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首页> 外文期刊>Russian Chemical Bulletin >Synthesis of 4-oxothiazolidine-2,5-diylidenes containing thioamide group based on dithiomalonamides
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Synthesis of 4-oxothiazolidine-2,5-diylidenes containing thioamide group based on dithiomalonamides

机译:基于二硫代丙二酰胺的含硫酰胺基的4-氧噻唑烷-2,5-二亚甲基的合成

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摘要

An approach to the synthesis of 2-(4-oxo-3-arylthiazolidine-2,5-diylidene)-N-arylethanethioamide derivatives from N,N'-diarylmalonodithioamides includes two steps: preparation of thiazoles using the Hantzsch reaction with subsequent modification of the active methylene group by the Knoevenagel condensation or enamination using dimethylformamide dimethyl acetal (DMF-DMA). Configuration and isomerization of the double bonds in 4-oxothiazolidine2,5-diylidenes were confirmed by H-1 NMR and X-ray diffraction analysis and discussed.
机译:由N,N′-二芳基丙二二硫代酰胺合成2-(4-氧代-3-芳基噻唑烷-2,5-二亚甲基)-N-芳基乙硫酰胺衍生物的方法包括两个步骤:使用汉茨反应制备噻唑,随后对其进行修饰。 Knoevenagel缩合或使用二甲基甲酰胺二甲基乙缩醛(DMF-DMA)引发的活性亚甲基通过H-1 NMR和X射线衍射分析确认并讨论了4-氧噻唑烷2,5-二亚甲基双键的构型和异构化。

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