Modular multicomponent cascade synthesis of benzo[b]thiophene-fused N,O-heterocycles from 1,2-benzisothiazoles, benzolactones and aldehydes

Longzhi Lin, Jie Ren, Heying Chen, Shuang Liu, Chuanjun Song, Junbiao Chang, Yangang Wu
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引用次数: 0

Abstract

A modular, metal-free multicomponent cascade reaction for the synthesis of benzo[b]thiophene-fused seven- or eight-membered N,O-heterocyclic compounds from 1,2-benzisothiazoles, benzolactones, and aldehydes has been developed. Notably, 1,2-benzisothiazoles were employed as novel sulfuration reagents in multicomponent reactions for the first time. The regioselectivity of this modular transformation is controlled by the in situ ring-opening of 1,2-benzisothiazoles with benzolactones, a process involving N–S bond cleavage and decarboxylation. This modular multicomponent cascade reaction proceeds under mild conditions, exhibits broad substrate tolerance, and enables the one-step formation of new C–C, C–S, C–N, and C–O bonds. Moreover, the successful scale-up synthesis and efficient late-stage modification of pharmaceutical molecules highlight the synthetic utility of this method.
1,2-苯并异噻唑、苯并内酯和醛的模块化多组分级联合成苯并[b]噻吩- N, o杂环
以1,2-苯并异噻唑、苯并内酯和醛为原料,建立了一种模块化、无金属的多组分级联反应,用于合成苯并[b]噻吩-融合的七元或八元N, o杂环化合物。值得注意的是,1,2-苯并异噻唑首次在多组分反应中作为新型的硫化试剂。这种模块化转化的区域选择性由1,2-苯并异噻唑与苯并内酯的原位开环控制,这一过程涉及到N-S键的裂解和脱羧。这种模块化的多组分级联反应在温和的条件下进行,具有广泛的底物耐受性,并且能够一步形成新的C-C, C-S, C-N和C-O键。此外,成功的大规模合成和药物分子的高效后期修饰突出了该方法的合成实用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
7.80
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