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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >SYNTHESIS OF 4-ARYLISOQUINOLINE-1(2H)-THIONE DERIVATIVES BY SODIUM HYDRIDE-MEDIATED CYCLIZATIONS OF 2-(1-ARYLETHENYL)BENZOTHIOAMIDES
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SYNTHESIS OF 4-ARYLISOQUINOLINE-1(2H)-THIONE DERIVATIVES BY SODIUM HYDRIDE-MEDIATED CYCLIZATIONS OF 2-(1-ARYLETHENYL)BENZOTHIOAMIDES

机译:通过氢化钠介导的2-(1-芳基乙基)苯并噻嗪的氢化钠介导的环戊衍生物合成4-芳基喹啉-1(2H) - 硫酮衍生物

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摘要

A new and facile method for the general preparation of isoquinoline-1(2H)-thione derivatives has been developed. Thus, the sodium hydride-mediated cyclization of N-substituted 2-(1-arylethenyl)benzothioamides, which are derived from the reaction of 2-(1-arylethenyl)phenyllithiums with isothiocyanates, gives 2-substituted 4-aryl-3,4-dihydroisoquinoline-1(2H)-thiones. In addition, the use of N-substituted 2-(1-aryl-2-methoxyethenyl)benzothioamides from 2-(1-aryl-2-methoxyethenyl)phenyllithiums and isothiocyanates affording 2-substituted 4-arylisoquinoline-1(2H)-thiones is described.
机译:已经开发出一种新的和容易制备异喹啉-1(2H) - 硫酮衍生物的方法。 因此,N-取代的2-(1-芳基乙烯基)苯并噻吩的氢化钠介导的环化,其衍生自2-(1-芳基乙基)苯基锂与异硫氰酸酯的反应,得到2取代的4-芳基-3,4 -dihydroisoquinoline-1(2h) - 第四次。 此外,使用N-取代的2-(1-芳基-2-甲氧基甲基苯基)苯并噻嗪,来自2-(1-芳基-2-甲氧基甲基)苯基锂和异硫氰酸酯,得到2-取代的4-芳基喹啉-1(2H) - 最活体 描述了。

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