2-amino-3-nitro-6-methoxyquinoline 在
钯 作用下,
以
tetrahydrofuran methanol 为溶剂,
反应 0.5h,
以0.38 g of the title compound are obtained as light yellow solid的产率得到2,3-diamino-6-methoxyquinoline
参考文献:
名称:
Imidazo[4,5-b]quinoline-derivatives and their use as no-synthase inhibitors
[EN] IMIDAZO[4,5-B]QUINOLINE-DERIVATIVES AND THEIR USE AS NO-SYNTHASE INHIBITORS<br/>[FR] DERIVES DE IMIDAZO[4,5-B]QUINOLINE ET LEUR UTILISATION EN TANT QU'INHIBITEURS DE NO-SYNTHASE
申请人:ALTANA PHARMA AG
公开号:WO2004076451A1
公开(公告)日:2004-09-10
The compounds of formula I In which R1, R2, R3 and A have the meanings as given In the description are novel effective INOS Inhibitors.
式I中的化合物,其中R1、R2、R3和A的含义如描述中所述,是新颖有效的iNOS抑制剂。
IMIDAZO 4,5-B QUINOLINE-DERIVATIVES AND THEIR USE AS NO-SYNTHASE INHIBITORS
申请人:ALTANA Pharma AG
公开号:EP1599473B1
公开(公告)日:2006-09-20
US7390819B2
申请人:——
公开号:US7390819B2
公开(公告)日:2008-06-24
Imidazo[4,5-b]quinoline-derivatives and their use as no-synthase inhibitors
申请人:Martin Thomas
公开号:US20060160839A1
公开(公告)日:2006-07-20
The compounds of formula I
in which R1, R2, R3 and A have the meanings as given in the description are novel effective INOS inhibitors.