首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Photochemical cyclization of thioformanilides by chloranil: An approach to 2-substituted benzothiazoles
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Photochemical cyclization of thioformanilides by chloranil: An approach to 2-substituted benzothiazoles

机译:苯甲酰氯对硫代甲酰苯胺的光化学环化:2-取代的苯并噻唑的制备方法

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摘要

2-Substituted benzothiazoles were efficiently synthesized by radical cyclization of thioformanilides induced by chloranil under irradiation in 1,2-dichloroethane and toluene at 80°C. Hydrogen atom abstraction from thiobenzamide by triplet chloranil was the key step of the mechanism, as confirmed by LFP experiments. The methodology developed is simple and afforded the easily isolated products from moderate to good yield.
机译:在1,2-二氯乙烷和甲苯中于80°C照射下,通过邻苯二甲酰氯诱导的硫代甲酰苯胺的自由基环化反应,可以高效地合成2-取代的苯并噻唑。 LFP实验证实,三重态氯苯腈从硫代苯甲酰胺中提取氢原子是该机理的关键步骤。所开发的方法很简单,并提供了容易分离的产物,产率从中等到良好。

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