agents.
• the compounds of this invention may also be administered parenterally, that is, subcutaneously, intravenously, intraocularly, intrasynovially, intramuscularly, or interperitoneally, as injectable dosages of the compound in preferably a physiologically acceptable diluent with a pharmaceutical carrier which can be a sterile liquid or mixture of liquids such as water, saline, aqueous dextrose and related sugar solutions, an alcohol such as ethanol, isopropanol, or hexadecyl alcohol, glycols such as propylene glycol or polyethylene glycol, glycerol ketals such as 2,2-dimethyl-1,1-dioxolane-4-methanol, ethers such as poly(ethylene glycol) 400, an oil, a fatty acid, a fatty acid ester or, a fatty acid glyceride, or an acetylated fatty acid glyceride, with or without the addition of a pharmaceutically acceptable surfactant such
• Suitable fatty acids include oleic acid, stearic acid, isostearic acid and myristic acid.
• Suitable fatty acid esters are, for example, ethyl oleate and isopropyl myristate.
• Suitable soaps include fatty acid alkali metal, ammonium, and triethanolamine salts and suitable detergents include cationic detergents, for example dimethyl dialkyl ammonium halides, alkyl pyridinium halides, and alkylamine acetates; anionic detergents, for example, alkyl, aryl, and olefin sulfonates, alkyl, olefin, ether, and monoglyceride sulfates, and sulfosuccinates; non-ionic detergents, for example, fatty amine oxides, fatty acid alkanolamides, and poly(oxyethylene-oxypropylene)s or ethylene oxide or propylene oxide copolymers; and amphoteric detergents, for example, alkyl-beta-aminopropionates, and 2-alkylimidazoline quarternary ammonium salts, as well as mixtures.
• suitable detergents include cationic detergents, for example di
• compositions of this invention will typically contain from about 0.5% to about 25% by weight of the active ingredient in solution. Preservatives and buffers may also be used advantageously. In order to minimise or eliminate irritation at the site of injection, such compositions may contain a non-ionic surfactant having a hydrophile-lipophile balance (HLB) preferably of from about 12 to about 17. The quantity of surfactant in such formulation preferably ranges from about 5% to about 15% by weight.
• the surfactant can be a single component having the above HLB or can be a mixture of two or more components having the desired HLB.
• surfactants used in parenteral formulations are the class of polyethylene sorbitan fatty acid esters, for example, sorbitan monooleate and the high molecular weight adducts of ethylene oxide with a hydrophobic base, formed by the condensation of propylene oxide with propylene glycol.
• compositions may be in the form of sterile injectable aqueous suspensions.
• suspensions may be formulated according to known methods using suitable dispersing or wetting agents and suspending agents such as, for example, sodium carboxymethylcellulose, methylcellulose, hydroxypropylmethylcellulose, sodium alginate, polyvinylpyrrolidone, gum tragacanth and gum acacia; dispersing or wetting agents which may be a naturally occurring phosphatide such as lecithin, a condensation product of an alkylene oxide with a fatty acid, for example, polyoxyethylene stearate, a condensation product of ethylene oxide with a long chain aliphatic alcohol, for example, heptadeca-ethyleneoxycetanol, a condensation product of ethylene oxide with a partial ester derived form a fatty acid and a hexitol such as polyoxyethylene sorbitol monooleate, or a condensation product of an ethylene oxide with a partial ester derived from a fatty
• the sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally acceptable diluent or solvent.
• Diluents and solvents that may be employed are, for example, water, Ringer's solution, isotonic sodium chloride solutions and isotonic glucose solutions.
• sterile fixed oils are conventionally employed as solvents or suspending media.
• any bland, fixed oil may be employed including synthetic mono- or diglycerides.
• fatty acids such as oleic acid can be used in the preparation of injectables.
• composition of the invention may also be administered in the form of suppositories for rectal administration of the drug.
• These compositions can be prepared by mixing the drug with a suitable non-irritation excipient which is solid at ordinary temperatures but liquid at the rectal temperature and will therefore melt in the rectum to release the drug.
• suitable non-irritation excipient which is solid at ordinary temperatures but liquid at the rectal temperature and will therefore melt in the rectum to release the drug.
• suitable non-irritation excipient which is solid at ordinary temperatures but liquid at the rectal temperature and will therefore melt in the rectum to release the drug.
• Such materials are, for example, cocoa butter and polyethylene glycol.
• Controlled release formulations for parenteral administration include liposomal, polymeric microsphere and polymeric gel formulations that are known in the art.
