Imidazo [1,2-a] pyridines substituted with a thienyl, thiazolyl, or
thiadiazolyl group
    91.
    发明授权
    Imidazo [1,2-a] pyridines substituted with a thienyl, thiazolyl, or thiadiazolyl group 失效
    咪唑并[8,12-a {9 {0噻吩,噻唑基或噻二唑基取代的吡啶

    公开(公告)号:US4105767A

    公开(公告)日:1978-08-08

    申请号:US781902

    申请日:1977-03-28

    摘要: Certain novel substituted imidazo [1,2-a] pyridines with a substituted amino group at the 2- or 3- position and a heterocyclic moiety on the pyrido portion of the molecule are active anthelmintic agents. The heterocyclic moiety is connected to the imidazo [1,2-a] pyridine molecule through an oxygen, sulfur, sulfinyl or sulfone. The novel compounds are prepared from the appropriately substituted 2-amino pyridine precursor. Compositions which utilize said novel imidazo [1,2-a] pyridines as the active ingredient thereof for the treatment of helminthiasis are also disclosed.

    摘要翻译: 某些在2-或3-位具有取代氨基的取代咪唑并[1,2-a]吡啶和分子的吡啶部分上的杂环部分是活性的驱虫剂。 杂环部分通过氧,硫,亚磺酰基或砜与咪唑并[1,2-a]吡啶分子连接。 该新化合物由适当取代的2-氨基吡啶前体制备。 还公开了利用所述新型咪唑并[1,2-a]吡啶作为其活性成分用于治疗蠕虫病的组合物。