发明名称 BICYCLIC AZA COMPOUNDS AS MUSCARINIC M1 RECEPTOR AND/OR M4 RECEPTOR AGONISTS
摘要 This invention relates to compounds that are agonists of the muscarinic M1 receptor and/or M4 receptor and which are useful in the treatment of muscarinic M1/M4 receptor mediated diseases. Also provided are pharmaceutical compositions containing the compounds and the therapeutic uses of the compounds. Compounds include those according to formula (1), or a salt thereof, wherein Q, R1, R2, R3 and R4 are as defined herein.;
申请公布号 US2017015650(A1) 申请公布日期 2017.01.19
申请号 US201515117018 申请日期 2015.02.06
申请人 HEPTARES THERAPEUTICS LIMITED 发明人 Brown Giles Albert;Cansfield Julie Elaine;Congreve Miles Stuart;O'Brien Michael Alistair;Pickworth Mark;Rackham Mark David;Tehan Benjamin Gerald;Teobold Barry John
分类号 C07D401/14;C07D409/14;C07D405/14;C07D413/14;C07D417/14 主分类号 C07D401/14
代理机构 代理人
主权项 1. A compound of the formula (1b): or a salt thereof, wherein Q is an optionally substituted five or six or seven membered heterocyclic ring containing 1, 2, 3 or 4 heteroatom ring members selected from N, O and S; R3 is selected from hydrogen; fluorine; cyano; hydroxy; amino; and a C1-9 non-aromatic hydrocarbon group which is optionally substituted with one to six fluorine atoms and wherein one, two or three, but not all, carbon atoms of the hydrocarbon group may optionally be replaced by a heteroatom selected from O, N and S and oxidized forms thereof; R4 is a hydrogen or a C1-6 non-aromatic hydrocarbon group which is optionally substituted with one to six fluorine atoms and wherein one or two, but not all, carbon atoms of the hydrocarbon group may optionally be replaced by a heteroatom selected from O, N and S and oxidised forms thereof; and the dotted line indicates an optional second carbon-carbon bond, provided that when a second carbon-carbon bond is present, then R3 is absent.
地址 Welwyn Garden City, Hertfordshire GB