CN101012200A

CN101012200A - Process for preparing substituted pyrimidines and pyrimidine derivatives as inhibitors of protein kinases

Info

Publication number: CN101012200A
Application number: CN 200710085538
Authority: CN
Inventors: J-D·沙里耶; F·玛泽; D·凯; A·米勒
Original assignee: Vertex Pharmaceuticals Inc
Current assignee: Vertex Pharmaceuticals Inc
Priority date: 2002-06-20
Filing date: 2003-06-19
Publication date: 2007-08-08
Also published as: ZA200500414B; UA81420C2; ES2361335T3

Abstract

The present invention provides a facile process for the preparation of tri-and tetra-substituted pyrimidines. The process is useful for preparing inhibitors of protein kinases, especially Aurora kinase. These inhibitors are useful for treating or lessening the severity of Aurora-mediated diseases or conditions.

Description

Preparation is as the method for the pyrimidine and the pyrimidine derivatives of the replacement of kinases inhibitor

The application is to be June 19, application number in 2003 the dividing an application for the Chinese patent application of " preparation as the pyrimidine of the replacement of kinases inhibitor and the method for pyrimidine derivatives " that be 03818888.0 (PCT/US03/19266), denomination of invention the applying date.

The cross reference of related application

The application requires the right of priority of U.S. Provisional Patent Application of submitting on June 20th, 2,002 60/390,658 and the U.S. Provisional Patent Application of submitting on September 18th, 2,002 60/411,609, and their content is incorporated by reference here.

Technical field

The invention provides a kind of simple method for preparing the pyrimidine of replacement.Present method can be used to prepare the inhibitor of the inhibitor of protein kinase, particularly FLT-3 and Aurora family kinase, serine/threonine protein kitase.The invention still further relates to the inhibitor of FLT-3, Aurora-1, Aurora-2 and Aurora-3 protein kinase and their composition.

Background technology

Recent years, understand the research of having assisted the novel therapeutic medicine with the structure of target disease involved enzyme and other biomolecules greatly better.The important enzyme that one class has become the object of broad research is a protein kinase.

Protein kinase mediated intercellular signal transmission.They shift this effect of bringing into play by realizing the phosphinylidyne from nucleoside triphosphate to the protein receptor that participates in signalling channel.Extracellular stimulation with other causes the various cell responses that take place in cell by many kinases and passage.The example of this stimulation comprises ambient signal and chemical pressure signal (for example, osmotic pressure fluctuation, heat fluctuation, ultraviolet radiation, bacterial endotoxin and H ₂O ₂), cytokine (for example, il-1 (IL-1) and tumor necrosis factor alpha (TNF-α)), somatomedin (for example, granulocyte huge have a liking for cell-G CFS (GM-CSF) and fibroblast growth factor (FGF)).Extracellular stimulation may influence one or more and control the cell response relevant with regulation of Cell Cycle with activation, Muscle contraction, glucose metabolism, the albumen synthetic of cell growth, migration, differentiation, hormone secretion, transcription factor.

Numerous disease is relevant with the protein kinase mediated abnormal cells that process triggered reaction.These diseases comprise autoimmune disease, inflammation, osteopathy, metabolic disease, neurological disorder and nerve degeneration disease, cancer, cardiovascular diseases, allergy and asthma, Alzheimer and hormone relative disease.Therefore, carry out substantial effort in the pharmaceutical chemistry field and sought the kinases inhibitor that can be used as effective medicine.

The Aurora family of serine/threonine kinase is basic [Bischoff, J.R.﹠amp for cell proliferation; Plowman, G.D. (The Aurora/Ipllp kinase family:regulators of chromosome segregation and cytokinesis) Trends inCell Biology 9,454-459 (1999); Giet, R. and Prigent, C. (Aurora/Ipllp-related kinases, a new oncogenic family of mitoticserine-threonine kinases) Journal of Cell Science 112,3591-3601 (1999); Nigg, E.A. (mitotic kinases as regulators of celldivision and its checkpoints) Nat.Rev.Mol.Cell Biol.2,21-32 (2001); Adams, R.R, Carmena, M., and Earnshaw, W.C. (Chromosomalpassengers and the (aurora) ABCs of mitosis) Trends in CellBiology 11,49-54 (2001)].Therefore, the inhibitor of Aurora kinases family has the potentiality of the growth that stops all tumor types.

Three kinds of known Mammals family members, Aurora-A (" 1 "), B (" 2 ") and C (" 3 ") are the height homologous albumen of being responsible for chromosome segregation, mitotic spindle function and division of cytoplasm.The expression of Aurora in resting cell is low maybe can not to be detected, and occurs expressing and active peak in G2 and the mitotic division stage of cell cycle.In mammalian cell, infer that the matrix of Aurora comprises that histone H 3, the albumen that participates in the karyomit(e) condensation and CENP-A, myoglobulin I I regulate light chain, protein phosphatase 1, TPX2, cell fission needs them.

Since 1997 found, Mammals Aurora kinases family was taken place to connect nearly with tumour.The most convictive evidence of this respect is, the overexpression of Aurora-A can change rodentine inoblast (Bischoff, J.R., Deng people A homologue ofDrosophila aurora kinase is oncogenic and amplified in humancolorectal cancers.EMBO J.17,3052-3065 (1998)).There is the cell of this enzyme level of rising to contain a plurality of centrosomies and multipolar spindle, and becomes aneuploid soon.The kinase whose carcinogenic activity of Aurora is as relevant with the generation of this genetic instability.In fact, the amplification of aurora-A locus and the association (Miyoshi between the chromosome instability in mastadenoma and stomach knurl, have been observed, Y., Iwao, K., Egawa, C., and Noguchi, S.Association of centrosomal kinase STK15/BTAK mRNA expressionwith chromosomal instability in human breast cancers.Int. J.Cancer 92,370-37 3 (2001). (Sakakura, C. wait human Tum-5 or-amplifiedkinase BTAK is amplified and overexpressed in gastric cancerswith possible involvement in aneuploid formation.BritishJournal of Cancer 84,824-831 (2001)).Reported Aurora kinases overexpression in people's tumour of wide scope.At the colorectum (Bischoff that surpasses 50%, J.R., Deng people A homologue of Drosophila aurora kinase is oncogenic andamplified in human colorectal cancers.EMBO J.17,3052-3065 (1998)) (Takahashi, T., Deng people Centrosomal kinases, HsAIRk1 andHsAIRK3, are over expressed in primary colorectal cancers.Jpn.J.Cancer Res.91,1007-1014 (2000)), oophoroma (Gritsko, T.M. wait people Activation and overexpression of centrosome kinaseBTAK/Aurora-A in human ovarian cancer.Clinical Cancer Research9, people 1420-1426 (2003)), stomach knurl (Sakakura, C. wait human Tum-5 or-amplifiedkinase BTAK is amplified and overexpressed in gastric cancerswith possible involvement in aneuploid formation. BritishJournal of Cancer 84,824-831 (2001)) and 94% breast invasion catheter-like gland cancer (Tanaka, T., Deng people Centrosomal kinase AIK1 is over expressed ininvasive ductal carcinoma of the breast.Cancer Research.59,2041-2044 (1999)) rising that detects Aurora-A in is expressed.Also reported kidney, cervical cancer, neuroblastoma, melanoma, lymphoma, high-caliber Aurora-A (Bischoff in Vipoma and the prostate tumor clone, J.R., Deng people A homologue ofDrosophila aurora kinase is oncogenic and amplified in humancolorectal cancers.EMBO J.17,3052-3065 (1998) (Kimura, M., Matsuda, Y., Yoshioka, T., and Okano, Y.Cellcycle-dependentexpression and centrosomal localization of a third humanAurora/Ipll-related protein kinase, AIK3.Journal of BiologicalChemistry 274,7334-7340 (1999)) (human Tum-5 our amplifieckinaseSTK15/BTAK induces centrosome amplification such as Zhou, aneuploidyand transformation Nature Genetics 20:189-193 (1998)) (people Overexpression of oncogenic STK15/BTAK/Aurora-A kinase inhuman pancreatic cancer Clin Cancer Res.9 (3): 991-7 (2003) such as Li).In the human bladder cancer, find amplification/overexpression of Aurora-A, and relevant with invasive clinical behavior people Amplification/overexpression of a mitotic kinase gene in human bladder cancerJnatl Cancer Inst.94 (17): 1320-9 (2002) such as () the Sen S. of the amplification of Aurora-A and aneuploid.And, the patient with breast cancer that the amplification of aurora-A locus (20q 13) and joint (node) are negative is difficult to prediction (prognosis) relevant (Isola, J.J., Deng people Genetic aberrationsdetected by comparative genomic hybridization predict outcome innode-negative breast cancer.American Journal of Pathology 147,905-911 (1995)).Aurora-B is high expression level in the various human tumor cell line, and described clone comprises leukemia cell (people HumanAIM-1:cDNA cloning andreduced expression during endomitosis in megakaryocyte-lineagecells.Gene 244:1-7 such as Katayama).In initial colorectal cancer, the level of this enzyme increases (Katayama along with the Du Ke stage (Duke ' s stage), H. wait people Mitotic kinaseexpression and colorectal cancer progression.Journal of theNational Cancer Institute 91,1160-1162 (1999)).Aurora-C is general only to be found in sexual cell, it is with high per-cent overexpression (Kimura in (comprising adenocarcinoma of cervix and breast cancer cell) in initial colorectal cancer and kinds of tumor cells also, M., Matsuda, Y., Yoshioka, T., and Okano, Y.Cell cycle-dependentexpression and centrosomal localization of a third humanAurora/Ipll-related kinase, AIK3.Journal of BiologicalChemistry 274,7334-7340 (1999). (Takahashi, T., Deng people Centrosomal kinases, HsAIRkI and HsAIRK3, are over expressed inprimary colorectal cancers.Jpn. J.Cancer Res.91,1007-1014 (2000)).

Based on the kinase whose function of known Aurora, the activity that suppresses them can be interrupted the mitotic division that causes the cell cycle to stop.Therefore can slow down in vivo growth of tumor and induce degeneration of Aurora inhibitor.

In kinds of tumor cells system, observe all Aurora family members of elevated levels.The Aurora kinases is overexpression in many people's tumours, it is reported that this is relevant with chromosome instability in the mammary tumor (people 200192 such as Miyoshi, 370-373).

Aurora-2 is high expression level in the various human tumor cell line, and its level increases [Katayama along with the Du Ke stage (Duke ' s stage) of initial colorectal cancer, H. wait people (Mitotickinase expression and colorectal cancer progression) Journal ofthe National Cancer Institute 91,1160-1162 (1999)].Work aspect the chromosomal clean cut separation of Aurora-2 in control mitotic division process.The mistake adjusting of cell cycle can cause cell proliferation and other unusual.In the human colon carcinoma tissue, have been found that Aurora-2 albumen overexpression [people such as Bischoff, EMBO J., 17,3052-3065 (1998); People such as Schumacher, J Cell Biol., 143,1635-1646 (1998); People such as Kimura, J.Biol.Chem., 272,13766-13771 (1997)].Aurora-2 is overexpression in most of transformants.People such as Bischoff find, high-caliber Aurora-2 is arranged in 96% the clone that is derived from lung knurl, colon tumor, nephroncus, melanoma and mastadenoma, and (people EMBO such as Bischoff J.1998 17,3052-3065).Two extensive studies show, (people EMBO such as Bishoff J.1998 17 54% and 68%, 3052-3065) (people 2000 Jpn J Cancer Res.91 such as Takahashi, (people 1,999 59 such as Tanaka has the Aurora-2 of rising in 2041-2044) to colorectal carcinoma 1007-1014) and 94% breast invasion catheter-like gland cancer.

The expression of Aurora-1 in the clone that is derived from colon tumor, mastadenoma, lung knurl, melanoma, nephroncus, oophoroma, Vipoma, CNS, stomach tube knurl and leukemia knurl raise to some extent (people 1,998 58 such as Tatsuka, 4811-4816).

In several tumor cell lines, detected high-caliber Aurora-3, although it be only limited in the testis (testis) of healthy tissues (people 1,999 274 such as Kimura, 7334-7340).Also on the books, and overexpression Aurora-3 in the colorectal cancer of high per-cent (c.50%) (people 2000 Jpn J Cancer Res.91 such as Takahashi, 1007-1014).On the contrary, with low expression level, exception is the tissue that contains a high proportion of somatoblast to Aurora in most of healthy tissuess, and for example (people EMBO such as Bischoff J.1998 17,3052-3065) for thymus gland and testis.

Want further to understand Aurora kinases role in proliferative disease, referring to: Bischoff, J.R.﹠amp; Plowman, G.D. (The Aurora/Ipllp kinase family:regulators of chromosome segregation and cytokinesis) Trends inCell Biology 9,454-459 (1999); Giet, R. and Prigent, C. (Aurora/Ipllp-related kinases, a new oncogenic family of mitoticserine-threonine kinases) Journal of Cell Science 112,3591-3601 (1999); Nigg, E.A. (mitotic kinases as regulators of celldivision and its checkpoints) Nat.Rev.Mol.Cell Biol.2,21-32 (2001); Adams, R.R, Carmena, M., and Earnshaw, W.C. (Chromosomalpassengers and the (aurora) ABCs of mitosis) Trends in CellBiology 11,49-54 (2001); And Dutertre, S., Descamps, S. ， ﹠amp; Prigent, P. (On the role of aurora-A in centrosome function) Oncogene 21,6175-6183 (2002).

