首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >A short and convenient synthesis and evaluation of the antiinfective properties of indoloquinoline alkaloids: 10H-Indolo[3,2-b]quinoline and 7H-indolo[2,3-c]quinolines
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A short and convenient synthesis and evaluation of the antiinfective properties of indoloquinoline alkaloids: 10H-Indolo[3,2-b]quinoline and 7H-indolo[2,3-c]quinolines

机译:吲哚喹啉生物碱的简短合成及其抗感染性能的评价:10H-吲哚[3,2-b]喹啉和7H-吲哚[2,3-c]喹啉

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摘要

10H-Indolo[3,2-b]quinoline and 7H-indolo[2,3-c]quinoline have been synthesized in two steps using a modified approach to our previous reported method. Starting from commercially available 3-aminoquinoline and phenylboronic acid, the first step involved a copper acetate-catalyzed coupling reaction and the second utilized a palladium acetate-catalyzed intramolecular arylation reaction in the presence of trifluoroacetic acid as solvent. The anti-infective activity of a selected number of the compounds was also evaluated.
机译:10H-吲哚并[3,2-b]喹啉和7H-吲哚并[2,3-c]喹啉已通过两步合成,采用了我们先前报道的方法的改进方法。从可商购的3-氨基喹啉和苯基硼酸开始,第一步涉及乙酸铜催化的偶联反应,第二步在三氟乙酸作为溶剂的存在下利用乙酸钯催化的分子内芳基化反应。还评估了选定数量的化合物的抗感染活性。

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