Alkylation of 4-anilino-5-phenyl-4H-1,2,4-triazole-3-thiol (1) with some halo compounds yielded the corresponding sulfides 2a–f. Some sulfides 2e,f were cyclized to give triazolothiadiazines 3 and 4. Triazolothiadiazoles 5 and 6 were prepared through the reaction of compound 1 with carbon disulfide or ethyl orthoformate, respectively. Treatment of compound 1 with ethyl chloroformate or phenyl isothiocyanate yielded triazolo-thiadiazole and triazole 9 and 10, ... إقراء المزيد

Reaction of 5-aryl-3-chloro-4-phenyl-1,2,4-triazoles (1 & 2) with hydrazine hydrate afforded the hydrazino derivatives 3 and 4. Reaction of 3 and 4 with carboxylic acids, CS2 and phenylisothiocyanate gave the s-triazole-fused ring systems 5–12. On the other hand, reaction of 3 and 4 with nitrous acid gave tetrazole-fused ring systems 13 and 14, respectively. Mannich reaction on compounds 9 and 10 ... إقراء المزيد