III receptor Tyrosylprotein kinase (the Flt3) [Scheijen that in the keeping of hematopoietic cell and non-hematopoietic cell, g and D, plays an important role, B, Griffin JD, Oncogene, 2002,21,3314-3333 and Reilly, JT, British Journal ofHaematology, 2002,116,744-757].FLT-3 regulates stem cell/early progenitor cell group's the growth [Lyman, S, Jacobsen, S, Blood, 1998,91,1101-1134] with sophisticated lymphocyte and medullary cell kept.FLT-3 contains inner kinases territory, and it can be activated by ligand-mediated receptor dimerizationization.After the activation, the automatic phosphorylation of acceptor and the phosphorylation of various plasmosins are induced in the kinases territory, and this helps to cause the transmission of the activation signals growing, break up and bring back to life.The downstream conditioning agent of some FLT-3 receptor signals comprises PLC γ, PI3-kinases, Grb-2, SHIP and Src associated kinase [Scheijen, B, Griffin JD, Oncogene, 2002,21,3314-3333].The FLT-3 kinases works in various hematopoiesis and malignant tumour non-hematopoiesis.Discovery causes the activatory of the part independence of FLT-3 to suddenly change in acute myelocytic leukemia (AML), acute lymphoblastic leukemia (ALL), mast cell disease and stomach stromal tumor (GIST).These sudden changes are included in the kinases territory or the single amino acids variation in (tandem duplication), the point mutation or the interior deletion of frame in acceptor membrane-proximal region territory are vertically duplicated in inside.Except activated mutant, the ligand dependent of the wild-type FLT-3 of overexpression (autocrine or paracrine) stimulation has encouraged malignant phenotype [Scheijen, B, Griffin JD, Oncogene, 2002,21,3314-3333].Also referring to Sawyer, C.I. (Finding the next Gleevec:FLT3targeted kinase inhibitor therapy for acute myeloid leukaemia) Cancer Cell.1,413-415 (2002).

Pyrimidine derivatives as three of kinase inhibitor-or four-replace known in the art.Typically, these pyrimidine derivatives are 2,4,6-or 2,4,5, and 6-replaces, and is as follows:

2,4,6-substituted pyrimidines 2,4,5, the pyrimidine that 6-replaces

The method of the pyrimidine derivatives that known preparation is such has many synthetic defectives, for example can not specifically reach high yield at 2-, 4-or 6-position introducing substituting group in the position.Referring to: M.Botta, Nucleosides Nucleotides, 13,8,1994,1769-78; M.Ban, Bioorg.Med.Chem., 6,7,1998,1057-68; Y.Fellahi, Eur.J.Med.Chem.Chim.Ther., 31,1,1996,77-82; T.J.Delia, J.Het.Chem., 35,2,1998,269-74; H.Uchel, Tetraheron Lett., 36,52,1995,9457-60; And Y.Nezu, Pestic.Sci., 47,2,1996,115-24.

Need easily to be used for to prepare on a large scale three-or four-synthetic method of the pyrimidine derivatives that replaces.Also need to adopt the method for minimum step, the easy raw material that obtains of use and simple reaction medium.Ideally, such method mass-producing and inexpensive easily when needed.Also need can not to produce the method for the intermediate mixture of the position isomerism that must separate (by for example chromatography method).Such branch defection reduces overall yield.

Should have a kind ofly can produce three-or four-synthetic method of the pyrimidine derivatives that replaces, it has above-mentioned advantage, thereby present obtainable method is improved.

Summary of the invention

The invention provides a kind of method of preparation I compound:

Wherein:

Among Q and the T each is independently selected from oxygen, sulphur or N (R);

Each R is independently selected from hydrogen or the optional C that replaces _1-6Aliphatic group, wherein:

Be attached on the same nitrogen-atoms two R randomly with this nitrogen-atoms form the monocyclic or first dicyclo of 8-10 of the optional 3-7 unit that replaces saturated, part is undersaturated or complete undersaturated ring, this ring also contains the individual heteroatoms that is independently selected from nitrogen, oxygen or sulphur of 0-3 except the bonded nitrogen-atoms;

R ^xBe U-R ⁵

R ⁵Be selected from halogen, NO ₂, CN, R or Ar;

Each U is independently selected from valence link or C _1-4Alkylidene chain, wherein:

Maximum 2 MU (methylene unit) randomly and independently are replaced by among the U :-O-,-S-,-SO-,-SO ₂-,-N (R) SO ₂-,-SO ₂N (R)-,-N (R)-,-C (O)-,-CO ₂-,-N (R) C (O)-,-N (R) C (O) O-,-N (R) CON (R)-,-N (R) SO ₂N (R)-,-N (R) N (R)-,-C (O) N (R)-,-OC (O) N (R)-,-C (R)=NN (R) or-C (R)=N-O-;

Each Ar is independently selected from the optional ring that replaces, this ring be selected from the monocyclic or first dicyclo of 8-10 of 3-7 unit saturated, part is undersaturated or the undersaturated 0-4 of containing heteroatomic ring fully, described heteroatoms is independently selected from nitrogen, oxygen or sulphur;

R ^yBe-N (R ¹) ₂,-OR ¹Or-SR ¹

Each R ¹Be independently selected from monocyclic, the first dicyclo of 8-10 or the 10-12 of R or 3-8 unit unit trinucleated saturated, part is undersaturated or the undersaturated 0-4 of containing heteroatomic ring fully, described heteroatoms is independently selected from nitrogen, oxygen or sulphur, wherein:

Each R ¹Randomly and independently be selected from R by maximum 4 ²Substituting group replace;

Each R ²Be independently selected from :-R ³,-OR ³,-SR ³,-CN ,-NO ₂, oxo, halogen ,-N (R ³) ₂,-C (O) R ³,-OC (O) R ³,-CO ₂R ³,-SO ₂R ³,-SO ₂N (R ³) ₂,-N (R ³) SO ₂R ³,-C (O) NR (R ³) ,-C (O) N (R ³) ₂,-OC (O) NR (R ³) ,-OC (O) N (R ³) ₂,-NR ³C (O) R ³,-NR ³C (O) N (R ³) ₂Or-NR ³CO ₂(R ³);

Each R ³Be independently selected from R or Ar;

R ^ZlBe selected from C _1-6Monocyclic, the first dicyclo of 8-10 or the 10-12 of aliphatic group or 3-8 unit unit trinucleated saturated, part is undersaturated or undersaturatedly fully contain 0-4 heteroatomic ring, described heteroatoms is independently selected from nitrogen, oxygen or sulphur, wherein:

R ^Z1Be independently selected from R by 0-4 ²The substituting group of group replaces;

R ^Z2Be C _1-6Aliphatic group or 3-8 unit are monocyclic, the first dicyclo of 8-10 saturated, part is undersaturated or undersaturatedly fully contain 0-4 heteroatomic ring, described heteroatoms is independently selected from nitrogen, oxygen or sulphur, wherein:

R ^Z2Be independently selected from oxo or U-R by 0-4 ⁵Substituting group replace;

Described method is included in the suitable medium formula II compound and formula R ^yThe step of-H compound combination:

R ^y-H

Wherein:

Described suitable medium comprises:

I) suitable solvent; With

Ii) randomly, suitable alkali; And

L ³It is suitable leavings group.

Detailed Description Of The Invention

The invention provides a kind of method of preparation I compound:

Wherein:

Among Q and the T each is independently selected from oxygen, sulphur or N (R);

R ^xBe U-R ⁵

R ⁵Be selected from halogen, NO ₂, CN, R or Ar;

R ^yBe-N (R ¹) ₂,-OR ¹Or-SR ¹

Each R ³Be independently selected from R or Ar;

R ^Z1Be selected from C _1-6Monocyclic, the first dicyclo of 8-10 or the 10-12 of aliphatic group or 3-8 unit unit trinucleated saturated, part is undersaturated or undersaturatedly fully contain 0-4 heteroatomic ring, described heteroatoms is independently selected from nitrogen, oxygen or sulphur, wherein:

R ^y-H

Wherein:

Described suitable medium comprises:

I) suitable solvent; With

Ii) randomly, suitable alkali; And

L ³It is suitable leavings group.

According to the another one embodiment, by in suitable medium with formula III compound and formula R ^Z1-Q-H compound makes up preparation formula II compound:

R ^z1-Q-H

Wherein:

Described suitable medium comprises:

I) suitable solvent; With

Ii) randomly, suitable alkali; And

L ²It is suitable leavings group.

According to the another one embodiment, by in suitable medium with formula IV compound and formula R ^Z2-T-H compound makes up and prepares the formula III compound:

R ^z2-T-H

Wherein:

Described suitable medium comprises:

I) suitable solvent; With

Ii) randomly, suitable alkali; And

L ¹It is suitable leavings group.

Combined solvent or the solvent mixture that helps later the reaction process between them of compound that suitable solvent is and will makes up.This suitable solvent can dissolve one or more reactive components, and perhaps replacedly, this suitable solvent helps the stirring of the suspension of one or more reactive components.The example of operable in the present invention suitable solvent is protonic solvent, halohydrocarbon, ether, aromatic hydrocarbon, polar or nonpolar aprotic solvent or other any mixture.These and other suitable like this solvent is well known in the art, for example, referring to: " AdvancedOrganic Chemistry ", Jerry March, 4 ^ThEdition, John Wiley and Sons, N.Y. (1992).

Suitable solvent is C preferably _1-7The alkyl alcohol of straight or branched, ether or polar or nonpolar aprotic solvent.

In order to carry out formula II compound and formula R ^yReaction between the-H compound, preferred suitable solvent is to be selected from: ethanol, Virahol, the trimethyl carbinol, propyl carbinol or tetrahydrofuran (THF).

In order to carry out formula III compound and formula R ^Z1Reaction between the-Q-H compound, preferred suitable solvent is to be selected from: ethanol, Virahol, the trimethyl carbinol, propyl carbinol, N, dinethylformamide, dimethyl sulfoxide (DMSO) or tetrahydrofuran (THF).

In order to carry out formula IV compound and formula R ^Z2Reaction between the-T-H compound, preferred suitable solvent is to be selected from: N, dinethylformamide, dimethyl sulfoxide (DMSO) or tetrahydrofuran (THF).

According to other embodiments, suitable solvent is R ^y-H.Like this, in this embodiment, reagent R ^y-H partly as with the suitable solvent of formula II compound combination, also partly as with the reagent of formula II compound reaction production I compound.

According to the another one embodiment, suitable solvent is R ^Z1-Q-H.Like this, in this embodiment, reagent R ^Z1-Q-H partly as with the suitable solvent of formula III compound combination, also partly as with the reagent of formula III compound reaction production II compound.

According to the another one embodiment, suitable solvent is R ^Z2-T-H.Like this, in this embodiment, reagent R ^Z2-T-H partly as with the suitable solvent of formula IV compound combination, also partly as generating the reagent of formula III compound with the reaction of formula IV compound.

Suitable alkali is can be as proton acceptor's chemical substance.The example comprises organic amine, alkaline earth metal carbonate, alkaline earth metal hydride and alkaline earth metal hydroxides.These and other suitable like this alkali is well known in the art, for example, referring to: " Advanced OrganicChemistry ", Jerry March, 4 ^ThEdition, pp.248-253, John Wiley andSons, N.Y. (1992).Preferred suitable alkali comprises trialkylamine, yellow soda ash, salt of wormwood, sodium hydride, potassium hydride KH, sodium hydroxide or potassium hydroxide.More preferably, suitable alkali is diisopropyl ethyl amine or triethylamine.

Suitable leavings group is the chemical group that can easily be replaced by the chemical group that ideal is introduced.Like this, according to the chemical group R that can be introduced into ^yR among the-H ^y, R ^Z1R among the-Q-H ^Z1-Q or R ^Z2R among the-T-H ^Z2The performance that-T easily replaces can be selected specific suitable leavings group.Suitable leavings group is well known in the art, for example, referring to: " Advanced OrganicChemistry ", Jerry March, 4 ^ThEdition, pp.351-357, John Wiley andSons, N.Y. (1992).Such leavings group includes but not limited to halogen, alkoxyl group, alkylsulfonyl oxygen base, the optional alkyl sulphonyl that replaces, the optional alkenyl alkylsulfonyl that replaces, optional aryl sulfonyl and the diazo that replaces.The example of suitable leavings group comprises chlorine, iodine, bromine, fluorine, methane sulfonyl (methylsulfonyl), tosyl group, trifluoromethanesulfonic acid base, nitro-phenyl sulfonyl (p-nitrophenyl alkylsulfonyl) and bromo-phenyl sulfonyl (p-bromobenzenesulfonyl).

For example, in the method for preparation I compound, L ³The R that is introduced into ^yR among the-H ^yReplace.Like this, if R ^y-H is for example piperazine, L so ³Can by in the piperazine-leavings group that the NH-group easily replaces.

Preferred L ³Leavings group is to be selected from halogen, the optional aryl sulfonyl that replaces or the optional alkyl sulphonyl that replaces.More preferably, L ³Be chlorine, iodine, methane sulfonyl.Most preferably, L ³Be chlorine.

