发明名称 CERTAIN (2S)-N-[(1S)-1-CYANO-2-PHENYLETHYL]-1,4-OXAZEPANE-2-CARBOXAMIDES AS DIPEPTIDYL PEPTIDASE 1 INHIBITORS
摘要 The present disclosure relates to certain (2S)-N-[(1S)-1-cyano-2-phenylethyl]-1,4-oxazepane-2-carboxamide compounds (including pharmaceutically acceptable salts thereof),;;that inhibit dipeptidyl peptidase 1 (DPP1) activity, to their utility in treating and/or preventing clinical conditions including respiratory diseases, such as asthma and chronic obstructive pulmonary disease (COPD), to their use in therapy, to pharmaceutical compositions containing them and to processes for preparing such compounds.
申请公布号 US2017057938(A1) 申请公布日期 2017.03.02
申请号 US201615346411 申请日期 2016.11.08
申请人 AstraZeneca AB 发明人 LONN Hans Roland;CONNOLLY Stephen;SWALLOW Steven;KARLSSON Staffan PO;AURELL Carl-Johan;PONTÉN John Fritiof;DOYLE Kevin James;VAN DE POËL Amanda Jane;JONES Graham Peter;WATSON David Wyn;MACRITCHIE Jaqueline Anne;PALMER Nicholas John
分类号 C07D267/10;C07D413/14;C07D413/12;C07D417/12;A61K45/06;A61K31/553 主分类号 C07D267/10
代理机构 代理人
主权项 1. A compound of formula (I)wherein R1 is R2 is selected from hydrogen, F, Cl, Br, OSO2C1-3alkyl, or C1-3alkyl; R3 is selected from hydrogen, F, Cl, Br, CN, CF3, SO2C1-3alkyl, CONH2 or SO2NR4R5, wherein R4 and R5 together with the nitrogen atom to which they are attached form a azetidine, pyrrolidine or piperidine ring; orR1 is selected from X is selected from O, S or CF2; Y is selected from O or S; Q is selected from CH or N; R6 is selected from C1-3alkyl, wherein said C1-3alkyl is optionally substituted by 1, 2 or 3 F and optionally by one substituent selected from OH, OC1-3alkyl, N(C1-3alkyl)2, cyclopropyl, or tetrapydropyran; R7 is selected from hydrogen, F, Cl or CH3; or a pharmaceutically-acceptable salt thereof.
地址 Sodertalje SE