发明名称 Alkoxy pyrazoles as soluble guanylate cyclase activators
摘要 The present invention relates to compounds of formula (I):; and pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, R5, R6 and R7 are as defined herein. The invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes.
申请公布号 US8906904(B2) 申请公布日期 2014.12.09
申请号 US201314016452 申请日期 2013.09.03
申请人 Boehringer Ingelheim International GmbH 发明人 Brenneman Jehrod Burnett;Ginn John;Lowe Michael D.;Sarko Christopher Ronald;Tasber Edward S.;Zhang Zhonghua
分类号 C07D401/14;C07D405/14;C07D498/04 主分类号 C07D401/14
代理机构 代理人 Morris Michael P.;Lazer Edward S.
主权项 1. A compound of the formula I wherein: A is a 5-7 membered saturated heterocyclyl group containing one nitrogen and optionally one oxygen, wherein one carbon of said heterocyclyl group is optionally substituted with one or two groups selected from C1-3alkyl and oxo; R1 is C1-4 alkyl optionally substituted with a methoxy group; R2 is selected from H, F, Cl, C1-3alkyl, —CN, —OMe and —CF3; R3 is selected from H and —CH3; R4 is selected from H, F, —CH3 and —OMe; R5 is selected from H, Cl, —CH3, —CH2CH3, —CF3, F, and —OMe; R6 is bonded to the nitrogen on A and is selected from H, C1-6alkyl, —(CH2)nC3-6cycloalkyl, —C(O)C1-6alkyl, —(CH2)n heterocyclyl, —(CH2)n aryl —(CH2)n heteroaryl, —SO2aryl, SO2C1-6alkyl wherein said C1-6alkyl, —(CH2)n heterocyclyl, —(CH2)n cycloalkyl, —(CH2)n aryl and —(CH2)n heteroaryl are optionally substituted with one to four groups independently selected from C1-3alkyl, halogen, C1-3alkoxy, —CF3, —OH, oxo, —(CH2)1-3O(CH2)2-3OH, and —SO2CH3; R7 is selected from H, —CH3, —CH2CH3, —CF3, F, and —CN; n is 0, 1 or 2 or a salt thereof.
地址 Ingelheim am Rhein DE