• a mechanical delivery device It may be desirable or necessary to introduce the pharmaceutical composition to the patient via a mechanical delivery device.
• the construction and use of mechanical delivery devices for the delivery of pharmaceutical agents is well known in the art.
• Direct techniques for administration, for example, administering a drug directly to the brain usually involve placement of a drug delivery catheter into the patient's ventricular system to bypass the blood-brain barrier.
• One such implantable delivery system, used for the transport of agents to specific anatomical regions of the body is described in U.S. Pat. No. 5,011,472, issued Apr. 30, 1991.
• compositions of the invention can also contain other conventional pharmaceutically acceptable compounding ingredients, generally referred to as carriers or diluents, as necessary or desired.
• Conventional procedures for preparing such compositions in appropriate dosage forms can be utilized. Such ingredients and procedures include those described in the following references, each of which is incorporated herein by reference: Powell, M. F. et al., “Compendium of Excipients for Parenteral Formulations” PDA Journal of Pharmaceutical Science & Technology 1998, 52(5), 238-311; Strickley, R. G “Parenteral Formulations of Small Molecule Therapeutics Marketed in the United States (1999)—Part-1” PDA Journal of Pharmaceutical Science & Technology 1999, 53(6), 324-349; and Nema, S. et al., “Excipients and Their Use in Injectable Products” PDA Journal of Pharmaceutical Science & Technology 1997, 51(4), 166-171.
• compositions for its intended route of administration include:
• acidifying agents examples include but are not limited to acetic acid, citric acid, fumaric acid, hydrochloric acid, nitric acid
• alkalinizing agents examples include but are not limited to ammonia solution, ammonium carbonate, diethanolamine, monoethanolamine, potassium hydroxide, sodium borate, sodium carbonate, sodium hydroxide, triethanolamine, trolamine
• adsorbents examples include but are not limited to powdered cellulose and activated charcoal
• aerosol propellants examples include but are not limited to carbon dioxide, CCl 2 F 2 , F 2 ClC—CClF 2 and CClF 3
• air displacement agents examples include but are not limited to nitrogen and argon
• antifungal preservatives examples include but are not limited to benzoic acid, butylparaben, ethylparaben, methylparaben, propylparaben, sodium benzoate
• antimicrobial preservatives examples include but are not limited to benzoic acid, butylpara
• clarifying agents include but are not limited to bentonite
• emulsifying agents include but are not limited to acacia, cetomacrogol, cetyl alcohol, glyceryl monostearate, lecithin, sorbitan monooleate, polyoxyethylene 50 monostearate
• encapsulating agents include but are not limited to gelatin and cellulose acetate phthalate
• flavourants include but are not limited to anise oil, cinnamon oil, cocoa, menthol, orange oil, peppermint oil and vanillin
• humectants include but are not limited to glycerol, propylene glycol and sorbitol
• levigating agents include but are not
• compositions according to the present invention can be illustrated as follows:
• Sterile i.v. solution A 5 mg/mL solution of the desired compound of this invention can be made using sterile, injectable water, and the pH is adjusted if necessary. The solution is diluted for administration to 1-2 mg/mL with sterile 5% dextrose and is administered as an i.v. infusion over about 60 minutes.
• Lyophilised powder for i.v. administration A sterile preparation can be prepared with (i) 100-1000 mg of the desired compound of this invention as a lyophilised powder, (ii) 32-327 mg/mL sodium citrate, and (iii) 300-3000 mg Dextran 40.
• the formulation is reconstituted with sterile, injectable saline or dextrose 5% to a concentration of 10 to 20 mg/mL, which is further diluted with saline or dextrose 5% to 0.2-0.4 mg/mL, and is administered either IV bolus or by IV infusion over 15-60 minutes.
• Intramuscular suspension The following solution or suspension can be prepared, for intramuscular injection: 50 mg/mL of the desired, water-insoluble compound of this invention 5 mg/mL sodium carboxymethylcellulose 4 mg/mL TWEEN 80 9 mg/mL sodium chloride 9 mg/mL benzyl alcohol
• Hard Shell Capsules A large number of unit capsules are prepared by filling standard two-piece hard galantine capsules each with 100 mg of powdered active ingredient, 150 mg of lactose, 50 mg of cellulose and 6 mg of magnesium stearate.
