New spiro derivative of dihydro-1,2,3-triazolo[1,5-a]pyrimidine as a product of multicomponent reaction

11Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.
Get full text

Abstract

[Figure not available: see fulltext.] A new spiro derivative of dihydro-1,2,3-triazolo[1,5-a]pyrimidine – 5'-amino-6'-cyano-4'H-spiro[cyclohexane-1,7'-[1,2,3]triazolo[1,5-a]-pyrimidine]-3'-carboxamide – was prepared by three-component reaction of 5-amino-1,2,3-triazole-4-carboxamide with malononitrile and cyclohexanone; the structure of product was established by X-ray analysis. Microwave activation and conventional heating showed the formation of single product and the same direction of heterocyclization. Available literature data concerning similar reactions using 3-amino-1,2,4-triazole or 2-aminobenzimidazole were reinvestigated experimentally with consideration of alternative structures; structures of products were studied by NMR including NOE experiments.

Cite

CITATION STYLE

APA

Gladkov, E. S., Sirko, S. M., Musatov, V. I., Shishkina, S. V., Tkachenko, I. G., Komykhov, S. A., & Desenko, S. M. (2018). New spiro derivative of dihydro-1,2,3-triazolo[1,5-a]pyrimidine as a product of multicomponent reaction. Chemistry of Heterocyclic Compounds, 54(12), 1139–1144. https://doi.org/10.1007/s10593-019-02405-9

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free