[EN] SUBSTITUTED ARYL-AMINE DERIVATIVES AND METHODS OF USE<br/>[FR] DÉRIVÉS AMINÉS À SUBSTITUTION ARYLE ET PROCÉDÉS D'UTILISATION
申请人:AMGEN INC
公开号:WO2006012374A1
公开(公告)日:2006-02-02
The present invention provides classes of compounds, including-their pharmaceutically acceptable derivatives, useful for treating angiogenesis and related diseases such as cancer. Formula I and II wherein R is a 9- or 10-membered heterocyclyl ring selected from 7-isoquinolinyl,..2-methyl-3-oxo-2,3-dihydroindazol-6-yl, [1,6]-naphthydrin-3-yl, [1,7]-naphthydrin-2-yl, 1-oxo-2,3-dihydrobenzofuran-4-yl, 3-oxo-2,3-dihydrobenzofuran-5-yl, dihydro-benzodioxinyl, 6-quinazolinyl, 2-amino-6-quinazolinyl, 4-methylamino-6-quinazolinyl, 2,4-diamino-6 quinazolinyl, 3-oxo-3,4-dihydro-1,4-benzoxazin-6-yl, 2,2-difluoro-l;3-benzodioxol-5-yl and 2,2,3,3 tetrafluoro-2,3-dihydro-l,4-benzodioxin-6-yl, each of which is optionally substituted with one or more substituents selected from halo, haloakyl, C1-6 alkyl, C2-8 alkenyl, C2-8 alkynyl, N-dimethylamino-C1-6-alkyl, N-dimethylamino-C1-6-alkoxy, amino, alkyl-carbonylamino, morpholino-sulfonyl, amino-sulfonyl, oxazolyl, pyrrolyl,4 morpholinyl, carboxyl, cyano, and acetyl; wherein R1 in formula I is selected from unsubstituted or substituted phenyl, 5-6 membered heteroaryl, 9-10 membered bicyclic heterocyclyl and 11-14 membered tricyclic heterocyclyl, and R1 in formula II is selected from specific bicyclic heterocycles.
本发明提供了一类化合物,包括其药用可接受的衍
生物,用于治疗血管生成和相关疾病,如癌症。其中R为从7-
异喹啉基、
2-甲基-3-
氧代-2,3-二
氢吲哚-6-基、[1,6]-
萘啶-3-基、[1,7]-
萘啶-2-基、1-
氧代-
2,3-二氢苯并呋喃-4-基、3-
氧代-
2,3-二氢苯并呋喃-5-基、二
氢苯并二
氧杂环基、6-
喹唑啉基、2-
氨基-6-
喹唑啉基、4-甲
氨基-6-
喹唑啉基、
2,4-二
氨基-6-
喹唑啉基、3-
氧代-3,4-二
氢-1,4-
苯并噁嗪-6-基、
2,2-二
氟-1,3-
苯并二
氧杂环-5-基和
2,2,3,3-四
氟-2,3-二
氢-1,4-
苯并二
氧杂环-6-基中选择的9-或10-成员杂环基,其中每个基可选择地被一个或多个来自卤素、卤代烷基、C1-6烷基、C2-8
烯基、C2-8炔基、N-
二甲氨基-C1-6-烷基、N-
二甲氨基-C1-6-烷
氧基、
氨基、烷基-羰基
氨基、
吗啉磺酰基、
氨基磺酰基、
噁唑基、
吡咯基、
吗啉基、羧基、
氰基和
乙酰基的取代基取代;其中式I中的R1从未取代或取代的
苯基、5-6成员杂芳基、9-10成员双环杂环基和11-14成员
三环杂环基中选择,式II中的R1从特定的双环杂环基中选择。