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通过自由基反应实现咪唑并[1,2-a]吡啶与醇的无金属位点特异性羟基烷基化反应

Metal-Free Site-Specific Hydroxyalkylation of Imidazo[1,2- a]pyridines with Alcohols through Radical Reaction.

作者信息

Jin Shengzhou, Xie Bo, Lin Sen, Min Cong, Deng Ruihong, Yan Zhaohua

机构信息

College of Chemistry , Nanchang University , Nanchang 330031 , P.R. China.

出版信息

Org Lett. 2019 May 3;21(9):3436-3440. doi: 10.1021/acs.orglett.9b01212. Epub 2019 Apr 17.

Abstract

An effective approach to realize the direct hydroxyalkylation of imidazo[1,2- a]pyridines with alcohols promoted by di- tert-butyl peroxide was described without any metal catalyst. It is the first time that the dehydrogenative C(sp)-C(sp) coupling of imidazo[1,2- a]pyridines with alcohols occurred regioselectively at the C-5 position of imidazo[1,2- a]pyridines. Multisubstituted imidazopyridine derivatives were smoothly synthesized in moderate to good yields. Through a series of control experiments, a free-radical pathway was proposed to explain the experiment.

摘要

描述了一种在无任何金属催化剂的情况下,通过二叔丁基过氧化物促进实现咪唑并[1,2-a]吡啶与醇的直接羟烷基化的有效方法。这是首次咪唑并[1,2-a]吡啶与醇的脱氢C(sp)-C(sp)偶联在咪唑并[1,2-a]吡啶的C-5位区域选择性地发生。多取代咪唑并吡啶衍生物以中等到良好的产率顺利合成。通过一系列对照实验,提出了一个自由基途径来解释该实验。

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