The three-component reaction of 5-aminotetrazole with aliphatic aldehydes (formaldehyde, acetaldehyde) and acetoacetic ester derivatives in water under microwave irradiation leads to the selective formation of 4,7-dihydrotetrazolo[1,5-a]pyrimidine derivatives. Under similar conditions using 4,4,4-trifluoroacetoacetic ester 5-hydroxy-4,5,6,7-tetrahydrotetrazolo[1,5-a]pyrimidines are obtained. The analogous reaction with acetylacetone requires scandium(III) triflate as catalyst. The antioxidant activity of selected compounds was assayed with 1,1-diphenyl-2-picrylhydrazyl.
CITATION STYLE
Tkachenko, I. G., Komykhov, S. A., Musatov1, V. I., Shishkina, S. V., Dyakonenko, V. V., Shvets, V. N., … Desenko, S. M. (2019). In water multicomponent synthesis of low-molecular-mass 4,7-dihydrotetrazolo[1,5-a]pyrimidines. Beilstein Journal of Organic Chemistry, 15, 2390–2397. https://doi.org/10.3762/bjoc.15.231
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