Polyfunctional imidazoles: XIV. 4-sulfonyl-5-formyl-1H-imidazoles


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Oxidative chlorination of 1-aryl-4-benzylsulfanyl-1H-imidazole-5-carbaldehydes gave 1-aryl-5-formyl-1H-imidazole-4-sulfonyl chlorides which reacted with secondary amines and phenols to produce the corresponding N,N-disubstituted 5-formylimidazole-4-sulfonamides and aryl sulfonates. The reaction of 1-aryl-5-formyl-1H-imidazole-4-sulfonyl chlorides with sodium azide, followed by reduction of the resulting sulfonyl azides, led to the formation of N-unsubstituted 5-formylimidazole-4-sulfonamides, and the reaction with alcohols, to 5-formylimidazole-4-sulfonic acids.

作者简介

A. Grozav

Bukovinian State Medical University

编辑信件的主要联系方式.
Email: alinagrozav@gmail.com
乌克兰, Teatral’naya pl. 2, Chernovtsy, 58000

V. Chornous

Bukovinian State Medical University

Email: alinagrozav@gmail.com
乌克兰, Teatral’naya pl. 2, Chernovtsy, 58000

V. Dorokhov

Institute of Organic Chemistry

Email: alinagrozav@gmail.com
乌克兰, ul. Murmanskaya 5, Kiev, 02660

M. Vovk

Institute of Organic Chemistry

Email: alinagrozav@gmail.com
乌克兰, ul. Murmanskaya 5, Kiev, 02660

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