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Mendeleev Communications, 2009, Volume 19, Issue 2, Pages 87–88
DOI: https://doi.org/10.1016/j.mencom.2009.03.011
(Mi mendc3127)
 

This article is cited in 15 scientific papers (total in 15 papers)

Three-component condensation of 2,4-diaminothiazoles with aldehydes and Meldrum's acid: synthesis of 7-aryl(alkyl)-substituted 6,7-dihydro-4H-thiazolo[4,5-b]pyridin-5-ones

A. A. Dudinov, B. V. Lichitsky, A. N. Komogortsev, M. M. Krayushkin

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Abstract: The new method of the synthesis of 6,7-dihydro-4H-thiazolo[4,5-b]pyridin-5-ones, based on decarboxylation of corresponding 2,4-diamino-5-thiazolecarboxylic acids has been elaborated; unstable derivatives of 2,4-diaminothiazole, generated in situ as a result of decarboxylation, react with aldehydes and Meldrum's acid forming target compounds.
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Document Type: Article
Language: English


Citation: A. A. Dudinov, B. V. Lichitsky, A. N. Komogortsev, M. M. Krayushkin, “Three-component condensation of 2,4-diaminothiazoles with aldehydes and Meldrum's acid: synthesis of 7-aryl(alkyl)-substituted 6,7-dihydro-4H-thiazolo[4,5-b]pyridin-5-ones”, Mendeleev Commun., 19:2 (2009), 87–88
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  • https://www.mathnet.ru/eng/mendc/v19/i2/p87
  • This publication is cited in the following 15 articles:
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