发明名称 RHO KINASE INHIBITORS
摘要 The invention relates to inhibitors of ROCK1 and/or ROCK2. Also provided are methods of treating diseases and disorders involving inhibiting ROCK1 and/or ROCK2.
申请公布号 US2015252025(A1) 申请公布日期 2015.09.10
申请号 US201314431936 申请日期 2013.10.07
申请人 KADMON CORPORATION 发明人 Poyurovsky Masha;Kim Ji-In;Liu Kevin;Zanin-Zhorov Alexandra
分类号 C07D403/12;C07D409/14;C07D239/42;C07D403/14 主分类号 C07D403/12
代理机构 代理人
主权项 1. A compound of Formula XVI: or pharmaceutically acceptable salt thereof, wherein: R13 and R14 are independently selected from the group consisting of H, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, —(C1-C6 alkyl)-O—(C1-C6 alkyl), heteroaryl, C3-C7 cycloalkyl, a three to twelve membered heterocyclic or aromatic ring containing up to 3 heteroatoms, each of which may be optionally substituted by from 1 to 3 substituents independently selected from halo, oxo, C1-C6 alkyl, C2-C6, alkenyl, C3-C7 cycloalkyl, C1-C6 alkoxy, CN and C1-C3 perfluoro alkyl;or R13 and R14 may be taken together form a three to twelve membered heterocyclic ring having up to 3 heteroatoms which is optionally substituted by from 1 to 3 substituents independently selected from halo, C1-C6 alkyl, C2-C6, alkenyl, C1-C6 alkoxy, C3-C7 cycloalkyl, oxo, —OH, —NH2, CN and C1-C3 perfluoroalkyl; R2 is selected from H and halo; each R3 and R4 is independently selected from the group consisting of H, C1-C8 alkyl, —CN, halo, —OH, —O—(C1-C6 alkyl), —O—(C1-C6 alkyl)-O—(C1-C6 alkyl), —NR31R32, C1-C3 perfluoro alkyl, —O—(CH2)aNR31R32, —NR31—(CH2)aNR33R34, —NR31—(CH2)aOR33, aryl, C3-C7 cycloalkyl, a three to twelve membered heterocyclic ring having up to 3 heteroatoms which is optionally substituted from 1 to 3 substituents independently selected from halo, C1-C6 alkyl, and —(C1-C6 alkyl)-O—(C1-C6 alkyl); R31 and R32 are independently selected from the group consisting of H, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, and —(C1-C6 alkyl)-O—(C1-C6 alkyl); or R31 and R32 may be taken together to form a three to twelve membered heterocyclic ring having up to 3 heteroatoms which is optionally substituted from 1 to 3 substituents independently selected from halo and C1-C6 alkyl; R33 and R34 are independently selected from the group consisting of H and C1-C8 alkyl;a is selected from 0 to 6; R5 is selected from H and C1-C6 alkyl; R6 is selected from the group consisting of H, halo, and C1-C6 alkyl.
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