Polyfunctional imidazoles: XIV. 4-sulfonyl-5-formyl-1H-imidazoles
- 作者: Grozav A.N.1, Chornous V.A.1, Dorokhov V.I.2, Vovk M.V.2
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隶属关系:
- Bukovinian State Medical University
- Institute of Organic Chemistry
- 期: 卷 53, 编号 10 (2017)
- 页面: 1548-1555
- 栏目: Article
- URL: https://bakhtiniada.ru/1070-4280/article/view/216818
- DOI: https://doi.org/10.1134/S1070428017100104
- ID: 216818
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详细
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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