• Soft Gelatin Capsules A mixture of active ingredient in a digestible oil such as soybean oil, cottonseed oil or olive oil is prepared and injected by means of a positive displacement pump into molten gelatin to form soft gelatin capsules containing 100 mg of the active ingredient. The capsules are washed and dried. The active ingredient can be dissolved in a mixture of polyethylene glycol, glycerin and sorbitol to prepare a water miscible medicine mix. Tablets: A large number of tablets are prepared by conventional procedures so that the dosage unit is 100 mg of active ingredient, 0.2 mg. of colloidal silicon dioxide, 5 mg of magnesium stearate, 275 mg of microcrystalline cellulose, 11 mg. of starch, and 98.8 mg of lactose.
• aqueous and non-aqueous coatings may be applied to increase palatability, improve elegance and stability or delay absorption.
• Immediate Release Tablets/Capsules These are solid oral dosage forms made by conventional and novel processes. These units are taken orally without water for immediate dissolution and delivery of the medication.
• the active ingredient is mixed in a liquid containing ingredient such as sugar, gelatin, pectin and sweeteners. These liquids are solidified into solid tablets or caplets by freeze drying and solid state extraction techniques.
• the drug compounds may be compressed with viscoelastic and thermoelastic sugars and polymers or effervescent components to produce porous matrices intended for immediate release, without the need of water.
• the effective dosage of the compounds of this invention can readily be determined for treatment of each desired indication.
• the amount of the active ingredient to be administered in the treatment of one of these conditions can vary widely according to such considerations as the particular compound and dosage unit employed, the mode of administration, the period of treatment, the age and sex of the patient treated, and the nature and extent of the condition treated.
• the total amount of the active ingredient to be administered will generally range from about 0.001 mg/kg to about 200 mg/kg body weight per day, and preferably from about 0.01 mg/kg to about 20 mg/kg body weight per day.
• Clinically useful dosing schedules will range from one to three times a day dosing to once every four weeks dosing.
• “drug holidays” in which a patient is not dosed with a drug for a certain period of time may be beneficial to the overall balance between pharmacological effect and tolerability.
• a unit dosage may contain from about 0.5 mg to about 1500 mg of active ingredient, and can be administered one or more times per day or less than once a day.
• the average daily dosage for administration by injection will preferably be from 0.01 to 200 mg/kg of total body weight.
• the average daily rectal dosage regimen will preferably be from 0.01 to 200 mg/kg of total body weight.
• the average daily vaginal dosage regimen will preferably be from 0.01 to 200 mg/kg of total body weight.
• the average daily topical dosage regimen will preferably be from 0.1 to 200 mg administered between one to four times daily.
• the transdermal concentration will preferably be that required to maintain a daily dose of from 0.01 to 200 mg/kg.
• the average daily inhalation dosage regimen will preferably be from 0.01 to 100 mg/kg of total body weight.
• the specific initial and continuing dosage regimen for each patient will vary according to the nature and severity of the condition as determined by the attending diagnostician, the activity of the specific compound employed, the age and general condition of the patient, time of administration, route of administration, rate of excretion of the drug, drug combinations, and the like.
• the desired mode of treatment and number of doses of a compound of the present invention or a pharmaceutically acceptable salt or ester or composition thereof can be ascertained by those skilled in the art using conventional treatment tests.
• the compounds of this invention can be administered as the sole pharmaceutical agent or in combination with one or more other pharmaceutical agents where the combination causes no unacceptable adverse effects.
• Those combined pharmaceutical agents can be other agents having antiproliferative effects such as for example for the treatment of haemotological tumours, solid tumours and/or metastases thereof and/or agents for the treatment of undesired side effects.
• the present invention relates also to such combinations.
• anti-hyper-proliferative agents suitable for use with the composition of the invention include but are not limited to those compounds acknowledged to be used in the treatment of neoplastic diseases in Goodman and Gilman's The Pharmacological Basis of Therapeutics (Ninth Edition), editor Molinoff et al., publ. by McGraw-Hill, pages 1225-1287, (1996), which is hereby incorporated by reference, especially (chemotherapeutic) anti-cancer agents as defined supra.
• the combination can be a non-fixed combination or a fixed-dose combination as the case may be.
• PDA Photo Diode Array PoraPak TM a HPLC column obtainable from Waters q quartet r.t. or rt room temperature RT retention time (as measured either with HPLC or UPLC) in minutes s singlet SM starting material SQD Single-Quadrupol-Detector t triplet THF tetrahydrofuran UPLC ultra performance liquid chromatography