For example, in the method for preparation formula II compound, L ²The R that is introduced into ^Z1R among the-Q-H ^Z1-Q replaces.Like this, if R ^Z1-Q-H is for example 3-amino-pyrazol, L so ²It is the leavings group that can easily be replaced by the 3-amino-pyrazol.

Preferred L ²Leavings group is to be selected from halogen, the optional aryl sulfonyl that replaces or the optional alkyl sulphonyl that replaces.More preferably, L ²Be chlorine, iodine or fluorine.Most preferably, L ²Be chlorine.

For example, in the method for preparing the formula III compound, L ¹The R that is introduced into ^Z2R among the-T-H ^Z2-T replaces.Like this, if R ^Z2-T is for example optional artyl sulfo that replaces, L so ¹It is the leavings group that the sulfenyl in the artyl sulfo that can be optionally substituted easily replaces.

Preferred L ¹Leavings group is to be selected from halogen, the optional aryl sulfonyl that replaces or the optional alkyl sulphonyl that replaces.More preferably, L ¹Be chlorine, iodine or methane sulfonyl.Most preferably, L ¹It is methane sulfonyl.

According to a replacement embodiment, suitable leavings group can original position produce in reaction medium.For example, the L in the formula II compound ³Can be in position from the precursor generation of formula II compound, wherein said precursor contains can easily replace with L in position ³Group.In the special explanation of this replacement, the precursor of described formula II compound contains and replaces with L in position ³The group of (for example iodo) (for example, chloro or hydroxyl).The source of iodo can be a sodium iodide for example.Therefore, L ²And L ¹Also can form in position by similar mode.It is this that to produce suitable leavings group in position be well known in the art, for example, referring to: " Advanced Organic Chemistry, " Jerry March, pp.430-431,4 ^ThEd., John Wiley and Sons, N.Y. (1992).

Replace embodiment, R according to another one ^yThe R of-H ^y, R ^Z1The R of-Q-H ^Z1-Q or R ^Z2The R of-T-H ^Z2Any one negatively charged ion among the-T just forms before can be in joining reaction medium.Described anionic preparation is that those skilled in the art is known.For example, when T is oxygen, by handling R with alkali (for example sodium hydride) ^Z2-T-H can easily generate R ^Z2The negatively charged ion of-T-H.This oxygen anion can generate the formula III compound with the combination of formula IV compound then.

According to the another one embodiment, reaction described herein is to carry out under the temperature of the reflux temperature of being less than or equal to reaction medium.According to the another one embodiment, the temperature of described reaction medium is lower than the boiling point of described suitable solvent, perhaps is in by the resulting temperature of described suitable solvent that refluxes in described reaction medium.In the another one embodiment, the temperature of described reaction medium is about 0 ℃～about 190 ℃.In the another one embodiment, the temperature of described reaction medium is about 40 ℃～about 120 ℃.In the another one embodiment, the temperature of described reaction medium is about 7 ℃～about 115 ℃.

As used herein, unless otherwise indicated will adopt following definition.

Term " Aurora " is meant any isomer of the protein kinase of Aurora family, comprises Aurora-1, Aurora-2 and Aurora-3.Term " Aurora " also refers to the isomer of the protein kinase of Aurora family, and known is Aurora-A, Aurora-B and Aurora-C.

Term " optional replacement " can exchange use with term " replacement or unsubstituted ".Except as otherwise noted, the optional group that replaces can have substituting group on any commutable position of this group, and each replacement is separate.

Be meant C straight chain or side chain as term used herein " aliphatic series " or " aliphatic group " ₁-C ₈Hydrocarbon chain, this hydrocarbon chain are saturated fully or contain one or more unsaturated units, or monocyclic C ₃-C ₈The C of hydrocarbon or dicyclo ₈-C ₁₂Hydrocarbon, this hydrocarbon is saturated fully or contains one or more unsaturated units, but be not aromatic (being also referred to as " carbocyclic ring " or " cycloalkyl " here), it has single and other molecule bonded site, and any one ring in the wherein said bicyclic system all is a 3-7 unit.For example, suitable aliphatic group includes but not limited to linear or ramose alkyl, alkenyl, alkynyl and their heterocomplex, for example (cycloalkyl) alkyl, (cycloalkenyl group) alkyl or (cycloalkyl) thiazolinyl.

That use separately or as more the term of the part of macoradical " alkyl ", " alkoxyl group ", " hydroxyalkyl ", " alkoxyalkyl " and " alkoxy carbonyl " comprise straight chain and the side chain that contains 1～12 carbon atom.That use separately or as more the term of the part of macoradical " alkenyl " and " alkynyl " should comprise straight chain and the side chain that contains 2～12 carbon atoms.

Term " heteroatoms " is meant nitrogen, oxygen or sulphur, and comprises the quaternized form of any oxidised form and the basic nitrogen of nitrogen and sulphur.Term " nitrogen " also comprises commutable nitrogen in the heterocycle.As an example, saturated or the undersaturated 0-3 of containing of part be selected from the heteroatomic ring of oxygen, sulphur or nitrogen, nitrogen can be N (resembling 3, in the 4-dihydro-2 h-pyrrole base), NH (resembling in pyrrolidyl) or NR ⁺(resembling in the pyrrolidyl that N-replaces).

Term " aryl " or " aromatic nucleus " are meant that monocyclic, dicyclo or trinucleated contains the altogether loop systems of 5～14 ring carbon atoms, and wherein at least one ring is an aromatic nucleus, and wherein each ring in the system all contains 3～7 annular atomses.Term " aryl " can use interchangeably with term " aromatic nucleus ".The example comprises phenyl, indanyl, 1-naphthyl, 2-naphthyl, 1-anthryl, 2-anthryl and dicyclo [2.2.2] oct-3-yl.

In the different preferred embodiments of formula I compound, the ring size of preferred aromatic nucleus is as described below.

That use separately or as " aralkyl ", " aralkoxy " or " aryloxy alkyl " etc. more the term of the part of macoradical " aryl " be meant that monocyclic, dicyclo or trinucleated contains the loop systems that amounts to 5～14 annular atomses, wherein at least one ring in the system is an aromatic nucleus, and wherein the ring of each in the system all contains 3～7 annular atomses.Term " aryl " can use interchangeably with term " aromatic nucleus ".Term " aryl " also refers to the heteroaromatic ring system that defines hereinafter.

Term used herein " heterocycle ", " heterocyclic radical " or " heterocyclic " are meant that monocyclic, dicyclo or the trinucleated of non-fragrance contains the loop systems of 5～14 annular atomses, one of them or several annular atoms are heteroatomss, and wherein the ring of each in the system all contains 3～7 annular atomses.

That use separately or as " heteroaralkyl " or " heteroaryl alkoxyl group " wait more that the term of the part of macoradical " heteroaryl " is meant that monocyclic, dicyclo or trinucleated contains the loop systems that amounts to 5～14 annular atomses, wherein at least one ring in the system is an aromatic nucleus, at least one ring in the system contains one or more heteroatomss, and wherein the ring of each in the system all contains 3～7 annular atomses.Term " heteroaryl " can use interchangeably with term " hetero-aromatic ring " or term " assorted virtue ".

Aryl (comprising aralkyl, aralkoxy, aryloxy alkyl etc.) or heteroaryl (comprising heteroaralkyl and heteroaryl alkoxyl group etc.) can contain one or more substituting groups.Suitable substituents on the unsaturated carbon atom of aryl, heteroaryl, aralkyl or heteroaralkyl is to be selected from: halogen ,-R ^o,-OR ^o,-SR ^o, 1,2-methylene radical-dioxy, ethylene dioxy, with R ^oThe optional phenyl (Ph) that replaces, with R ^oOptional replace-O (Ph), with R ^oOptional replacement-CH ₂(Ph), with R ^oOptional replacement-CH ₂CH ₂(Ph) ,-NO ₂,-CN ,-N (R ^o) ₂,-NR ^oC (O) R ^o,-NR ^oC (O) N (R ^o) ₂,-NR ^oCO ₂R ^o,-NR ^oNR ^oC (O) R ^o,-NR ^oNR ^oC (O) N (R ^o) ₂,-NR ^oNR ^oCO ₂R ^o,-C (O) C (O) R ^o,-C (O) CH ₂C (O) R ^o,-CO ₂R ^o,-C (O) R ^o,-C (O) N (R ^o) ₂,-OC (O) N (R ^o) ₂,-S (O) ₂R ^o,-SO ₂N (R ^o) ₂,-S (O) R ^o,-NR ^oSO ₂N (R ^o) ₂,-NR ^oSO ₂R ^o,-C (=S) N (R ^o) ₂,-C (=NH)-N (R ^o) ₂Or-(CH ₂) _yNHC (O) R ^o, each R wherein ^oBe independently selected from oxo, halogen, the optional C that replaces _1-6Fat, undersaturated 5-6 unit's heteroaryl or heterocyclic ring, phenyl ,-O (Ph) or-CH ₂(Ph).R ^oOptional substituting group on the aliphatic group is selected from NH ₂, NH (C _1-4Aliphatic group), N (C _1-4Aliphatic group) 2, halogen, C _1-4Aliphatic group, OH, O (C _1-4Aliphatic group), NO ₂, CN, CO ₂H, CO ₂(C _1-4Aliphatic group), O (halo C _1-4Aliphatic group) or halo C _1-4Aliphatic group.

The heterocycle of aliphatic group or non-aromatic can contain one or more substituting groups.Suitable substituents on the heterocyclic saturated carbon of aliphatic group or non-aromatic be selected from the above those and following these the :=O that list for the unsaturated carbon of aryl or heteroaryl ,=S ,=NNHR ^*,=NN (R ^*) ₂,=NNHC (O) R ^*,=NNHCO ₂(alkyl) ,=NNHSO ₂(alkyl) or=NR ^*, each R wherein ^*Be independently selected from hydrogen or the optional C that replaces _1-6Aliphatic group.R ^*Optional substituting group on the aliphatic group is selected from: NH ₂, NH (C _1-4Aliphatic group), N (C _1-4Aliphatic group) ₂, halogen, C _1-4Aliphatic group, OH, O (C _1-4Aliphatic group), NO ₂, CN, CO ₂H, CO ₂(C _1-4Aliphatic group), O (halo C _1-4Aliphatic group) or halo (C _1-4Aliphatic group).

Optional substituting group on the non-aromatic heterocyclic nitrogen is selected from R ⁺,-N (R ⁺) ₂,-C (O) R ⁺,-CO ₂R ⁺,-C (O) C (O) R ⁺,-C (O) CH ₂C (O) R ⁺,-SO ₂R ⁺,-SO ₂N (R ⁺) ₂,-C (=S) N (R ⁺) ₂,-C (=NH)-N (R ⁺) ₂Or-NR ⁺SO ₂R ⁺R wherein ⁺Be hydrogen, the optional C that replaces _1-6Aliphatic group, the optional phenyl that replaces, optional replace-O (Ph), optional replace-CH ₂(Ph), optional replace-CH ₂CH ₂(Ph) or unsubstituted 5-6 unit heteroaryl or heterocycle.Aliphatic group or R ⁺Optional substituting group on the phenyl ring is selected from NH ₂, NH (C _1-4Aliphatic group), N (C _1-4Aliphatic group) ₂, halogen, C _1-4Aliphatic group, OH, O (C _1-4Aliphatic group), NO ₂, CN, CO ₂H, CO ₂(C _1-4Aliphatic group), O (halo C _1-4Aliphatic group) or halo (C _1-4Aliphatic group).

Term " alkylidene chain " is meant straight chain or ramose carbochain, and it can be saturated fully or have one or more unsaturated units, and have two and other molecule bonded site.

The combination of substituting group or variable only is only permission when this combination can produce stable or chemically feasible compound.Stable or chemically feasible compound is to be in 40 ℃ or lower temperature, not have the compound that still do not change basically at least one week in moisture or other the chemical reaction condition.

Those skilled in the art can understand that there is tautomer in some compound of the present invention, and all such tautomers of compound all within the scope of the invention.

Unless stated otherwise, the structure of mentioning here also is intended to comprise all stereochemical forms of this structure; That is, the R of each asymmetric center and S configuration.Therefore, the single three-dimensional chemical isomer of The compounds of this invention and enantiomer and non-enantiomer mixture are all within the scope of the invention.Unless stated otherwise, the structure of mentioning here is intended to also comprise that difference only is to exist the compound of the atom of enrichment on one or more isotropic substances.For example, except just hydrogen being replaced with deuterium or tritium or carbon being replaced with ¹³C-or ¹⁴Outside the carbon of C-enrichment, the compound with this structure also within the scope of the invention.Such compound can be used as, for example, and experimental tool in the Bioexperiment or probe.

According to the another one embodiment, the Q of formula I is NH, oxygen or sulphur.

According to an embodiment preferred, the Q of formula I is NR.More preferably, the Q of formula I is NH.

According to the another one embodiment preferred, the T of formula I is oxygen or sulphur.More preferably, the T of formula I is a sulphur.

According to the another one embodiment, the T of formula I is an oxygen, and R ^Z2The negatively charged ion of-T-H with formula IV compound combinations produce formula III compound before just form.

According to the another one embodiment, the R of formula I ^xBe U-R ⁵, wherein U be valence link ,-O-or-NR-, and R5 is R or Ar.

According to the another one embodiment preferred, the R of formula I ^xBe be selected from R, Ar or-N (R) ₂More preferably, the R of formula I ^xBe hydrogen.

