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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 Full article

Journal Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436
Output data Year: 2009, Volume: 19, Number: 2, Pages: 87-88 Pages count : 2 DOI: 10.1016/j.mencom.2009.03.011
Authors Dudinov Arkady A. 1 , Lichitsky Boris V. 1 , Komogortsev Andrey N. 1 , Krayushkin Mikhail M. 1
Affiliations
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 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.
Cite: Dudinov A.A. , Lichitsky B.V. , Komogortsev A.N. , Krayushkin M.M.
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 Communications. 2009. V.19. N2. P.87-88. DOI: 10.1016/j.mencom.2009.03.011 WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:000265870700011
Scopus: 2-s2.0-63749105891
OpenAlex: W2951833383
Citing:
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OpenAlex 15
Scopus 15
Web of science 14
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