发明名称 Pyridine and pyrimidine derivatives and their use as inhibitors of cytokine mediated disease
摘要 This invention concerns a bicyclic compound of Formula (I), wherein: G is N, CH or C(CN); ring X is a 5- or 6- membered fused heteroaryl ring which contains 1, 2, or 3 heteroatoms selected from oxygen, sulphur and nitrogen; m is 0 - 2; R1 is a group such as hydroxy, halo, trifluoromethyl, cyano, mercapto, nitro, amino, carboxy and carbamoyl; each of R2 and R3 is hydrogen, halo, C1-6alkyl, C2-6alkenyl or C2-6alkynyl; R4 is a group such as hydrogen, hydroxy, C1-6alkyl, C1-6alkoxy, amino and N-C1-6alkylamino; R5 is a group such as hydrogen, halo, trifluoromethyl, cyano, nitro, amino and hydroxy, and q is 0 - 4; or a pharmaceutically acceptable salt or an in vivo cleavable ester thereof; processes for its preparation and a pharmaceutical composition containing it.
申请公布号 NZ514042(A) 申请公布日期 2003.10.31
申请号 NZ20000514042 申请日期 2000.03.17
申请人 ASTRAZENECA AB 发明人 CUMMING, JOHN GRAHAM
分类号 C07D473/34;A61K31/519;A61K31/52;A61P1/02;A61P1/04;A61P1/16;A61P7/02;A61P9/00;A61P9/04;A61P9/10;A61P9/12;A61P11/00;A61P11/06;A61P13/12;A61P17/00;A61P17/06;A61P19/00;A61P19/02;A61P19/06;A61P19/10;A61P21/00;A61P25/28;A61P29/00;A61P31/04;A61P31/10;A61P31/12;A61P31/18;A61P35/00;A61P35/04;A61P37/08;A61P43/00;C07D471/04;C07D475/06;C07D495/04;C07D513/04;(IPC1-7):C07D495/04;A61K31/33 主分类号 C07D473/34
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