According to the another one embodiment preferred, the R of formula I ^yBe to be selected from-OR ¹Or-N (R ¹) ₂

According to the another one embodiment preferred, the R of formula I ^yBe to be selected from-N (R ¹) ₂, each R wherein ¹Be independently selected from the monocyclic or first dicyclo of 8-10 of R or 3-7 unit saturated, part is undersaturated or the undersaturated 0-4 of containing heteroatomic ring fully, described heteroatoms is independently selected from nitrogen, oxygen or sulphur.Preferred substituted R ¹Be selected from :-OR ³,-SR ³,-CN ,-NO ₂, oxo, halogen ,-N (R ³) ₂,-C (O) R ³Or 3-6 unit contain 0-2 heteroatomic aromatic nucleus or non-aromatic ring, described heteroatoms is independently selected from nitrogen, oxygen or sulphur.Preferred R ¹On substituting group be 5-6 unit contain 1-2 heteroatomic non-aromatic ring, described heteroatoms is independently selected from nitrogen, oxygen or sulphur.Most preferred R ¹C _1-4Substituting group on the aliphatic group is NH (CH ₃), NH ₂, OH, OCH ₃, morpholinyl, piperidyl, piperazinyl, pyrrolidyl and thio-morpholinyl.

According to the another one embodiment preferred, the R of formula I ^yBe to be selected from-N (R ¹) ₂, each R wherein ¹All be R, such two R groups form the optional 4-7 unit non-aromatic ring that replaces together, and it contains 2 other heteroatomss that are independently selected from nitrogen, oxygen or sulphur at the most.Preferred substituted on the described ring is selected from: R ³,-OR ³,-SR ³,-CN ,-NO ₂, oxo, halogen ,-N (R ³) ₂,-C (O) R ³,-CO ₂R ³,-SO ₂R ³Or 3-6 unit contain 0-2 heteroatomic aromatic nucleus or non-aromatic ring, described heteroatoms is independently selected from nitrogen, oxygen or sulphur.More preferred substituents on the described ring is selected from: the optional C that replaces _1-4Aliphatic group, NH ₂, NH (C _1-4Aliphatic group), N (C _1-4Aliphatic group) ₂, optional phenyl, the CO that replaces ₂(C _1-4Aliphatic group) or SO ₂(C _1-4Aliphatic group).Most preferred substituting group is selected from methyl, ethyl, methylsulfonyl, (CH on the described ring ₂) ₂SO ₂CH ₃, cyclopropyl, CH ₂Cyclopropyl, (CH ₂) ₂OH, CO ₂The tertiary butyl, CH ₂Phenyl, phenyl, NH ₂, NH (CH ₃), N (CH ₃) ₂, (CH ₂) ₂NH ₂, (CH ₂) ₂Morpholine-4-base, (CH ₂) ₂N (CH ₃) ₂, sec.-propyl, propyl group, the tertiary butyl, (CH ₂) ₂CN or (CH ₂) ₂C (O) morpholine-4-base.

Most preferably, the R of formula I ^yBe tetramethyleneimine-1-base, piperidines-1-base, morpholine-4-base, thiomorpholine-4-base, piperazine-1-base, diazacyclo heptyl or the different isoquinolyl of tetrahydrochysene, wherein each ring is randomly replaced by one or more substituting groups that are independently selected from following radicals: methyl, ethyl, methylsulfonyl, (CH ₂) ₂SO ₂CH ₃, cyclopropyl, CH ₂Cyclopropyl, (CH ₂) ₂OH, CO ₂The tertiary butyl, CH ₂Phenyl, phenyl, NH ₂, NH (CH ₃), N (CH ₃) ₂, (CH ₂) ₂NH ₂, (CH ₂) ₂Morpholine-4-base, (CH ₂) ₂N (CH ₃) ₂, sec.-propyl, propyl group, the tertiary butyl, (CH ₂) ₂CN or (CH ₂) ₂C (O) morpholine-4-base.

According to the another one embodiment, the R of formula I ^Z1Be the monocyclic or first dicyclo of 8-10 of 3-7 unit saturated, part is undersaturated or the undersaturated 0-4 of containing heteroatomic ring fully, described heteroatoms is independently selected from nitrogen, oxygen or sulphur, and wherein said ring is replaced by 3 substituting groups that are selected from following radicals at the most randomly and independently :-R ³,-OR ³,-SR ³,-CN ,-NO ₂, oxo, halogen ,-N (R ³) ₂,-C (O) R ³,-OC (O) R ³,-CO ₂R ³,-SO ₂R ³,-SO ₂N (R ³) ₂,-N (R ³) SO ₂R ³,-C (O) NR (R ³) ,-C (O) N (R ³) ₂,-OC (O) NR (R ³) ,-OC (O) N (R ³) ₂,-NR ³C (O) R ³,-NR ³C (O) N (R ³) ₂Or-NR ³CO ₂R ³

According to the another one embodiment, the R of formula I ^Z1Be the monocyclic or first dicyclo of 8-10 of 5-6 unit saturated, part is undersaturated or the undersaturated 1-4 of containing heteroatomic ring fully, described heteroatoms is independently selected from nitrogen, oxygen or sulphur, and wherein said ring is replaced by 3 substituting groups that are selected from following radicals at the most randomly and independently :-R ³,-OR ³,-SR ³,-CN ,-NO ₂, oxo, halogen ,-N (R ³) ₂,-C (O) R ³,-OC (O) R ³,-CO ₂R ³,-SO ₂R ³,-SO ₂N (R ³) ₂,-N (R ³) SO ₂R ³,-C (O) NR (R ³) ,-C (O) N (R ³) ₂,-OC (O) NR (R ³) ,-OC (O) N (R ³) ₂,-NR ³C (O) R ³,-NR ³C (O) N (R ³) ₂Or-NR ³CO ₂R ³

According to a preferred embodiment, the R of formula I ^Z1Be the complete undersaturated 1-3 of containing a heteroatomic ring of 5 or 6 yuan, described heteroatoms is independently selected from nitrogen, oxygen or sulphur, and wherein said ring is replaced by 3 substituting groups that are selected from following radicals at the most randomly and independently :-R ³,-OR ³,-SR ³,-CN ,-NO ₂, oxo, halogen ,-N (R ³) ₂,-C (O) R ³,-OC (O) R ³,-CO ₂R ³,-SO ₂R ³,-SO ₂N (R ³) ₂,-N (R ³) SO ₂R ³,-C (O) NR (R ³) ,-C (O) N (R ³) ₂,-OC (O) NR (R ³) ,-OC (O) N (R ³) ₂,-NR ³C (O) R ³,-NR ³C (O) N (R ³) ₂Or-NR ³CO ₂R ³

The R of preferred formula I ^Z1Ring is the optional ring that replaces, and it is selected from pyrazoles or the following 5-6 unit ring any one:

Most preferably, the R of formula I ^Z1Ring is to contain maximum 3 substituent pyrazoles rings defined above.

According to another embodiment preferred, the R of formula I ^Z1Contain 2 substituting groups at the most, wherein said substituting group as mentioned above.More preferably, the R of formula I ^Z1Contain 1 substituting group, wherein said substituting group as mentioned above.

The R of preferred formula I ^Z1Substituting group on the group is-N (R ³) ₂,-OR ³, Ar or the optional C that replaces ₁-C ₄Aliphatic group, wherein Ar be the optional 5-6 unit that replaces saturated, part is undersaturated or the undersaturated 0-4 of containing heteroatomic ring fully, described heteroatoms is independently selected from nitrogen, oxygen or sulphur.The R of preferred formula I ^Z1Substituting group on the group is C ₁-C ₄Aliphatic group.The R of most preferred formula I ^Z1Substituting group on the group is to be selected from: methyl, ethyl, propyl group, sec.-propyl, the tertiary butyl, cyclopropyl or phenyl.

According to another embodiment, the R of formula I ^Z1By 0-4 R ²The C that group replaces ₁- ₆Aliphatic group.Preferably, R ^Z1By 0-3 R ²Group replaces, wherein each R ²Be independently selected from R ³, oxo, halogen, N (R ³) ₂, CN or CO ₂R ³

According to an embodiment preferred, the R of formula I ^Z2Be the monocyclic or first dicyclo of 8-10 of 5-6 unit saturated, part is undersaturated or the undersaturated 0-4 of containing heteroatomic ring fully, described heteroatoms is independently selected from nitrogen, oxygen or sulphur, and wherein said ring quilt 3 substituting groups that are independently selected from following radicals at the most randomly replaces :-R ³,-OR ³,-SR ³,-CN ,-NO ₂, oxo, halogen ,-N (R ³) ₂,-C (O) R ³,-OC (O) R ³,-CO ₂R ³,-SO ₂R ³,-SO ₂N (R ³) ₂,-N (R ³) SO ₂R ³,-C (O) NR (R ³) ,-C (O) N (R ³) ₂,-OC (O) NR (R ³) ,-OC (O) N (R ³) ₂,-NR ³C (O) R ₃,-NR ³C (O) N (R ³) ₂Or-NR ³CO ₂R ³

More preferably, the R of formula I ^Z2Be selected from the optional ring that replaces, this ring be selected from the monocyclic or first dicyclo of 9-10 of 5-6 unit saturated, part is undersaturated or the undersaturated 0-4 of containing heteroatomic ring fully, described heteroatoms is independently selected from nitrogen, oxygen or sulphur; Wherein said ring is randomly by 3 substituting groups replacements that are independently selected from above-mentioned group at the most.Most preferably, the R of formula I ^Z2Be selected from phenyl, imidazolyl, pyrazolyl, pyridyl, pyridazinyl, pyrazinyl, naphthyl, tetralyl, benzimidazolyl-, benzothiazolyl, quinolyl, quinazolyl, benzo two pyranyls, isobenzofuran, indanyl, indyl, indoline, indazolyl or isoquinolyl, the R of its Chinese style I ^Z2Group quilt 3 above-mentioned substituting groups at the most randomly and independently replaces.

When existing, the R of preferred formula I ^Z2Substituting group is independently selected from: halogen ,-CN ,-NO ₂,-C (O) R ³,-CO ₂R ³,-C (O) NR (R ³) ,-NR ³C (O) R ³,-N (R ³) ₂,-N (R ³) SO ₂R ³,-NR ³C (O) N (R ³) ₂Or-NR ³CO ₂R ³The R of preferred formula I ^Z2On substituting group be independently selected from :-Cl ,-Br ,-F ,-CN ,-CF ₃,-COOH ,-CONHMe ,-CONHEt ,-NH ₂,-NHAc ,-NHSO ₂Me ,-NHSO ₂Et ,-NHSO ₂(n-propyl) ,-NHSO ₂(sec.-propyl) ,-NHCOEt ,-NHCOCH ₂NHCH ₃,-NHCOCH ₂N (CO ₂T-Bu) CH ₃,-NHCOCH ₂N (CH ₃) ₂,-NHCOCH ₂CH ₂N (CH ₃) ₂,-NHCOCH ₂CH ₂CH ₂N (CH ₃) ₂,-NHCO (cyclopropyl) ,-NHCO (sec.-propyl) ,-NHCO (isobutyl-) ,-NHCOCH ₂(morpholine-4-yl) ,-NHCOCH ₂CH ₂(morpholine-4-yl) ,-NHCOCH ₂CH ₂CH ₂(morpholine-4-yl) ,-NHCO ₂(tertiary butyl) ,-NH (cyclohexyl) ,-NHMe ,-NMe ₂,-OH ,-OMe, methyl, ethyl, cyclopropyl, sec.-propyl or the tertiary butyl.

According to the another one embodiment preferred, the R of formula I ^Z2Contain 2 substituting groups at the most, wherein said substituting group as mentioned above.More preferably, the R of formula I ^Z2Contain 1 substituting group, wherein said substituting group as mentioned above.Most preferably, the R of formula I ^Z2Containing 1 is selected from-NR ³C (O) R ³Substituting group, each R wherein ³Be independently selected from R or Ar, and wherein R is hydrogen or the optional C that replaces _1-4Aliphatic group.

According to the another one embodiment, the R of formula I ^Z2By 0-3 C that is independently selected from the substituting group replacement of following radicals _1-6Aliphatic group: halogen, oxo ,-CN ,-NO ₂,-C (O) R ³,-CO ₂R ³,-C (O) NR (R ³) ,-NR ³C (O) R ³,-N (R ³) ₂,-N (R ³) SO ₂R ³,-NR ³C (O) N (R ³) ₂Or-NR ³CO ₂R ³More preferably, the R of formula I ^Z2By 0-3 C that is independently selected from the substituting group replacement of following radicals _1-4Aliphatic group: halogen ,-CN ,-NO ₂,-C (O) R ³,-CO ₂R ³,-N (R ³) ₂Or-NR ³CO ₂R ³

R among the formula II ^x, T, Q, R ^Z1And R ^Z2Preferred embodiment the same with explanation in formula I to these groups.

R ^yR among the-H ^yThe preferred embodiment of group with in formula I to R ^yExplanation the same.

R in the formula III ^x, L ³, T and R ^Z2Preferred embodiment the same with explanation in formula I to these groups.

R ^Z1Q among the-Q-H and R ^Z1The preferred embodiment of group is the same with the explanation to these groups in formula I.

R among the formula IV ^x, L ³, L ²The same with the preferred embodiment of Q with explanation in formula I to these groups.

