5-(4,6-Diphenyl-2-pyrimidinyl)-1,3,4-oxadiazole-2-thione with Some C-Electrophiles and N-Nucleophiles.

Autor: Mekuskiene, G., Burbuliene, M. M., Jakubkiene, V., Udrenaite, E., Gaidelis, P., Vainilavicius, P.
Předmět:
Zdroj: Chemistry of Heterocyclic Compounds; Oct2003, Vol. 39 Issue 10, p1364-1368, 5p
Abstrakt: 5-(4,6-Diphenyl-2-pyrimidinyl)-1,3,4-oxadiazole-2-thione reacted with haloalkanes or their derivatives containing side chain oxo group to give S-alkylated compounds. Aminomethylation and acylation of the thione yielded N(3)-derivatives. Treatment of the title compound with hydrazine hydrate in butanol resulted in 4-amino-5-(4,6-diphenyl-2-pyrimidinyl)-1,2,4-triazole-3-thione via a recyclization reaction. Reaction of the title compound with hydrazine hydrate or phenylhydrazine in dioxane led to formation of the corresponding thiocarbohydrazides. The latter in the presence of a base were cyclized to 4-amino-1,2,4-triazole-3-thiones. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index