(5-bromopyridin-3-yl)(7-tert-butyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)methanone 、 氨 在
Copper sulfate pentahydrate盐酸 、 二氯甲烷 、 magnesium sulfate 作用下,
反应 34.0h,
以to afford the title compound as a white solid in 49% yield, 240 mg的产率得到(5-aminopyridin-3-yl)(7-tert-butyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)methanone
The present invention relates to compounds of Formula (I)
and their pharmaceutically acceptable salts, wherein the substituents are as described herein, and their use in medicine, in particular as Trk antagonists.
PYRROLO [2, 3 -D]PYRIMIDINE DERIVATIVES AS INHIBITORS OF TROPOMYOSIN- RELATED KINASES
申请人:Pfizer Limited
公开号:EP2694509A1
公开(公告)日:2014-02-12
PYRROLO[2,3-D]PYRIMIDINE DERIVATIVES AS INHIBITORS OF TROPOMYOSIN-RELATED KINASES
申请人:Pfizer Limited
公开号:EP2694509B1
公开(公告)日:2016-05-18
US8846698B2
申请人:——
公开号:US8846698B2
公开(公告)日:2014-09-30
[EN] PYRROLO [2, 3 -D] PYRIMIDINE DERIVATIVES AS INHIBITORS OF TROPOMYOSIN- RELATED KINASES<br/>[FR] DÉRIVÉS DE PYRROLO-[2,3-D]PYRIMIDINE EN TANT QU'INHIBITEURS DES KINASES ASSOCIÉES À LA TROPOMYOSINE
申请人:PFIZER LTD
公开号:WO2012137089A1
公开(公告)日:2012-10-11
The present invention relates to compounds of Formula (I) and their pharmaceutically acceptable salts, wherein the substituents are as described herein, and their use in medicine, in particular as Trk antagonists.