发明名称 ARYL AND HETEROARYL PURINE COMPOUNDS
摘要 Novel bicyclic condensed pyrimidine compounds having general formula (I) wherein X is -CH2-, -NH-(CH2)n-, -O- (CH2) n- or -S- (CH2) n- in which n is zero or 1; A is a 4,5-fused imidazole ring N-substituted by R3 which is hydrogen, C1-C4 alkyl or benzyl, or A is a 2,3-fused pyridine ring C-substituted by R4 which is hydrogen, C1-C4 alkyl, C1-C4 alkoxy, halogen or NR5R6 in which each of R5 and R6 independently is H or C1-C4 alkyl; B is a bicyclic ring chosen from tetralin, indane and 2-oxindole; each of R1 and R2, independently, is hydrogen, C1-C4 alkyl, halogen, hydroxy, C1-C4 alkoxy, C1-C4 alkoxycarbonyl, nitro, cyano or CF3; and the pharmaceutically acceptable salts thereof; and wherein, when at the same time, A is pyridine and B is a tetralin ring, R4 is H, C1-C4 alkyl, C1-C4 alkoxy or halogen and X is as defined above, then each of R1 and R2 is other than H; and wherein, when at the same time, A is imidazole, X is -NH-(CH2)n- as defined above, and B is an indan ring unsubstituted or substituted by one or more of halogen, hydroxy, C1-C4 alkoxy and nitro, then R3 is other than C1-C4 alkyl or benzyl, are provided. Compounds of the formula (I) may be used as tyrosine kinase inhibitors.
申请公布号 CA2209598(C) 申请公布日期 2005.06.07
申请号 CA19962209598 申请日期 1996.10.14
申请人 PHARMACIA & UPJOHN SPA 发明人 BALLINARI, DARIO;BRASCA, MARIA GABRIELLA;LONGO, ANTONIO;BUZZETTI, FRANCO
分类号 A61K31/505;A61K31/52;A61K31/522;A61P25/28;A61P35/00;A61P35/02;A61P37/06;A61P43/00;C07D471/04;C07D473/00;C07D473/30;C07D473/34;C07D473/38;(IPC1-7):C07D471/04 主分类号 A61K31/505
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