发明名称 AZAINDOLE DERIVATIVES AS MULTI KINASE INHIBITORS
摘要 The present invention relates to compounds of the following formula (I) and/or the pharmaceutically acceptable addition salts, solvates, enantiomers, diastereoisomers thereof, as well as mixtures thereof. The subject matter of the present invention thus also includes the preparation of compounds of formula (I), their uses, in particular in the inhibition of protein kinases which are implicated for example in numerous diseases such as cancers or immune system disorders.;
申请公布号 US2015353539(A1) 申请公布日期 2015.12.10
申请号 US201314655609 申请日期 2013.12.30
申请人 ORIBASE PHARMA 发明人 CHEVE Gwénaël;DAYDE-CAZALS Bénédicte;FAUVEL Bénédicte;BORIES Cédric;YASRI Abdelaziz
分类号 C07D471/04;G01N33/574 主分类号 C07D471/04
代理机构 代理人
主权项 1. Compound of the following formula (I):(I) characterized in that, R1 is a C1-C6 alkyl group, a —NR4R5 group, or an —OR6 group, R4, R5 and R6 are independently a hydrogen atom, and/or C1-C6 alkyl group, X is chosen from a group consisting of: —C*(R7R8)-N(R9)-C(R10R11)-,—C*(R7R8)-N(R9)-C(O)—,—C*(R7R8)N(R9)-,—C*(R7R8)O—,—O*C(R7R8)-,—C*(R7R8)S—,—S*C(R7R8)-,—C*(R7R8)C(R9R10)-,—C*(O)NH—,—C*(S)NH—,—C*(R7)=C(R8)-,—C*(R7)=N—, and—N*(R7)-C(R8R9)-C(R10R11)-wherein R7, R8, R9, R10 and R11 are independently a hydrogen atom, and/or C1-C6 alkyl, and the atoms labeled with a “*” are linked to the carbon labeled with a “*” in formula (I), R2 is a hydrogen atom, a C1-C6 alkyl group or a halogen atom, Y is chosen from a group consisting of HNC(O), HNC(S), HNSO2, HNC(O)CH2, HNC(S)CH2, HNC(O)NH, HNC(S)NH, CH2NHC(O), C(O)NH, CH2NHC(S) and C(O)NHCH2, and R3 is chosen from a group consisting of: an aryl, group mono or polysubstituted with: a hydroxyl,a halogen,a C1-C6 alkyl-amine,a C1-C6 alkoxy,an amine substituted by a heteroaryl said heteroaryl optionally monosubstituted by a methyl- a C1-C6 trifluoroalkoxy,a C1-C6 alkyl,a C1-C6 trifluoroalkyl,a heteroaryl group optionally monosubstitued by a methylan aliphatic heterocycle, optionally substituted by a methyl group, a hydroxyl group, an amine group, —NHCH3, or —N(CH3)2,a C1-C6 alkyl substituted by a heterocycle, wherein said heterocycle is optionally substituted by a methyl group, a hydroxyl group, an amine group, —NHCH3, or —N(CH3)2, and/orthe fragment: a heteroaryl group, andnon aromatic monosubstituted cyclic group,and/or the pharmaceutically acceptable addition salts, solvates, Z or E isomers, enantiomers, diastereoisomers thereof, as well as mixtures thereof.
地址 Montpellier FR