• NMR peak forms in the following specific experimental descriptions are stated as they appear in the spectra, possible higher order effects have not been considered.
• Reactions employing microwave irradiation may be run with a Biotage Initator® microwave oven optionally equipped with a robotic unit.
• the reported reaction times employing microwave heating are intended to be understood as fixed reaction times after reaching the indicated reaction temperature.
• the compounds and intermediates produced according to the methods of the invention may require purification. Purification of organic compounds is well known to the person skilled in the art and there may be several ways of purifying the same compound. In some cases, no purification may be necessary. In some cases, the compounds may be purified by crystallization. In some cases, impurities may be stirred out using a suitable solvent.
• the compounds may be purified by chromatography, particularly flash column chromatography, using for example prepacked silica gel cartridges, e.g. from Separtis such as Isolute® Flash silica gel or Isolute® Flash NH 2 silica gel in combination with a Isolera® autopurifier (Biotage) and eluents such as gradients of e.g. hexane/ethyl acetate or DCM/methanol.
• Separtis such as Isolute® Flash silica gel or Isolute® Flash NH 2 silica gel in combination with a Isolera® autopurifier (Biotage) and eluents such as gradients of e.g. hexane/ethyl acetate or DCM/methanol.
• the compounds may be purified by preparative HPLC using for example a Waters autopurifier equipped with a diode array detector and/or on-line electrospray ionization mass spectrometer in combination with a suitable prepacked reverse phase column and eluents such as gradients of water and acetonitrile which may contain additives such as trifluoroacetic acid, formic acid or aqueous ammonia.
• a Waters autopurifier equipped with a diode array detector and/or on-line electrospray ionization mass spectrometer in combination with a suitable prepacked reverse phase column and eluents such as gradients of water and acetonitrile which may contain additives such as trifluoroacetic acid, formic acid or aqueous ammonia.
• purification methods as described above can provide those compounds of the present invention which possess a sufficiently basic or acidic functionality in the form of a salt, such as, in the case of a compound of the present invention which is sufficiently basic, a trifluoroacetate or formate salt for example, or, in the case of a compound of the present invention which is sufficiently acidic, an ammonium salt for example.
• a salt of this type can either be transformed into its free base or free acid form, respectively, by various methods known to the person skilled in the art, or be used as salts in subsequent biological assays. It is to be understood that the specific form (e.g. salt, free base etc) of a compound of the present invention as isolated as described herein is not necessarily the only form in which said compound can be applied to a biological assay in order to quantify the specific biological activity.
• the crystals were washed with cold methanol and dried in vacuo at 50° C. The crystallization was repeated twice with cold methanol to receive 2 further filter cakes and a combined yield of 6.87 g (19 mmol, 82.5%) of the analytically pure target compound.
• reaction mixture was cooled again with an ice bath and 0.059 ml of pyridine (0.727 mmol, 2.5 eq.) and 0.061 ml of trifluoromethanesulfonic anhydride (0.364 mmol, 1.25 eq.) were added and stirred for 3 hours. This procedure was repeated and stirred for further 24 hours.
• 1-16-2 SM 1-18-1 2-(bromo- methyl)-1,3- difluoro-5- propoxy- benzene
• 1-16-3 SM 1-18-2 2-(bromo- methyl)-1,3- difluoro-5-(2- methoxy- ethoxy) benzene
• 2-53-1 SM 1-6-1 2-[1-(4-ethoxy- 2-fluoro-6- methoxyben- zyl)-1H-indazol- 3-yl]-5- methoxy-N- (pyridin-4- yl)pyrimidin-4- amine
• ⁇ [ppm] 1.26 (t, 3H), 3.72 (s, 3H), 3.92-4.10 (m, 5H), 5.54 (s, 2H), 6.40 (s, 1H), 6.50 (dd, 1H), 7.13- 7.27 (m, 1H), 7.37- 7.49 (m, 1H), 7.79 (d, 1H), 8.16 (d, 2H), 8.31 (s, 1H), 8.35-8.47 (m, 3H), 9.38 (s, 1H).
• Step 1 2- ⁇ 1-[4-(1-ethoxyethenyl)-2,6-difluorobenzyl]-1H-indazol-3-yl ⁇ -5-methoxy-N-(pyridin-4-yl)pyrimidin-4-amine
• 9-2 SM 2-35-1 1-[3-( ⁇ 3-[5- methoxy-4- (pyridin-4- ylamino)pyrimidin- 2-yl]-1H-indazol-1- yl ⁇ methyl)phenyl]- 2-methylpropan-2- ol
• ⁇ [ppm] 0.94 (s, 6H), 1.18-1.22 (m, 2H), 4.02 (s, 3H), 4.24 (s, 1H), 5.70 (s, 2H), 7.03-7.25 (m, 5H), 7.38 (t, 1H), 7.74 (d, 1H), 8.12 (dd, 2H), 8.32- 8.46 (m, 4H), 9.40 - 9.45 (m, 1H).
• 10-2 SM 3-1 5- (difluoromethoxy)- N- (difluoromethyl)- 2-[1-(4-ethoxy- 2,6- difluorobenzyl)- 1H-indazol-3-yl]- N-(pyridin-4- yl)pyrimidin-4- amine
• Step 1 5- ⁇ [(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]methoxy ⁇ -2-[1-(2-fluorobenzyl)-1H-indazol-3-yl]-N-(pyridin-4-yl)pyrimidin-4-amine

