Visible-Light-Induced Regioselective C–H Sulfenylation of Pyrazolo[1,5-a]pyrimidines via Cross-Dehydrogenative Coupling

IF 3.6 2区 化学 Q1 CHEMISTRY, ORGANIC
Suvam Paul, Sourav Das, Tathagata Choudhuri, Papiya Sikdar and Avik Kumar Bagdi*, 
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引用次数: 0

Abstract

A visible-light-induced cross-dehydrogenative methodology has been developed for the regioselective sulfenylation of pyrazolo[1,5-a]pyrimidine derivatives. Rose bengal, blue LEDs, KI, K2S2O8, and DMSO are all essential for this photocatalytic transformation. The protocol is applicable for the synthesis of a library of 3-(aryl/heteroaryl thio)pyrazolo[1,5-a]pyrimidine derivatives with broad functionalities. The selectivity and scalability of the methodology have been also demonstrated. Moreover, the efficiency of this strategy for sulfenylation of pyrazoles, indole, imidazoheterocycles, and 4-hydroxy coumarin has been proven. The mechanistic investigation revealed the radical-based mechanism and formation of diaryl disulfide as a key intermediate for this cross-dehydrogenative coupling reaction.

Abstract Image

可见光诱导吡唑[1,5-a]嘧啶的区域选择性C-H磺化反应
一种可见光诱导的交叉脱氢方法用于吡唑[1,5- A]嘧啶衍生物的区域选择性磺化。红色孟加拉、蓝色led、KI、K2S2O8和DMSO都是这种光催化转化所必需的。该方案适用于合成具有广泛功能的3-(芳基/杂芳基硫代)吡唑[1,5-a]嘧啶衍生物库。该方法的选择性和可扩展性也得到了证明。此外,该策略在吡唑、吲哚、咪唑杂环和4-羟基香豆素的磺化反应中的效率已被证明。机理研究揭示了以自由基为基础的二芳基二硫醚的形成机理,二芳基二硫醚是交叉脱氢偶联反应的关键中间体。
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来源期刊
Journal of Organic Chemistry
Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
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