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首页> 外文期刊>Bioorganic and medicinal chemistry >C-C bond formation at C-2 of a quinoline ring: Synthesis of 2-(1H-indol-3-yl)quinoline-3-carbonitrile derivatives as a new class of PDE4 inhibitors
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C-C bond formation at C-2 of a quinoline ring: Synthesis of 2-(1H-indol-3-yl)quinoline-3-carbonitrile derivatives as a new class of PDE4 inhibitors

机译:在喹啉环的C-2处形成C-C键:合成2-(1H-吲哚-3-基)喹啉-3-甲腈衍生物作为一类新的PDE4抑制剂

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摘要

A number of 2-(1H-indol-3-yl)quinoline-3-carbonitrile derivatives were synthesized via AlCl 3-mediated C-C bond forming reaction between 2-chloroquinoline-3-carbonitrile and various indoles. The methodology does not require any N-protection of the indoles employed and provided the corresponding products in good yields. The molecular structure of a representative compound was established unambiguously by single crystal X-ray diffraction and structural elaboration of a compound synthesized has been demonstrated. Many of these compounds synthesized showed PDE4 inhibitory properties in vitro. A brief structure-activity relationship studies within the series along with docking results of a representative compound (EC 50 ~0.89 μM) is presented.
机译:通过2-氯喹啉-3-腈与各种吲哚之间的AlCl 3介导的C-C键形成反应,合成了许多2-(1H-吲哚-3-基)喹啉-3-腈衍生物。该方法不需要对所用的吲哚进行任何N-保护,并以高收率提供了相应的产物。通过单晶X射线衍射明确地确定了代表性化合物的分子结构,并且已经证明了合成化合物的结构精细化。这些合成的许多化合物在体外均表现出PDE4抑制特性。简要介绍了该系列化合物之间的结构-活性关系,以及代表性化合物(EC 50〜0.89μM)的对接结果。

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