R ^Z2T among the-T-H and R ^Z2Preferred embodiment the same with explanation in formula I to these groups.

Preferably, the R in the method for the present invention ^xIt is suitable leavings group group in addition.

The preferred formula I compound of preparing by method of the present invention have general formula I ':

Or its pharmaceutically acceptable derivates or salt, wherein R ¹And R ³Definition as above.

The R of preferred formula I ' ¹Group is independently selected from R, and wherein R is hydrogen or the optional C that replaces _1-4Aliphatic group.The R of formula I ' ¹The C of group _1-4Substituting group on the aliphatic group is selected from :-OR ³,-SR ³,-CN ,-NO ₂, oxo, halogen ,-N (R ³) ₂,-C (O) R ³Or 3-6 unit contain 0-2 heteroatomic aromatic nucleus or non-aromatic ring, described heteroatoms is independently selected from nitrogen, oxygen or sulphur.The R of preferred formula I ' ¹The C of group _1-4Substituting group on the aliphatic group is 1-2 the heteroatomic non-aromatic ring that contain of 5-6 unit, and described heteroatoms is independently selected from nitrogen, oxygen or sulphur.The R of most preferred formula I ' ¹The C of group _1-4Substituting group on the aliphatic group is NH (CH ₃), NH ₂, OH, OCH ₃, morpholinyl, piperidyl, piperazinyl, pyrrolidyl and thio-morpholinyl.

According to another embodiment preferred, each R of formula I ' ¹All be R, such two R form the optional 4-7 unit non-aromatic ring that replaces together, and this ring also contains 2 other heteroatomss that are independently selected from nitrogen, oxygen or sulphur at the most.Preferred substituted on the described ring is selected from :-R ³,-OR ³,-SR ³,-CN ,-NO ₂, oxo, halogen ,-N (R ³) ₂,-C (O) R ³,-CO ₂R ³,-SO ₂R ³Or 3-6 unit contain 0-2 heteroatomic aromatic nucleus or non-aromatic ring, described heteroatoms is independently selected from nitrogen, oxygen or sulphur.More preferred substituents on the described ring is selected from: the optional C that replaces _1-4Aliphatic group, NH ₂, NH (C _1-4Aliphatic group), N (C _1-4Aliphatic group) ₂, optional phenyl, the CO that replaces ₂(C _1-4Aliphatic group) or SO ₂(C _1-4Aliphatic group).Most preferred substituting group on the described ring is selected from: methyl, ethyl, methylsulfonyl, (CH ₂) ₂SO ₂CH ₃, cyclopropyl, CH ₂Cyclopropyl, (CH ₂) ₂OH, CO ₂The tertiary butyl, CH ₂Phenyl, phenyl, NH ₂, NH (CH ₃), N (CH ₃) ₂, (CH ₂) ₂NH ₂, (CH ₂) ₂Morpholine-4-base, (CH ₂) ₂N (CH ₃) ₂, sec.-propyl, propyl group, the tertiary butyl, (CH ₂) ₂CN or (CH ₂) ₂C (O) morpholine-4-base.

More preferably, the N (R of formula I ' ¹) ₂The ring that forms is slightly alkyl, piperidyl, morpholine-4-base, thiomorpholine-4-base, piperazine-1-base, diazacyclo heptyl or a tetrahydro isoquinolyl of pyrrole, and each ring is all randomly replaced by one or two substituting group that is independently selected from following radicals: methyl, ethyl, methylsulfonyl, (CH ₂) ₂SO ₂CH ₃, cyclopropyl, CH ₂Cyclopropyl, (CH ₂) ₂OH, CO ₂The tertiary butyl, CH ₂Phenyl, phenyl, NH ₂, NH (CH ₃), N (CH ₃) ₂, (CH ₂) ₂NH ₂, (CH ₂) ₂Morpholine-4-base, (CH ₂) ₂N (CH ₃) ₂, sec.-propyl, propyl group, the tertiary butyl, (CH ₂) ₂CN or (CH ₂) ₂C (O) morpholine-4-base.

Use the preferred compound in the formula I compound of method of the present invention preparation to have general formula V:

Or its pharmaceutically acceptable derivates or salt, wherein:

R ⁵Be selected from hydrogen or C _1-4Aliphatic group;

R ⁶Be selected from C _1-3Aliphatic group; And

R ⁷Be selected from C _1-4Aliphatic group.

The preferred R of formula V ⁵Group is selected from: hydrogen, methyl, ethyl, the tertiary butyl, propyl group, cyclopropyl, cyclopropyl methyl or sec.-propyl.The preferred R of formula V ⁵Group is selected from hydrogen or methyl.The most preferred R of formula V ⁵Group is a methyl.

The preferred R of formula V ⁶Group is selected from methyl, ethyl or cyclopropyl.The preferred R of formula V ⁶Group is methyl or cyclopropyl.The most preferred R of formula V ⁶Group is a methyl.

The preferred R of formula V ⁷Group is selected from methyl, ethyl, the tertiary butyl or cyclopropyl.The preferred R of formula V ⁷Group is selected from ethyl or cyclopropyl.The most preferred R of formula V ⁷Group is a cyclopropyl.

According to another embodiment, the present invention relates to formula V compound:

Or its pharmaceutically acceptable derivates or salt, wherein:

R ⁵Be selected from hydrogen or C _1-4Aliphatic group;

R ⁶Be selected from C _1-3Aliphatic group; And

R ⁷Be selected from C _1-4Aliphatic group; Its condition is that described compound is not N-{4-[4-(4-methyl-piperazine-1-yl)-6-(5-methyl-2H-pyrazole-3-yl amino)-pyrimidine-2-base sulfane base]-phenyl }-propionic acid amide.

The preferred R of formula V ⁵Group is selected from: hydrogen, methyl, ethyl, the tertiary butyl or sec.-propyl.The preferred R of formula V ⁵Group is selected from hydrogen or methyl.The most preferred R of formula V ⁵Group is a methyl.

Formula V compound belongs to the compound of record among the open WO 02/057259 of PCT.But the applicant has been found that compound of the present invention has the potentiality as Aurora protein kinase and/or FLT-3 kinases inhibitor surprising and unexpected increase.

Explanation in the demonstrative structure table 1 below of formula V compound.

Table 1

Explanation in other the exemplary compound of the formula I table 2 below of prepared according to the methods of the invention.

The exemplary compound of table 2 formula I

Method of the present invention is preferably used for preparing the compound of selecting from table 1 and 2.Method of the present invention is more preferably used in the compound that preparation is selected from table 1.

According to another embodiment, the invention provides the compound of formula II, formula III or formula IV:

Or its pharmacy acceptable salt, wherein R ^x, R ^y, L ¹, L ², L ³, T, R ^Z2Define as above with Q and their preferred embodiment.

According to an embodiment preferred, the invention provides formula II intermediate.

According to another embodiment preferred, the invention provides the formula III intermediate.

According to another embodiment preferred, the invention provides formula IV intermediate.

According to another embodiment, the invention provides a kind of composition, it contains compound of the present invention or pharmaceutically acceptable derivates and pharmaceutically acceptable carrier, assistant agent or vehicle.The amount of compound in composition of the present invention should reach proteolytic enzyme, particularly Aurora and/or the FLT-3 kinases that can suppress effectively among biological sample or the patient with detecting.Preferably, composition of the present invention is made the preparation of using to the patient who needs said composition easily.More preferably, composition of the present invention is made the preparation to patient's dosage forms for oral administration.

As used herein, term " patient " is meant animal, preferred mammal, and optimum is chosen.

Term " pharmaceutically acceptable carrier, assistant agent or vehicle " refers to nontoxic carrier, assistant agent or vehicle, and it can not destroy the pharmacological activity of the compound of preparing with it.The pharmaceutically acceptable carrier that can in composition of the present invention, use, assistant agent or vehicle include but not limited to: ion-exchanger, aluminum oxide, aluminum stearate, Yelkin TTS, serum protein, human serum albumin for example, buffer reagent, phosphoric acid salt for example, glycine, Sorbic Acid, potassium sorbate, the glyceride mixture of the saturated vegetable fatty acid of part, water, salt or ionogen, for example protamine sulfuric ester, Sodium phosphate dibasic, potassium hydrogen phosphate, sodium-chlor, zinc salt, silica gel, Magnesium Trisilicate, polyvinylpyrrolidone, based on cellulosic material, polyoxyethylene glycol, Xylo-Mucine, polyacrylic ester, wax, polyethylene-polyoxypropylene-segmented copolymer, polyoxyethylene glycol and wool grease.

" can suppress " to refer to contain the sample of described composition and protein kinase with detecting and contain the measurable change that is equal to the protein kinase activity between the sample that protein kinase does not still contain described composition as term used herein.

" pharmaceutically acceptable derivates or salt " refers to any nontoxic salt, the ester of compound of the present invention, salt or other derivative of ester, after using to the receptor, it can be directly or provides compound of the present invention or its to have the active meta-bolites of inhibition or resistates indirectly.As used herein, term " it has the active meta-bolites of inhibition or resistates " refers to that its meta-bolites or resistates also are the inhibitor of Aurora and/or FLT-3 protein kinase.

According to another embodiment, the invention provides the method for the pharmacy acceptable salt of preparation formula I, I ' or V compound, it comprises the step that formula I, I ' or V compound according to the preparation of the method for present method are transformed into the ideal pharmacy acceptable salt.This transformation is well known in the art.Referring to, usually, " Advanced Organic Chemistry, " Jerry March, 4 ^ThEd., John Wiley and Sons, N.Y. (1992).

The pharmacy acceptable salt of compound of the present invention comprises the salt that derives from pharmaceutically acceptable inorganic or organic bronsted lowry acids and bases bronsted lowry.The example of suitable hydrochlorate comprises: acetate, adipate, alginates, aspartate, benzoate, benzene sulfonate, hydrosulfate, butyrates, Citrate trianion, camphorate, camsilate, cyclopentane propionate, digluconate, dodecyl sulfate, ethane sulfonate, formate, fumarate, the glucose enanthate, glycerophosphate, oxyacetate, Hemisulphate, enanthate, hexanoate, hydrochloride, hydrobromate, hydriodate, the 2-isethionate, lactic acid salt, maleate, malonate, mesylate, the 2-naphthalenesulfonate, nicotinate, nitrate, oxalate, palmitate, pectinic acid salt (pectinate), persulphate, 3-phenylpropionic acid salt, phosphoric acid salt, picrate, pivalate, propionic salt, salicylate, succinate, vitriol, tartrate, thiocyanate, tosylate and undecylate.Other acid is oxalic acid for example, though himself be pharmaceutically unacceptable, can be used as the intermediate that obtains compound of the present invention and their pharmaceutically-acceptable acid addition in the process of preparation salt.

The salt that derives from suitable alkali comprises basic metal (for example sodium and potassium) salt, alkaline-earth metal (for example magnesium) salt, ammonium salt and N ⁺(C _1-4Alkyl) ₄Salt.The present invention also predicts the quaterisation of any alkaline nitrogen-containing group of compound disclosed herein.Can obtain soluble or dispersible products in water or oil by such quaterisation.

Following table 3 has been illustrated the representational salt of formula V compound of the present invention.

The representational salt of table 3 formula V compound

Composition of the present invention can per os ground, the stomach and intestine other places, suck spray method, partly, rectum ground, through nasally, cheek, vagina ground or use by the container of implantation.That term used herein " parenteral " comprises is subcutaneous, intravenous, intramuscular, IA, in the synovial bursa, in intrasternal, the sheath, the liver, intralesional with injection encephalic or inculcate technology.Preferably, use composition per os ground, endoperitoneal or intravenously.The aseptic injection form of composition of the present invention can be water-based or butyrous suspension.Can be according to technology known in the art, use suitable dispersion agent or wetting agent and suspension agent to prepare these suspension.Aseptic injection preparation can also be at nontoxic injection acceptable diluent or aseptic injectable solution or the suspension in the solvent, for example solution in 1,3 butylene glycol.Acceptable medium that can adopt and solvent are water, Ringer's solution and isotonic sodium chlorrde solution.In addition, aseptic non-volatility oils is routinely as solvent or suspension medium.

For this purpose, the fixed oil of any gentleness can use, and comprises synthetic list-or two-glyceryl ester.Lipid acid, for example oleic acid and its glyceride derivative can be used as the preparation that natural pharmaceutically acceptable oil is used for injection, for example sweet oil or Viscotrol C, particularly their polyoxy ethylization form.These butyrous solution or suspension can also contain the pure thinner or the dispersion agent of long-chain, for example carboxymethyl cellulose or similarly usually at the dispersion agent that uses when (comprising milk sap and suspension) of the pharmaceutically acceptable formulation of preparation.For the purpose of preparing, can also use other tensio-active agent commonly used, for example tween, Span and other emulsifying agent or the bioavailability toughener of when producing pharmaceutically acceptable solid, liquid or other formulation, using always.

Pharmaceutically acceptable composition of the present invention can be with the acceptable forms administration of any per os ground, and this includes but not limited to capsule, tablet, waterborne suspension or solution.For the tablet that per os uses, carrier commonly used comprises lactose and W-Gum.Also typically add lubricant, for example Magnesium Stearate.For oral capsule form, the available thinner comprises lactose and dried corn starch.When needs used the waterborne suspension per os, activeconstituents and emulsifying agent and suspension agent were combined.If desired, can also add some sweetener, correctives or toning agent.

