Synthesis of Some Functionalized Thiazolo[3,2-b][1,2,4]triazoles
Corresponding Author(s) : A. Davoodnia
adavoodnia@mshdiau.ac.ir
Asian Journal of Chemistry,
Vol. 23 No. 8 (2011): Vol 23 Issue 8
Abstract
A facile synthesis of some 6-aminothiazolo[3,2-b][1,2,4]triazole-5-carbonitriles in good yields has been developed through base catalyzed cyclocondensation of 1,2,4-triazole-3-thiones with bromomalononitrile. In case of phenyl derivative, hydrolysis of the cyano group into amide and subsequent cyclocondesation with benzoyl chloride afforded to the novel tricyclic compound 2,6-diphenyl[1,2,4]triazolo-[5',1':2,3][1,3]thiazolo[4,5-d]pyrimidin-8(7H)-one.
Keywords
1,2,4-Triazole-3-thiones
Thiazolo[3,2-b][1,2,4]triazoles
[1,2,4]Triazolo[5',1':2,3]- [1,3]thiazolo[4,5-d]pyrimidines
Bromomalononitrile
Davoodnia, A., Ameli, S., & Tavakoli-Hoseini, N. (2011). Synthesis of Some Functionalized Thiazolo[3,2-b][1,2,4]triazoles. Asian Journal of Chemistry, 23(8), 3707–3709. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/10674
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