发明名称 Pyrrolo{2,3d}pyrimidines and their use as tyrosine kinase inhibitors
摘要 Compounds of formula I including pharmaceutically acceptable salts thereof in which R1 represents hydrogen, 2-phenyl-1,3-dioxan-5-yl, a C1-6 alkyl group, a C3-8 cycloalkyl group, a C5-7 cycloalkenyl group or an (optionally substituted phenyl)C1-6 alkyl group wherein the alkyl, cycloalkyl and cycloalkenyl groups are optionally substituted by one or more groups of formula ORA in which RA represents H or a C1-6 alkyl group provided that a group of formula ORA is not located on the carbon attached to nitrogen; R2 represents hydrogen, a C1-6 alkyl group, a C3-8 cycloalkyl group, halo, hydroxy, an (optionally substituted phenyl)C1-6 alkyl group, optionally substituted phenyl or R4; and R3 represents a group of formula (a) in which the phenyl ring is additionally optionally substituted and A represents NH, O, NHSO2, SO2NH, a C1-4 alkylene chain, NHCO, NHCO2, CONH, NHCONH, CO2 or S(O)p in which p is 0, 1 or 2, or A is absent and R5 is attached directly to the phenyl ring; and R5 represents optionally substituted phenyl and, additionally, when A is absent R5 represents a) a phthalimido group optionally substituted by halo or b) a pyrazolylamino group in which the pyrazole ring is optionally substituted by one or more of the following: hydroxy or optionally substituted phenyl; R4 represents a heterocyclic group; are described which are useful in treating proliferative diseases and disorders of the immune system in mammals. Processes to prepare these compounds and pharmaceutical compositions containing these compound are also described.
申请公布号 AU6829398(A) 申请公布日期 1998.10.12
申请号 AU19980068293 申请日期 1998.03.09
申请人 KNOLL AKTIENGESELLSCHAFT 发明人 DAVID JOHN CALDERWOOD;DAVID NORMAN JOHNSTON;PAUL RAFFERTY;HELEN LOUISE TWIGGER;RAINER MUNSCHAUER;LEE ARNOLD
分类号 A61K31/519;A61P35/00;A61P37/02;A61P43/00;C07D487/04 主分类号 A61K31/519
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