在无金属条件下化学和区域选择性合成喹啉的C3磺酸盐和C4氯化物†

Dong Chen , Yan Liu , Zhiqiang Lu , Haojie Wang , Mingjia Li , Dan Yue , Zhenling Wang
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引用次数: 0

摘要

本文公开了一种由喹啉N-氧化物与磺酰氯一锅合成喹啉的C3磺酸酯和C4氯化物的新方法。磺酰氯有两种作用,即磺酰化作用和氯化作用。芳烃磺酰氯和脂肪族磺酰氯都是磺化和氯化试剂的合适前体。因此,在不含金属的条件下,得到了多种喹啉的C3磺酸盐和C4氯化物。该程序具有实用性、高效性、环境友好性和原子经济性等特点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Chemo- and regioselective synthesis of C3-sulfonate esters and C4-chlorides of quinolines under metal-free conditions†

Chemo- and regioselective synthesis of C3-sulfonate esters and C4-chlorides of quinolines under metal-free conditions†

Disclosed herein is a novel one-pot synthesis of C3-sulfonate esters and C4-chlorides of quinolines from quinoline N-oxides with sulfonyl chloride. Sulfonyl chlorides were used in two roles, namely sulfonylation and chlorination. Both arenesulfonyl chlorides and aliphatic sulfonyl chlorides were found to be suitable precursors for sulfonation and chlorination reagents. Therefore, a wide variety of C3-sulfonate esters and C4-chlorides of quinolines were afforded under metal-free conditions. This procedure features practicality, high efficiency, environmental friendliness and atomic economy.

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