发明名称 Antibacterial compounds
摘要 The present invention relates to the following compounds for use in the treatment of a bacterial infection; wherein the integers are as defined in the description. The invention also relates to compounds for use as medicaments, pharmaceutical compositions and some novel compounds.
申请公布号 US9428474(B2) 申请公布日期 2016.08.30
申请号 US201314654186 申请日期 2013.12.20
申请人 Janssen Sciences Ireland UC 发明人 Guillemont Jérôme Émile Georges;Motte Magali Madeleine Simone;Koul Anil;Lounis Nacer
分类号 C07D263/58;C07D277/82;C07D277/62;A61K31/423;A61K31/428;A61K45/06 主分类号 C07D263/58
代理机构 代理人
主权项 1. A compound of formula (I): wherein R1, R2, R3 and R4 each independently are selected from the group consisting of: hydrogen, halo, —CN, Rt1, —O—Rt2, —C(O)N(Rt3)(Rt4), —SO2Rt5, —N(H)SO2Rt6, —N(Rt7)(Rt8), aryl and heterocyclic group wherein said aryl and said heterocyclic group optionally substituted by one or more substituents selected from halo and C1-6 alkyl; Rt1, Rt2, Rt3, Rt4, Rt5, Rt6, Rt7 and Rt8 independently are hydrogen or C1-6 alkyl wherein said C1-6 alkyl is optionally substituted by one or more halo atoms, or, Rt3 and Rt4 and/or Rt7 and Rt8 may be linked together with the nitrogen atom to which they are attached to form a 3- to 7-membered ring, optionally containing one to three additional heteroatoms and optionally contain one to three double bonds; Zx is O or S; X is S or O; ring A is either: Rx is hydrogen or C1-6 alkyl wherein said C1-6 alkyl is optionally substituted by one or more substituents selected from the group consisting of fluoro, —CN, —ORx1, and —C(O)Rx2; Rx1 and Rx2 independently are hydrogen or C1-6 alkyl; Ry3 independently is hydrogen, halo, C1-6 alkyl, —ORy4, —C(O)—Ry5 or —CH2—ORy6; Ry4, Ry5 and Ry6 independently are hydrogen or C1-6 alkyl; wherein Ry1 is fluoro, chloro, C1-6 alkyl, —OH, —C(O)Ry5 or —CH2—ORy6; and Ry2 is —OH, C1-6 alkyl, —C(O)Ry5 or —CH2—ORy6 or a pharmaceutically acceptable salt thereof.
地址 Little Island, Co Cork IE