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无金属条件下硫代酰胺的分子内脱氢 C-S 键偶联形成 1,3-苯并噻嗪。

Intramolecular dehydrogenative C-S bond coupling of thioamides to form 1,3-benzothiazines under metal-free conditions.

机构信息

State Key Laboratory Base of Eco-Chemical Engineering, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, P. R. China.

出版信息

Org Biomol Chem. 2019 Mar 27;17(13):3356-3360. doi: 10.1039/c9ob00237e.

Abstract

A novel HTIB-promoted direct intramolecular dehydrogenative C-S bond coupling reaction of thioamides has been developed to provide 1,3-benzothiazine derivatives in good yields. The reaction proceeds smoothly to reach completion at room temperature within 1 min under metal-free conditions. This protocol provides a mild and efficient strategy for the synthesis of six-membered N,S-containing heterocycles. Preliminary mechanistic studies indicate that a spirocyclic intermediate might be involved.

摘要

一种新型的 HTIB 促进的硫代酰胺的直接分子内脱氢 C-S 键偶联反应已经被开发出来,用于以良好的收率提供 1,3-苯并噻嗪衍生物。该反应在无金属条件下在室温下 1 分钟内即可顺利完成。该方案为六元 N,S 杂环化合物的合成提供了一种温和有效的策略。初步的机理研究表明,可能涉及螺环中间体。

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