Applications Claiming Priority (3)

Related Parent Applications (1)

Related Child Applications (1)

Publications (1)

Family

ID=46968229

Family Applications (3)

Family Applications After (2)

Country Status (38)

Cited By (6)

Families Citing this family (32)

Citations (1)

Family Cites Families (47)

• 2012
  • 2012-04-10 UA UAA201404803A patent/UA111754C2/uk unknown
  • 2012-10-04 DK DK12766997.6T patent/DK2763982T3/en active
  • 2012-10-04 HU HUE12766997A patent/HUE037154T2/hu unknown
  • 2012-10-04 ES ES12766997.6T patent/ES2665036T3/es active Active
  • 2012-10-04 CA CA2851037A patent/CA2851037A1/en not_active Abandoned
  • 2012-10-04 SG SG11201400616YA patent/SG11201400616YA/en unknown
  • 2012-10-04 WO PCT/EP2012/069562 patent/WO2013050438A1/en active Application Filing
  • 2012-10-04 CN CN201280059851.2A patent/CN103974948B/zh not_active Expired - Fee Related
  • 2012-10-04 LT LTEP12766997.6T patent/LT2763982T/lt unknown
  • 2012-10-04 US US14/350,160 patent/US20140249133A1/en active Granted
  • 2012-10-04 KR KR1020147011914A patent/KR102007056B1/ko active IP Right Grant
  • 2012-10-04 AU AU2012320582A patent/AU2012320582B2/en not_active Ceased
  • 2012-10-04 RS RS20180403A patent/RS57099B1/sr unknown
  • 2012-10-04 MX MX2014004122A patent/MX361279B/es active IP Right Grant
  • 2012-10-04 SI SI201231274T patent/SI2763982T1/en unknown
  • 2012-10-04 PL PL12766997T patent/PL2763982T3/pl unknown
  • 2012-10-04 EA EA201400412A patent/EA201400412A1/ru unknown
  • 2012-10-04 BR BR112014008045A patent/BR112014008045A2/pt not_active Application Discontinuation
  • 2012-10-04 JP JP2014533880A patent/JP6140170B2/ja not_active Expired - Fee Related
  • 2012-10-04 PE PE2014000471A patent/PE20141203A1/es active IP Right Grant
  • 2012-10-04 EP EP12766997.6A patent/EP2763982B1/en active Active
  • 2012-10-04 PT PT127669976T patent/PT2763982T/pt unknown
  • 2012-10-04 AP AP2014007533A patent/AP3847A/en active
  • 2012-10-04 NO NO12766997A patent/NO2763982T3/no unknown
  • 2012-10-05 UY UY0001034374A patent/UY34374A/es not_active Application Discontinuation
  • 2012-10-05 AR ARP120103719A patent/AR088449A1/es active Pending
  • 2012-10-05 TW TW101137035A patent/TWI588141B/zh not_active IP Right Cessation
• 2014
  • 2014-03-19 IL IL231591A patent/IL231591A/en active IP Right Grant
  • 2014-04-04 CR CR20140161A patent/CR20140161A/es unknown
  • 2014-04-04 EC ECSP14013284 patent/ECSP14013284A/es unknown
  • 2014-04-04 GT GT201400063A patent/GT201400063A/es unknown
  • 2014-04-04 TN TNP2014000138A patent/TN2014000138A1/en unknown
  • 2014-04-04 CU CUP2014000043A patent/CU20140043A7/es unknown
  • 2014-04-04 CO CO14073129A patent/CO6930363A2/es active IP Right Grant
  • 2014-04-04 DO DO2014000062A patent/DOP2014000062A/es unknown
• 2015
  • 2015-01-26 HK HK15100857.5A patent/HK1200449A1/xx not_active IP Right Cessation
• 2017
  • 2017-02-21 US US15/438,254 patent/US10266548B2/en not_active Expired - Fee Related
• 2018
  • 2018-04-04 HR HRP20180546TT patent/HRP20180546T1/hr unknown
  • 2018-04-10 CY CY20181100391T patent/CY1120318T1/el unknown
• 2019
  • 2019-03-21 US US16/360,811 patent/US10604532B2/en active Active

Patent Citations (1)

Non-Patent Citations (8)

Also Published As

Similar Documents

Legal Events