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One-pot synthesis of 135-triazine-24-dithione derivatives via three-component reactions

机译:通过三分组分反应的135-三嗪-24-二酮衍生物的单壶合成

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摘要

A catalyst-free one-pot synthetic methodology was developed for the preparation of 1,3,5-triazine-2,4-dithione derivatives through three-component reactions of arylaldehydes, thiourea, and orthoformates. The procedure tolerated a diverse range of arylaldehydes and orthoformates and provided a rapid entry to a variety of 4-aryl-6-(alkylthio)-3,4-dihydro-1,3,5-triazine-2(1H)-thiones (29 examples). The synthetic strategy relies on the dual role of thiourea in the cyclization with the aldehydes and the alkylation via an intermediate imidate formation. The structures of 1,3,5-triazine-2,4-dithione derivatives were characterized by spectroscopic techniques as well as by single crystal X-ray diffraction.
机译:开发出一种无催化剂的单罐合成方法,用于制备1,3,5-三嗪-2,4-二酮衍生物,通过芳族醛,硫脲和正畸的三分反应。该方法可容忍各种芳基醛和正交甲醛,并提供快速进入各种4-芳基-6-(烷硫基)-3,4-二氢-1,3,5-三嗪-2(1H) - 29例)。合成策略依赖于硫脲在用中间酰亚胺形成与醛和烷基化的环化中的双重作用。 1,3,5-三嗪-2,4-二酮衍生物的结构是通过光谱技术以及单晶X射线衍射的表征。

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