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One-pot synthesis of 5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one derivatives

机译:一锅合成5H-1,3,4-噻二唑并[3,2-a]嘧啶-5-酮衍生物

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摘要

A novel and efficient one-pot method has been developed for the synthesis of 2-substituted-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one derivative by the combination of [3 + 3] cycloaddition, reduction, deamination reactions. The fused heterocyclic compounds 2-substituted-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-ones was synthesized by the diversity-oriented catalysis. As an extension of the synthetic methodology, some 4H-pyrido[1,2-a]pyrimidin-4-one 4a-c was synthesized. The pi-pi accumulation structure of supramolecular self-assembly was discussed in the crystal.
机译:通过[3 + 3]的组合,开发了一种新颖且有效的一锅法,用于合成2-取代的-5H-1,3,4-噻二唑并[3,2-a]嘧啶-5-酮衍生物。环加成,还原,脱氨基反应。通过多样性取向催化合成了稠合的杂环化合物2-取代的-5H-1,3,4-噻二唑并[3,2-a]嘧啶-5-酮。作为合成方法的扩展,合成了一些4H-吡啶并[1,2-a]嘧啶-4-一4a-c。在晶体中讨论了超分子自组装的pi-pi积累结构。

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