开发了一种由邻氨基苯甲醛容易地一锅合成3-氨基喹啉的方法。通过该方法有效地制备了6,7-二甲氧基-3-氨基喹啉-2-羧酸乙酯,该中间体是制备4-苯胺基-苯并[ b ] [1,5]-萘啶-3-腈的关键中间体。描述了合成4-苯胺基-苯并[ b ] [1,5]-萘啶-3-甲腈和4-苯胺基-苯并[ b ] [1,8]-萘啶-3-甲腈的合成路线
开发了一种由邻氨基苯甲醛容易地一锅合成3-氨基喹啉的方法。通过该方法有效地制备了6,7-二甲氧基-3-氨基喹啉-2-羧酸乙酯,该中间体是制备4-苯胺基-苯并[ b ] [1,5]-萘啶-3-腈的关键中间体。描述了合成4-苯胺基-苯并[ b ] [1,5]-萘啶-3-甲腈和4-苯胺基-苯并[ b ] [1,8]-萘啶-3-甲腈的合成路线
This invention provides compounds of formula 1, having the structure
1
which are useful as inhibitors of protein tyro sine kinase and are antiproliferative agents.
这项发明提供了具有结构1的化合物,这些化合物可作为蛋白酪氨酸激酶的抑制剂,是抗增殖剂。
[EN] TRICYCLIC PROTEIN KINASE INHIBITORS<br/>[FR] INHIBITEURS TRICYCLIQUES DE PROTEINE KINASE
申请人:AMERICAN HOME PROD
公开号:WO2001047892A1
公开(公告)日:2001-07-05
This invention provides compounds of formula (1) which are useful as inhibitors of protein tyrosine kinase and are antiproliferative agents.
本发明提供了一种式子为(1)的化合物,它们可用作蛋白酪氨酸激酶的抑制剂并具有抗增殖作用。
TRICYCLIC PROTEIN KINASE INHIBITORS
申请人:Wyeth
公开号:EP1242382A1
公开(公告)日:2002-09-25
Treatment of CNS disorders using D-amino acid oxidase and D-aspartate oxidase antagonists
申请人:GENSET, S.A.
公开号:US20030166554A1
公开(公告)日:2003-09-04
Compounds that are antagonists of D-amino acid oxidase and D-aspartate oxidase, methods of treating CNS disorders including bipolar disorder, psychosis and schizophrenia using the compounds, and pharmaceutically acceptable compositions that contain the antagonists are disclosed.