Imidazol-2-yl derivatives of substituted bicyclic compounds
    63.
    发明授权
    Imidazol-2-yl derivatives of substituted bicyclic compounds 失效
    取代的双环化合物的咪唑-2-基衍生物

    公开(公告)号:US5356920A

    公开(公告)日:1994-10-18

    申请号:US915835

    申请日:1992-07-24

    CPC分类号: C07D233/64 C07D405/04

    摘要: Compounds having formula (I) ##STR1## wherein Z is --O-- or --CH.sub.2 --; n is 1-6; R is hydrogen, C.sub.1 -C.sub.6 alkyl, phenyl or optionally substituted phenyl-C.sub.1 -C.sub.3 alkyl; R.sub.2 is C.sub.1 -C.sub.8 -alkyl, aryl-C.sub.1 -C.sub.3 alkyl, C.sub.5 -C.sub.8 cycloalkyl or C.sub.5 -C.sub.8 cycloalkyl-C.sub.1 -C.sub.3 alkyl; each of R.sub.3 and R.sub.4 independently is hydrogen or C.sub.1 -C.sub.4 alkyl, or taken together with the carbon atom to which they are linked form a C.sub.3 -C.sub.6 cycloalkyl ring; Q is --OR' or --NR'R" in which R' and R" are as herein defined, or Q is C.sub.1 -C.sub.8 alkyl, phenyl, phenyl-C.sub.1 -C.sub.3 -alkyl, C.sub.5 -C.sub.8 cycloalkyl or C.sub.5 -C.sub.8 cycloalkyl-C.sub.1 -C.sub.3 alkyl, in which both the phenyl and cycloalkyl rings or moieties are optionally substituted as herein defined; and the pharmaceutically acceptable salts thereof; are useful in particular as antidislipidaemic and antiatherosclerotic agents.

    摘要翻译: PCT No.PCT / EP91 / 02228 371日期:1992年7月24日 102(e)日期1992年7月24日PCT 1991年11月26日PCT公布。 出版物WO89 / 08646 日本9月21日,1989。具有式(I)的化合物其中Z为-O-或-CH 2 - ; n为1-6; R是氢,C 1 -C 6烷基,苯基或任选取代的苯基-C 1 -C 3烷基; R 2是C 1 -C 8 - 烷基,芳基-C 1 -C 3烷基,C 5 -C 8环烷基或C 5 -C 8环烷基-C 1 -C 3烷基; R 3和R 4各自独立地为氢或C 1 -C 4烷基,或与它们所连接的碳原子一起形成C 3 -C 6环烷基环; Q是-OR'或-NR'R“,其中R'和R”如本文所定义,或Q是C1-C8烷基,苯基,苯基-C1-C3-烷基,C5-C8环烷基或C5- C8环烷基-C1-C3烷基,其中苯基和环烷基环或任选被任意取代,如本文所定义; 及其药学上可接受的盐; 特别是作为抗皮脂血症和抗动脉粥样硬化剂有用。