Perhaps, pharmaceutically acceptable composition of the present invention can be used with the suppository form of rectal administration.They can prepare by medicine and suitable non-stimulated vehicle are mixed mutually, described vehicle at room temperature be solid-state but under rectal temperature for liquid, therefore will in rectum, melt and discharge medicine.Such material comprises theobroma oil, beeswax and polyoxyethylene glycol.

Pharmaceutically acceptable composition of the present invention can also topical application, when the treatment target position comprises by easy approaching zone of topical application or organ, comprises illness in eye, tetter or lower intestinal tract disease especially.Can easily prepare at the suitable topical formulations in these zones or the organ.

The topical application of lower intestinal tract can realize with rectal suppository (on seeing) or suitable enema agent.Can also use partial transdermal plaster.

For topical application, pharmaceutically acceptable composition can be made suitable paste, and it contains and suspends or be dissolved in active ingredient in one or more carriers.The carrier that is used for topical application compound of the present invention includes but not limited to mineral oil, Albolene, white vaseline, propylene glycol, polyethylene, polyoxypropylene compound, emulsifying wax and water.Perhaps, pharmaceutically acceptable composition can be made suitable lotion or emulsion, and it contains and suspends or be dissolved in active ingredient in one or more pharmaceutically acceptable carriers.Suitable carriers includes but not limited to mineral oil, sorbitan monostearate, polysorbate60, whale ester type waxes, hexadecanol, 2-Standamul G, phenylcarbinol and water.

Use for eye, pharmaceutically acceptable composition can be made the suspension of littleization, it or preferably is formed in solution in isoosmotic, as the to transfer pH Sterile Saline in isoosmotic, as to transfer pH Sterile Saline, can have or not have for example Zephiran chloride of sanitas.Perhaps, for eye usefulness, pharmaceutically acceptable composition can be made paste, for example Vaseline.

Pharmaceutically acceptable composition of the present invention can also or suck by the nose aerosol and use.Such composition can prepare according to the technology that field of pharmaceutical preparations is known, and can make salt brine solution, adopt benzylalcohol or other suitable sanitas, the absorption enhancer that can strengthen bioavailability, fluorocarbon and/or other conventional solubilizing agent or dispersion agent.

More preferably, pharmaceutically acceptable composition of the present invention is to make oral preparations.

Can become with the host of treatment, specific mode of administration with the amount of the The compounds of this invention of the incompatible composition of making single dosage form of vehicle group.Preferably, should to make and make dosage be that the inhibitor of 0.01-100mg/kg body weight/day can be administered to the patient who accepts these compositions to composition.

It should also be understood that, given dose and treatment plan at any particular patients ' will depend on multiple factor, and this comprises activity, age, body weight, general health, sex, diet situation, administration time, discharge rate, drug regimen, treatment doctor's the judgement of the specific compound of employing and the severity of the specified disease that will treat.The amount of compound of the present invention in composition also depends on the specific compound in the composition.

According to specific uncomfortable disease, the disease that will treat or prevent, can also contain other therapeutical agent that is commonly used to treat or prevent these diseases in the composition of the present invention.As used herein, be commonly used to treat or prevent other therapeutical agent of specified disease or uncomfortable disease to be known as " being applicable to disease or the uncomfortable disease that will treat ".

For example, chemotherapeutic or other antiproliferative agents can with combined proliferative disease and the cancer for the treatment of of compound of the present invention.The example of known chemotherapeutic includes but not limited to Gleevec ^TM, Zorubicin, dexamethasone, vincristine(VCR), endoxan, Fluracil, topotecan, taxol, Interferon, rabbit and platinum derivatives.

Other example of the medicine that inhibitor of the present invention can also make up includes but not limited to: the medicine of treatment Alzheimer, for example Aricepe ^_And Excelon ^_Treat Parkinsonian medicine, for example ergot woods, Trihexyphenidyl and amantadine in L-DOPA/ carbidopa, Entacapone, Ropinrole, pramipexole, bromocriptine, the sulphur; Treat the medicine of many sclerosiss (MS), for example beta-interferon (Avonex for example ^_And Rebif ^_), Copaxone ^_And mitoxantrone; The medicine of treatment asthma, for example salbutamol and Singulair ^_Treat schizoid medicine, for example Zyprexa, Wei Sitong, En Ruikang and haloperidol; Antiphlogiston, for example reflunomide, TNF blocker, IL-1RA, azathioprine, endoxan and sulfasalazine; Immunomodulatory and immunosuppressor, for example S-Neoral, tacrolimus, rapamycin, mofetil mycophenolate, Interferon, rabbit, reflunomide, endoxan, azathioprine and sulfasalazine; Neurotrophic factor, for example acetylcholinesterase depressant, MAO inhibitor, Interferon, rabbit, anticonvulsive drug, ion channel blocking agent, Riluzole and antiparkinsonism drug; The medicine of treatment cardiovascular diseases, for example β--blocker, ACE inhibitor, diuretic(s), nitrate, calcium channel blocker and statin; The medicine of treatment hepatopathy, for example reflunomide, Colestyramine, Interferon, rabbit and antiviral drug; Treat hemopathic medicine, for example reflunomide, antileukemia and somatomedin; With the medicine of treatment, the medicine of treatment immunodeficient disease, for example gamma globulin.

Can make up with compound of the present invention and treat the sick and chemotherapeutic of cancer of propagation or other example of other antiproliferative agents includes but not limited to, for example, can comprise operation with the treatment or the carcinostatic agent of creationary carcinostatic agent combination of the present invention, radiotherapy is (but in a few examples, γ-radiation, neutron beam radiotherapy, electron beam radiotherapy, proton therapy, the radio isotope of short range radiotherapy and whole body, only give some instances), endocrinotherapy, biological respinse activator (Interferon, rabbit, interleukin and tumour necrosis factor (TNF) only give some instances), hyperthermia and refrigeration treatment, alleviate the medicine (for example antiemetic) of any side effect and the chemotherapeutic of other permission, include but not limited to alkyl chemical drug (mustargen, Chlorambucil, endoxan, melphalan, ifosfamide), metabolic antagonist (methotrexate), purine antagonist and pyrimidine antagonist (6-mercaptopurine, 5 FU 5 fluorouracil, cytosine arabinoside, gemcitabine), spindle poison (vinealeucoblastine(VLB), vincristine(VCR), vinorelbine, taxol), podophyllotoxin (Etoposide, irinotecan, topotecan), microbiotic (Zorubicin, bleomycin, mitomycin), nitrosourea (carmustine, lomustine), mineral ion (Platinol, carboplatin), enzyme (asparaginase) and hormone (tamoxifen, leuprorelin acetate, flutamide and megestrol), Gleevec ^TM, Zorubicin, dexamethasone and endoxan.For up-to-date cancer therapy will more fully be described, referring to: http://www.nci.nih.gov/, the tumour medicine tabulation and the The Merck Manual of the FDA approval on http://www.fda.gov/cder/cancer/druglistframe.htm, Seventeenth Ed.1999.Their whole inherences are incorporated by reference hereby.

The amount of other therapeutical agent in composition of the present invention should not surpass and contain this therapeutical agent as the amount of using usually in the independent composition of active components.Preferably, the amount of other therapeutical agent in present disclosed composition is to contain this medicine as about 50%～100% of common consumption in the composition of independent therapeutic activity composition.

According to the another one embodiment, the present invention relates to a kind of method that suppresses Aurora-1, Aurora-2, Aurora-3 and/or FLT-3 kinase activity in the biological sample, it comprises described biological sample with formula V compound or contain the step that described compound compositions contacts.

Term used herein " biological sample " includes but not limited to cell culture or its extract; The slicer material or its extract that obtain from Mammals; With blood, saliva, urine, ight soil, seminal fluid, tears or other body fluid or its extract.

Aurora-1, the Aurora-2, Aurora-3 and/or the FLT-3 kinase activity that suppress in the biological sample can be used for various purpose well known by persons skilled in the art.The example of these purposes includes but not limited to blood transfusion, organ transplantation, biological sample preservation and Bioexperiment.

According to the another one embodiment, the present invention relates to the method for a kind of patient's of inhibition Aurora-1 kinase activity, it comprises to described patient uses formula V compound or contains the step of described compound compositions.

According to the another one embodiment, the present invention relates to the method for a kind of patient's of inhibition Aurora-2 kinase activity, it comprises to described patient uses formula V compound or contains the step of described compound compositions.

According to the another one embodiment, the present invention relates to the method for a kind of patient's of inhibition Aurora-3 kinase activity, it comprises to described patient uses formula V compound or contains the step of described compound compositions.

According to the another one embodiment, the present invention relates to the method for a kind of patient's of inhibition FLT-3 kinase activity, it comprises to described patient uses formula V compound or contains the step of described compound compositions.

According to the another one embodiment, the present invention relates to the method for a kind of patient's of inhibition Aurora-1, Aurora-2, Aurora-3 and FLT-3 kinase activity, it comprises to described patient uses formula V compound or contains the step of described compound compositions.

According to the another one embodiment, the invention provides the method for the severity of a kind of disease of Aurora mediation for the treatment of or alleviating the patient or uncomfortable disease, it comprises to described patient uses formula V compound or contains the step of described compound compositions.

Term used herein " Aurora mediation disease " refer to that known Aurora family protein kinases works therein any disease or other deleterious uncomfortable disease or disease.Such disease or uncomfortable disease include but not limited to melanoma, leukemia or colorectal carcinoma, mastocarcinoma, cancer of the stomach, ovarian cancer, cervical cancer, melanoma, kidney, prostate cancer, lymphoma, neuroblastoma, carcinoma of the pancreas, leukemia and bladder cancer.

According to the another one embodiment, the present invention relates to a kind of treatment patient method for cancer, it comprises the step of using formula V compound or its composition to described patient.

According to the another one embodiment, the present invention relates to the method for a kind of patient's of treatment melanoma, lymphoma, neuroblastoma, leukemia or colorectal carcinoma, mastocarcinoma, lung cancer, kidney, ovarian cancer, carcinoma of the pancreas, kidney, CNS, cervical cancer, prostate cancer or stomach tube cancer, it comprises the step of using formula V compound or its composition to described patient.

According to the another one embodiment, the present invention relates to the method for a kind of patient's of treatment acute myelocytic leukemia (AML), acute lymphoblastic leukemia (ALL), mast cell disease or gastrointestinal stromal tumor (GIST), it comprises the step of using formula V compound or its composition to described patient.

Another aspect of the present invention relates to the mitotic interruption to patient's cancer cells, and it comprises the step of using formula y compound or its composition to described patient.

According to the another one embodiment, the present invention relates to a kind of method for the treatment of or alleviating patient's cancer severity, it comprises with formula V compound or its composition and suppresses the mitotic step that Aurora-1, Aurora-2 and/or Aurora-3 interrupt cancer cells.

In a replacement scheme, method utilization of the present invention does not contain the composition of other therapeutical agent, and it also comprises an other step: use other therapeutical agent separately for described patient.When using these other therapeutical agent separately, they can be before using compound of the present invention, use in order or afterwards.

Embodiment

In order to understand the present invention described herein more fully, the following examples have been set forth.Should be appreciated that these embodiment just are used for task of explanation, and not should be understood to limit by any way the present invention.

Embodiment

General flow chart:

Embodiment 1

4,6-dichloro pyrimidine-2-methyl sulfone (A): according to following basically with people such as Koppell, JOC, 26,1961,792 described method similar methods preparations.

