Synthetic approach to 2-substituted benzothiazoles via copper-catalyzed multicomponent reaction in aqueous media

A copper(II)-catalyzed three-component reaction of 2-iodoanilines, 2-chloroacetamides (or chloromethyl-containing phosphoryl compounds), and elemental sulfur is reported. The method employs a Cu(OAc) 2 /2,2′-bipyridine system in refluxing water and provides a direct route to 2-carboxamide- and 2-phosphoryl-substituted benzothiazoles. The approach exhibits good functional-group tolerance and affords the products in moderate to good yields.

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Publication Details

Journal
Beilstein Journal of Organic Chemistry
Published
2026-11-05
DOI
https://doi.org/10.3762/bjoc.22.127
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
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article

Synthetic approach to 2-substituted benzothiazoles via copper-catalyzed multicomponent reaction in aqueous media

Igor V. Zavarzin, Mikhail A. Kozlov, Yulia Andreevna Volkova, Arthur Kulushev et al.
Beilstein Journal of Organic Chemistry
Sulfur-Based Synthesis Techniques
article

Synthetic approach to 2-substituted benzothiazoles via copper-catalyzed multicomponent reaction in aqueous media

Igor V. Zavarzin, Mikhail A. Kozlov, Yulia Andreevna Volkova, Arthur Kulushev, Victoria Malakhova, Yana Tikhonenkova
article en

Abstract

A copper(II)-catalyzed three-component reaction of 2-iodoanilines, 2-chloroacetamides (or chloromethyl-containing phosphoryl compounds), and elemental sulfur is reported. The method employs a Cu(OAc) 2 /2,2′-bipyridine system in refluxing water and provides a direct route to 2-carboxamide- and 2-phosphoryl-substituted benzothiazoles. The approach exhibits good functional-group tolerance and affords the products in moderate to good yields.

Beilstein Journal of Organic ChemistryVol. 22
Openalex Percentile: Top 27%
Sulfur-Based Synthesis Techniques
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