发明名称 Tricyclic antibiotics
摘要 The present invention relates to antibacterial compounds of formula I:; wherein all variable substituents are defined as described herein, which are useful for the treatment of bacterial infections.
申请公布号 US9321788(B2) 申请公布日期 2016.04.26
申请号 US201214124144 申请日期 2012.06.11
申请人 BASILEA PHARMACEUTICA AG 发明人 Gaucher Berangere;Danel Franck Hubert;Xie Tong;Xu Lin
分类号 C07D498/04;C07D491/14;C07D491/147;C07D491/052;C07D495/04 主分类号 C07D498/04
代理机构 代理人
主权项 1. A compound of formula I: wherein A1 represents —O—, —S— or —CH2—; A2 represents —CH2— or —O—; A3 represents C3-C8cycloalkylene; saturated or unsaturated 4 to 8-membered heterocyclodiyl with 1, 2 or 3 heteroatoms selected from nitrogen or oxygen, which group A3 is unsubstituted or substituted by one or more substituents each independently of the others being selected from fluorine, chlorine, bromine or iodine atoms, carboxy, alkyl, alkoxy, mono- or di(C1-C4alkyl)amino, OH, ═O, SH, ═S, NH2, ═NH, cyano, NO2, C1-C4alkoxycarbonyl, morpholinocarbonyl and hydroxyC1-C4alkyl groups; A4 represents C1-C4alkylene or —C(═O)—; G represents a group selected from pyrido[3,2-b][1,4]oxazine and benzo[1,4]oxazine which are unsubstituted or substituted by one or more substituents, each independently of the others being selected from fluorine, chlorine, bromine or iodine atoms, carboxy, alkyl, alkoxy, mono- or di(C1-C4alkyl)amino, OH, ═O, SH, ═S, NH2, ═NH cyano and NO2 groups and the pyrido or benzo part of the pyrido[3,2-b][1,4]oxazine and benzo[1,4]oxazine groups can also be substituted by C1-C4alkyl further substituted with fluoro; X1 represents a nitrogen atom or CR1; R1 represents a hydrogen atom or a halogen atom; R2 represents a hydrogen atom; m is 0 or 1; n is 1; the —(CH2)n— group is unsubstituted; p is 0 or 1; or a pharmaceutically acceptable salt thereof.
地址 Basel CH
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