In 20 minutes time, in 4 of 0 ℃ of stirring, 6-two chloro-2-(methyl sulfo-) pyrimidine (50g, 0.26mol) in the solution of methylene dichloride (1L), add metachloroperbenzoic acid (143.6g, 0.64mol).Allow solution temperature rise to room temperature, stirred 4 hours.Mixture is used 50%Na then successively with methylene dichloride (1.5L) dilution ₂S ₂O ₃/ NaHCO ₃Solution (2 * 200ml), sat.NaHCO3 solution (4 * 300ml) and salt solution (200ml) handle dry then (MgSO ₄).Solvent removed in vacuo obtains linen solid, and it is dissolved among the EtOAc (1L) again, uses saturated NaHCO successively ₃Solution (3 * 300ml) and salt solution (100ml) handle dry then (MgSO ₄).Solvent removed in vacuo obtains the title compound (A) (55.6g, 96% productive rate) of white solid. ¹H?NMR?CDCl ₃δ3.40(3H，s，CH ₃)、7.75(1H.s.ArH)。

Embodiment 2

[4-(4 for cyclopropane-carboxylic acid, 6-two chloro-pyrimidine-2-base sulfane bases)-phenyl]-acid amides (C): with compd A (10g, 44.04mmol) and cyclopropane-carboxylic acid (4-sulfydryl-phenyl)-acid amides (B, 8.51g, 44.04mmol) suspension vacuum outgas in the trimethyl carbinol (300ml), use nitrogen wash then.Mixture stirred 1 hour in nitrogen atmosphere in 90 ℃, then solvent removed in vacuo.Resistates is dissolved into (600ml) in the vinyl acetic monomer, with the solution washing of salt of wormwood and sodium-chlor.Organic extraction is condensed into small volume and crystallization through dried over mgso.Collect the product C (11.15g, 74%) of clear crystal shape. ¹H-NMR?DMSO-d ⁶，δ0.82-0.89(4H，m)，1.80-1.88(1H，m)，7.55(2H，d)，7.70-7.76(3H，m)，10.49(1H，s)；M+H，340。

Embodiment 3

Cyclopropane-carboxylic acid 4-[4-chloro-6-(5-methyl-2H-pyrazole-3-yl amino)-pyrimidine-2-base sulfane base]-phenyl } acid amides (D): with diisopropyl ethyl amine (0.614ml, 3.53mmol) and sodium iodide (530mg, 3.53mmol) processing Compound C (1.0g, 2.94mmol) and 3-amino-5-methylpyrazole (314mg, 3.23mmol) mixture in dimethyl formamide (6ml).Mixture stirred 4 hours under nitrogen in 85 ℃, was cooled to room temperature, diluted with vinyl acetic monomer.Solution with water (x4) washing through dried over mgso, is concentrated into 5ml, collects clear crystal after crystallization, obtains title compound D (920mg, 78%). ¹H-NMR?DMSO-d ⁶，δ0.80-0.87(4H，m)，1.77-1.85(1H，m)，1.92(1H，s)，5.24(1H，brs)，6.47(1H，brs)，7.55(2H，d)，7.70-7.80(2H，m)，10.24(1H，s)，10.47(1H，s)，11.92(1H，s)。

Embodiment 4

Cyclopropane-carboxylic acid 4-[4-(4-methyl-piperazine-1-yl)-6-(5-methyl-2H-pyrazole-3-yl amino)-pyrimidine-2-base sulfane base]-phenyl }-acid amides (V-1): handle Compound D (2.373g with N methyl piperazine (10ml), 5.92mmol), mixture stirred 2 hours at 110 ℃.Vacuum is removed unnecessary N methyl piperazine, and resistates is dissolved in the vinyl acetic monomer, with the sodium bicarbonate aqueous solution washing, through dried over mgso, concentrates.Resistates crystallization in methyl alcohol obtains the clear crystal (1.82g, 66%) of purpose product V-1, ¹H-NMR DMSO-d ⁶, (30.81 (4H, d), 1.79 (1H, m), 2.01 (3H, s), 2.18 (3H, s), 2.30 (4H, m), 3.35 (shielded signals), 5.42 (1H, s), 6.0 ₂(1H, brs), 7.47 (2H, d), 7.69 (2H, d), 9.22 (1H, s), 10.39 (1H, s), 11.69 (1H, s).

Embodiment 5

N-{4-[4-(5-methyl-2H-pyrazole-3-yl methyl)-6-(4-propyl group-piperazine-1-yl)-pyrimidine-2-base sulfane base]-phenyl }-propionic acid amide (V-5): successively use N-propyl group piperazine dihydrobromide (887mg, 3.06mmol) and diisopropyl ethyl amine (1.066mL, 6.12mmol) handle ethane formic acid in n-BuOH (5mL) { 4-[4-chloro-6-(5-methyl-2H-pyrazole-3-yl amino)-pyrimidine-2-base sulfane base]-phenyl } acid amides (119mg, 0.306mmol, by preparing with embodiment 1,2 and 3 similar methods).Obtaining mixture stirred 20 hours at 110 ℃.Removal of solvent under reduced pressure with preparation HPLC purifying resistates, obtains title compound. ¹H?NMR(DMSO)：δ1.10(3H，t)，2.05(3H，s)，2.35(2H，d)，3.30(4H，s)，3.70(4H，s)，5.45(1H，s)，6.05(1H，brs)，7.4?5(2H，d)，7.70(2H，d)，9.20(1H，s)，10.05(1H，s)，11.70(1H，brs)。

Embodiment 6

N-[4-(4,6-two chloro-pyrimidine-2-base oxygen)-phenyl]-ethanamide: the sodium hydride with 60% is in mineral oil (176mg, 4.40mmol) in dispersed system handle 4-acetaminophenol (666mg, 4.40mmol) solution in anhydrous THF (40ml) that stirs in envrionment temperature.Reaction mixture was stirred 30 minutes at ambient temperature, add 4 then, and 6-two chloro-2-methane sulfonyl-pyrimidines (1.0g, 4.40mmol).Reaction continues to stir 3 hours, uses NH again ₄The saturated aqueous solution dilution of Cl and EtOAc.Separate organic layer, with the saturated aqueous solution washing of NaCl, through dried over mgso, vacuum concentration then.By column chromatography (silica gel, MeOH: CH ₂Cl ₂, 5: 95) and the purifying resistates obtains the title compound 1.25g of solid state, (95%) ¹H-NMR (400MHz, DMSO-d ₆): δ 2.06 (3H, s), 7.18 (2H, d, J=8.5Hz), 7.62 (2H, d, J=8.5Hz), 10.05 (1H, s), LC-MS:ES+=298.16, ES-=296.18).

Embodiment 7

Cyclopropane-carboxylic acid 4-[4-(4-methyl-4-oxygen-piperazine-1-yl)-6-(5-methyl-2H-pyrazole-3-yl amino)-pyrimidine-2-base sulfane base]-phenyl }-acid amides (V-19): with compound V-1 (1g, 2.1mmol) be suspended in the methylene dichloride (20mL), be cooled to 0 ℃, dichloromethane solution with 10 equal portions mCPBA is handled (each equal portions is by 100mg, and 0.44mmol forms) with 10 minutes interval in 1mlDCM.When every adding was a, solution became brown, and reverts to yellow gradually along with the consumption of mCPBA.In case all raw materials all exhaust, remove solvent with regard to vacuum, obtain yellow oil by preparation HPLC purifying, obtain the title compound (69mg, 7%) of pale solid shape; ¹H NMR (DMSO-d ₆): 0.85-0.91 (4H, m), 1.90 (1H, m), 2.10 (3H, s), 3.10-3.17 (2H, m), 3.25 (3H, s), 3.50-3.66 (4H, m), 3.98 (2H, d), 5.50 (1H, s), 6.11 (1H, brs), 7.56 (2H, d), 7.80 (2H, d), 9.42 (1H, s), 10.50 (1H, s), 11.82 (1H, brs).

Embodiment 8

Cyclopropane-carboxylic acid 4-[4-(4-methyl-piperazine-1-yl)-6-(5-methyl-2H-pyrazole-3-yl amino)-pyrimidine-2-base sulfane base]-phenyl }-acid amides methane sulfonate (V-lii): with compound V-1 (515mg, 1.11mmol) be suspended in the ethanol (80mL) reflux.(106mg, 1.11mmol), reaction mixture continues to reflux 10 minutes to add methanesulfonic in clear liquid.Allow mixture be cooled to room temperature, evaporating solvent is until beginning to form precipitation.Then mixture is chilled to 0 ℃, by filter collecting the precipitation that obtains, vacuum-drying obtains the title compound (290mg, 47%) of white solid; ¹H NMR (400MHz, DMSO-d ₆) 0.81-0.82 (4H, d), 1.82 (1H, m), 2.36 (6H, s), 2.83 (3H, d), 3.03-3.12 (4H, m), 3.40-3.47 (2H, m), 3.79 (brs, OH), 4.14-4.18 (2H, m), 5.50 (1H, s), 6.05 (1H, s), 7.49 (2H, d), 7.72 (2H, d), 9.61 (1H, s), 10.41 (1H, brs), 10.80 (1H, s).

Embodiment 9

Listed following compound is the method according to this invention and prepares with the described similar method of top embodiment 1-8 basically in the table 4 below.The characteristic of these compounds is summarised in the following table 4, and this comprises ¹H NMR, fusing point (m.p.) and mass spectrum (MS) data.

Except as otherwise noted, the note described in the table 4 ¹H NMR is from deuterated dimethyl sulfoxide (DMSO) (dmso-d in 400MHz ₆) obtain.

The characteristic of table 4 representative compounds

Bioexperiment

Compound of the present invention can be by in external, the body or the clone experiment as the activity of kinase inhibitor.Experiment in vitro comprises that mensuration is to the kinase activity of activated Aurora and/or FLT-3 enzyme or the inhibition of atpase activity.Experiment is that the ability of inhibitor in conjunction with Aurora and/or FLT-3 quantized in the body of replaceability, this can be by finishing in conjunction with preceding radio-labeled inhibitor, the amount of separating inhibitor/Aurora and/or inhibitor/FLT-3 mixture and measuring bonded radio-labeled thing, perhaps by with new compound on being attached to known radioligand Aurora and/or the competitive assay of FLT-3 incubation finish.Can use any kind of Aurora or the isomer of Aurora, this depends on the Aurora type or the isomer that will suppress.Be set forth in the detailed conditions of using in the enzyme experiment in the following embodiments.

Embodiment 10

Ki when suppressing Aurora measures

Use standard conjugate enzyme experiment people (1998) Protein Sci 7,2249 such as () Fox SCREENED COMPOUND in the following manner suppresses the ability of Aurora.To containing 0.1M HEPES 7.5,10mMMgCl ₂, 1mM DTT, 25mM NaCl, 2.5mM phosphoenolpyruvic acid ester, 300mM NADH, 30mg/ml pyruvate kinase, 10mg/ml serum lactic dehydrogenase, 40mM ATP and 800 μ M peptide (LRRASLG, American Peptide, Sunnyvale, DMSO solution to the final concentration that adds The compounds of this invention in experimental raw damping fluid CA) is 30 μ M.The mixture that obtains was 30 ℃ of incubations 10 minutes.In experiment, reach final concentration 70nM and start reaction by adding 10 μ L Aurora material solutions.(Hercules CA), in 5 minute reading duration, detects the 340nm absorption value at 30 ℃, obtains speed of reaction to use BioRad Ultramark plate reader.Determine the Ki value from the speed of reaction data with the variation of inhibitor concentration.

Find that formula V compound of the present invention is the inhibitor of Aurora-1, Aurora-2 and Aurora-3.

Embodiment 11

Ki when suppressing FLT-3 measures

Use the radiation measurement strainer to suppress the active ability of FLT-3 in conjunction with experiment (radiometric filter-bindingassay) SCREENED COMPOUND.This tests supervision ³³P is to substrate poly-(Glu, the integration in Tyr) 4: 1 (pE4Y).Be reflected at and contain 100mM HEPES (pH7.5), 10mM MgCl ₂, 25mM NaCl, 1mM DTT, 0.01%BSA and 2.5%DMSO solution in carry out.In the experiment final concentration of substrate be 90 μ M ATP and 0.5mg/ml pE4Y (all from Sigma Chemicals, St Louis, MO).The final concentration of compound of the present invention is normally between the 0.01 and 5 μ M.Typically, the 10mM DMSO feedstock production serial dilution degree by from experimental compound carries out 12 titration.Reaction is at room temperature carried out.

Two kinds of experimental solutions have been prepared.Solution 1 contains 100mM HEPES (pH7.5), 10mMMgCl ₂, 25mM NaCl, 1mg/ml pE4Y and 180 μ M ATP (each reaction contain 0.3 μ Ci's [γ- ³³P] ATP).Solution 2 contains 100mM HEPES (pH7.5), 10mM MgCl ₂, 25mM NaCl, 2mM DTT, 0.02%BSA and 3nM FLT-3.Experimentize on 96 hole flat boards by mixing per 50 μ l solution 1 and 2.5ml compound of the present invention.Reaction starts with solution 2.After 20 minutes, contain the 20%TCA termination reaction of 0.4mM ATP at the room temperature incubation with 50 μ l.Then all reaction volumes are transferred to and filtered on the flat board, by (Hamden, Harvester 9600 usefulness 5%TCA CT) wash from TOMTEC.(Meriden, CT) analytical integration advances pE4y's by PackardTop Count microplate scintillometer (Packard Top Count MicroplateScintillation Counter) ³³The amount of P.Use the Prism software data processing to obtain IC ₅₀Or Ki.

Find that formula V compound of the present invention is the inhibitor of FLT-3.

Embodiment 12

The IC that in the Colo205 cell experiment, suppresses Aurora ₅₀Measure

Also tested the inhibition of compound on cell proliferation.In this experiment,, 10% fetal bovine serum, L-glutaminate and penicillin/streptomycin solution prepares perfect medium by being joined in RPMI 1640 substratum (Sigma).Colon cancer cell (COLO-205 clone) is joined 96 hole flat boards with the inoculum density of 1.25 * 104 cells/well/1500 μ L.By serial dilution, in perfect medium, prepare the solution of experimental compound, add experimental compound solution (50 μ L) to each hole.

In order to measure maximum propagation, organize in contrast with containing a series of each flat board that is added with the hole of perfect medium (200 μ L).Also in each flat board, add the medium control group.Dull and stereotyped 37 ℃ of incubations 2 days. ³The material solution of H-thymidine (1mCi/mL, Amersham Phamacia UK) is diluted to 20 μ Ci/mL in the RPMI substratum, then the such solution of 25 μ L is joined in each hole.The dull and stereotyped continuation 37 ℃ of incubations 3 hours, results are used liquid scintillation counter measurement then ³The absorption of H-thymidine.

Find that formula V compound of the present invention is the inhibitor of Colo205 cancer cells.

