发明名称 Azabicyclohexanes
摘要 The present invention relates to novel compounds of Formula I, their pharmaceutically acceptable derivatives, tautomeric forms, stereoisomers including R and S isomers, polymorphs, prodrugs, metabolites, salts or solvates thereof. The invention also relates to processes for the synthesis of novel compounds of Formula I, their pharmaceutically acceptable derivatives, tautomeric forms, stereoisomers, polymorphs, prodrugs, metabolites, salts or solvates thereof.
申请公布号 US8906913(B2) 申请公布日期 2014.12.09
申请号 US201013380744 申请日期 2010.06.22
申请人 Panacea Biotec Limited 发明人 Jain Rajesh;Trehan Sanjay;Das Jagattaran;Kaur Gurmeet;Kanwar Sandeep;Singh Nishan;Nanda Gurmeet Kaur;Magadi Sitaram Kumar;Sharma Sudhir Kumar
分类号 A61K31/5355;C07D413/10;C07D209/52;C07D417/14;C07D491/08;C07D221/22;C07D487/04;C07D413/14;C07D409/04;C07D471/04;C07D417/10;C07D401/10 主分类号 A61K31/5355
代理机构 Lowe Hauptman & Ham, LLP 代理人 Lowe Hauptman & Ham, LLP
主权项 1. A compound of Formula Ib, or its tautomeric forms, stereoisomers including R and S isomers, or pharmaceutically acceptable salts thereof, wherein: ring A is phenyl; ring B is morphonilyl, attached to ring A through a nitrogen atom at any available position of ring A, ring B can further be fused to one or more aryl; R1, R2 and R4 are independently selected from —H, C1-12 alkyl, C2-12 alkenyl, C2-12 alkynyl, C1-12 alkoxyalkyl, C3-20 cycloalkyl, —CORa, —COORa, —CONRaRb, and —SO2Ra each of which may be optionally substituted at any available position by one or more substituents selected from but not limited to halogen, —ORa; R3 represents —(CH2)pZ; Z is selected from —H or —ORa; R5 is independently selected from —H, halogen; R6 is independently selected from —H or C1-12 alkyl; Q is O; Ra and Rb are same or different and can independently be selected from —H, C1-12 alkyl, C3-20 cycloalkyl, heterocyclyl, aryl, heteroaryl; m is 0, 1, 2, 3 or 4; r is 0, 1, 2, 3 or 4; p is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10; s is 0, 1, 2, 3 or 4.
地址 New Delhi IN