Embodiment 13

In the panel of tumour and normal cell type, measure cell proliferation: ³The H thymidine mixes experiment

Select ³The H thymidine mixes experiment as characterizing the method for measuring cell proliferation preferably.The cell that selection is examined the different tumor types of wide scope from healthy tissues is used for experiment.Many tumour cells can selected reason be that they (for example express high-caliber Aurora albumen, MCF-7, PC3, A375, A549) (referring to people EMBOJ.1998 17 such as section 5.3.5 and Bischoff, 3052-3065) and/or can in nude mouse or nude rat, form tumour (for example, HCT116, MCF-7 and MDA-MB-231).

With the cell of logarithmic growth with compound incubation 96 hours.In order to measure cell proliferation, 3 hours adding 0.5 μ Ci in each hole before experiment finishes ³The H thymidine.Harvested cell washs then, calculates the radioactivity that mixes on Wallac microplate beta-counter.In order to measure to inhibition of proliferation, draw the graph of a relation of cpm and compound concentration, from figure, determine IC ₅₀

Following table 5 has been illustrated the clone of using in above-mentioned cell proliferation experiment.For each clone, measured cell proliferation inhibition and ³The mixing of H thymidine (96 hours time points)

Table 5 clone

The source	Clone
The source	Clone	The knot rectal adenocarcinoma	HCT-116
The knot rectal adenocarcinoma	LS174T	The knot rectal adenocarcinoma	HCT-116
The knot rectal adenocarcinoma	LS174T	Leukemia	HL60
Mammary cancer	MDA-MB-231	Leukemia	HL60
Mammary cancer	MDA-MB-231	Mammary cancer	ZR-75-1
Mammary cancer	MCF-7	Mammary cancer	ZR-75-1
Mammary cancer	MCF-7	Prostate cancer	PC3
Carcinoma of the pancreas	MIA-Pa-Ca-2	Prostate cancer	PC3
Carcinoma of the pancreas	MIA-Pa-Ca-2	Melanoma	A375
The human lymphocyte that primary PHA-stimulates	The PHA protoblast	Melanoma	A375

Although described embodiments more of the present invention, obviously, change other such scheme that these basic embodiment can obtain utilizing Compounds and methods for of the present invention.Therefore, will be appreciated that scope of the present invention is to be defined by the claims, rather than limit by the particular of representing by embodiment.

Claims

1. the method for a preparation I compound:

Wherein:

Among Q and the T each is independently selected from oxygen, sulphur or N (R);

R ^xBe U-R ⁵

R ⁵Be selected from halogen, NO ₂, CN, R or Ar;

R ^yBe-N (R ¹) ₂,-OR ¹Or-SR ¹

Each R ³Be independently selected from R or Ar;

Wherein:

Described suitable medium comprises:

I) suitable solvent; With

Ii) randomly, suitable alkali; And

L ³It is suitable leavings group.

According to the process of claim 1 wherein described formula II compound be by in suitable medium with formula III compound and formula R ^Z1-Q-H compound makes up and prepares:

Wherein:

Described suitable medium comprises:

I) suitable solvent; With

Ii) randomly, suitable alkali; And

L ²It is suitable leavings group.

3. according to the method for claim 2, wherein said formula III compound be by in suitable medium with formula IV compound and formula R ^Z2-T-H compound makes up and prepares:

Wherein:

Described suitable medium comprises:

I) suitable solvent; With

Ii) randomly, suitable alkali; And

L ¹It is suitable leavings group.

4. according to the process of claim 1 wherein L ³Be selected from halogen, the optional aryl sulfonyl that replaces or the optional alkyl sulphonyl that replaces.

5. according to the method for claim 4, L wherein ³Be fluorine, chlorine, bromine, iodine, p-toluenesulfonyl, methane sulfonyl, p-nitrophenyl alkylsulfonyl, to bromophenyl alkylsulfonyl or trifluoromethayl sulfonic acid ester.

6. according to the method for claim 5, L wherein ³Be chlorine or iodine.

7. according to the method for claim 2, L wherein ²Be halogen, the optional aryl sulfonyl that replaces or the optional alkyl sulphonyl that replaces.

8. according to the method for claim 7, L wherein ²Be fluorine, chlorine, bromine, iodine, p-toluenesulfonic esters, methane sulfonate, p-nitrophenyl alkylsulfonyl, to bromophenyl alkylsulfonyl or trifluoromethayl sulfonic acid ester.

9. method according to Claim 8, wherein L ²Be chlorine or iodine.

10. according to the method for claim 3, L wherein ¹Be halogen, the optional aryl sulfonyl that replaces or the optional alkyl sulphonyl that replaces.

11. according to the method for claim 10, wherein L ¹It is the optional alkyl sulphonyl that replaces.

12. according to the method for claim 11, wherein L ¹It is methane sulfonyl.

13. according to the process of claim 1 wherein that Q is N (R).

14. according to the process of claim 1 wherein that T is oxygen or sulphur.

15. according to the method for claim 14, wherein T is a sulphur.

16. according to the process of claim 1 wherein R ^yBe-OR ¹Or-N (R ¹) ₂

17. according to the method for claim 16, wherein R ^yBe-N (R ¹) ₂, wherein:

R ¹Be selected from the monocyclic or first dicyclo of 8-10 of R or 3-7 unit saturated, part is undersaturated or the undersaturated 0-4 of containing heteroatomic ring fully, described heteroatoms is independently selected from nitrogen, oxygen or sulphur, perhaps

Each R ¹All be R, two R form the optional 4-7 unit saturated rings that replaces together on same nitrogen-atoms like this, and it contains 2 other heteroatomss that are independently selected from nitrogen, oxygen or sulphur at the most, and wherein:

Each R ¹Replaced randomly and independently :-R by 4 substituting groups that are selected from following radicals at the most ³,-OR ³,-SR ³,-CN ,-NO ₂, oxo, halogen ,-N (R ³) ₂,-C (O) R ³,-OC (O) R ³,-CO ₂R ³,-SO ₂R ³,-SO ₂N (R ³) ₂,-N (R ³) SO ₂R ³,-C (O) NR (R ³) ,-C (O) N (R ³) ₂,-OC (O) NR (R ³) ,-OC (O) N (R ³) ₂,-NR ³C (O) R ³,-NR ³C (O) N (R ³) ₂Or-NR ³CO ₂R ³

18. according to the method for claim 17, wherein R ^yBe-N (R ¹) ₂, wherein:

Each R ¹Be independently selected from R, wherein R is hydrogen or the optional C that replaces _1-4Aliphatic group.

19. according to the method for claim 17, wherein R ^yBe-N (R ¹) ₂, wherein:

Each R ¹All be R, such two R groups form the optional 4-7 unit saturated rings that replaces together, and it contains 2 other heteroatomss that are independently selected from nitrogen, oxygen or sulphur at the most.

20. according to the method for claim 19, wherein R ^yBe to be selected from tetramethyleneimine-1-base, piperidines-1-base, morpholine-4-base, thiomorpholine-4-base, piperazine-1-base, diazacyclo heptyl or the different isoquinolyl of tetrahydrochysene, wherein each ring is randomly replaced by the substituting group that one or two is independently selected from following radicals: methyl, ethyl, methylsulfonyl, (CH ₂) ₂SO ₂CH ₃, cyclopropyl, CH ₂Cyclopropyl, (CH ₂) ₂OH, CO ₂The tertiary butyl, CH ₂Phenyl, phenyl, NH ₂, NH (CH ₃), N (CH ₃) ₂, (CH ₂) ₂NH ₂, (CH ₂) ₂Morpholine-4-base, (CH ₂) ₂N (CH ₃) ₂, sec.-propyl, propyl group, the tertiary butyl, (CH ₂) ₂CN or (CH ₂) ₂C (O) morpholine-4-base.

21. according to the process of claim 1 wherein R ^Z1Be the monocyclic or first dicyclo of 8-10 of 3-7 unit saturated, part is undersaturated or the undersaturated 0-4 of containing heteroatomic ring fully, described heteroatoms is independently selected from nitrogen, oxygen or sulphur, and wherein said ring is replaced by 3 substituting groups that are selected from following radicals at the most randomly and independently :-R ³,-OR ³,-SR ³,-CN ,-NO ₂, oxo, halogen ,-N (R ³) ₂,-C (O) R ³,-OC (O) R ³,-CO ₂R ³,-SO ₂R ³,-SO ₂N (R ³) ₂,-N (R ³) SO ₂R ³,-C (O) NR (R ³) ,-C (O) N (R ³) ₂,-OC (O) NR (R ³) ,-OC (O) N (R ³) ₂,-NR ³C (O) R ³,-NR ³C (O) N (R ³) ₂Or-NR ³CO ₂R ³

22. according to the method for claim 21, wherein R ^Z1Be the 5-6 unit undersaturated 1-3 of containing heteroatomic ring fully, described heteroatoms is independently selected from nitrogen, oxygen or sulphur, and wherein said ring is replaced by 3 substituting groups that are selected from following radicals at the most randomly and independently :-R ³,-OR ³,-SR ³,-CN ,-NO ₂, oxo, halogen ,-N (R ³) ₂,-C (O) R ³,-OC (O) R ³,-CO ₂R ³,-SO ₂R ³,-SO ₂N (R ³) ₂,-N (R ³) SO ₂R ³,-C (O) NR (R ³) ,-C (O) N (R ³) ₂,-OC (O) NR (R ³) ,-OC (O) N (R ³) ₂,-NR ³C (O) R ³,-NR ³C (O) N (R ³) ₂Or-NR ³CO ₂R ³

23. according to the method for claim 22, wherein R ^Z1Be the optional ring that replaces, it is selected from pyrazoles or the following 5-6 unit ring any one:

24. according to the method for claim 23, wherein R ^Z1Be to contain at the most 2 to be independently selected from-N (R ³) ₂,-OR ³Or C ₁-C ₄The substituent pyrazoles ring of aliphatic group.

25. according to the method for claim 24, wherein R ^Z1Be selected from the pyrazoles ring that a substituting group of methyl, ethyl, propyl group, sec.-propyl, the tertiary butyl, cyclopropyl or phenyl randomly replaces.

26. according to the process of claim 1 wherein R ^Z2It is the optional ring that replaces, described ring be selected from the monocyclic or first dicyclo of 8-10 of 5-6 unit saturated, part is undersaturated or the undersaturated 0-4 of containing heteroatomic ring fully, described heteroatoms is independently selected from nitrogen, oxygen or sulphur, and wherein said ring quilt 3 substituting groups that are independently selected from following radicals at the most randomly replaces :-CN ,-NO ₂,-C (O) R ³,-CO ₂R ³,-C (O) NR (R ³) ,-NR ³C (O) R ³,-N (R ³) ₂,-N (R ³) SO ₂R ³,-NR ³C (O) N (R ³) ₂Or-NR ³CO ₂R ³

27. according to the method for claim 26, wherein R ^Z2Be selected from phenyl, imidazolyl, pyrazolyl, pyridyl, pyridazinyl, pyrazinyl, naphthyl, tetralyl, benzimidazolyl-, benzothiazolyl, quinolyl, quinazolyl, benzo two pyranyls, isobenzofuran, indanyl, indyl, indoline, indazolyl or isoquinolyl, wherein:

R ^Z2Quilt 3 substituting groups that are independently selected from following radicals at the most randomly replaces :-Cl ,-Br ,-F ,-CN ,-CF ₃,-COOH ,-CONHMe ,-CONHEt ,-NH ₂,-NHAc ,-NHSO ₂Me ,-NHSO ₂Et ,-NHSO ₂(n-propyl) ,-NHSO ₂(sec.-propyl) ,-NHCOEt ,-NHCOCH ₂NHCH ₃,-NHCOCH ₂N (CO ₂T-Bu) CH ₃,-NHCOCH ₂N (CH ₃) ₂,-NHCOCH ₂CH ₂N (CH ₃) ₂,-NHCOCH ₂CH ₂CH ₂N (CH ₃) ₂,-NHCO (cyclopropyl) ,-NHCO (sec.-propyl) ,-NHCO (isobutyl-) ,-NHCOCH ₂(morpholine-4-yl) ,-NHCOCH ₂CH ₂(morpholine-4-yl) ,-NHCOCH ₂CH ₂CH ₂(morpholine-4-yl) ,-NHCO ₂(tertiary butyl) ,-NH (cyclohexyl) ,-NHMe ,-NMe ₂,-OH ,-OMe, methyl, ethyl, cyclopropyl, sec.-propyl or the tertiary butyl.

28. according to the method for claim 27, wherein R ^Z2Containing 1 is selected from-NR ³C (O) R ³Substituting group, wherein:

Each R ³Be independently selected from R or Ar, and wherein R is hydrogen or the optional C that replaces _1-4Aliphatic group.

29. according to the process of claim 1 wherein that described suitable solvent is protonic solvent, halohydrocarbon, ether, aromatic hydrocarbon, polar or nonpolar aprotic solvent or its any mixture.

30. according to the method for claim 29, wherein said solvent is C _1-5Alkyl alcohol straight chain or branching, ether or polar or nonpolar aprotic solvent.

31. according to the process of claim 1 wherein that described suitable alkali is selected from organic amine, alkaline earth metal carbonate, alkaline earth metal hydride or alkaline earth metal hydroxides.

32. according to the method for claim 31, wherein said suitable alkali is selected from trialkylamine, yellow soda ash, salt of wormwood, sodium hydride, potassium hydride KH, sodium hydroxide or potassium hydroxide.

33. according to the process of claim 1 wherein that described method is used for preparing the compound that is selected from following table 1 and table 2 compound:

Table 1.

Table 2.