Syntheses in the 4,5-dihydro-1,2,4-triazin-6-one-series

A study was carried out of alkylation, acylation and aminomethylation reactions were studied in the 5-alkyl-4,5-dihydro-1,2,4-triazin-4-one series. Alkylation by alkyl halides proceeds in the presence of sodium methylate at the N₍₁₎and N₍₄₎atoms with the formation of a mixture of alkylated compounds of three types: derivatives of 4,5-dihydrotriazine, unsaturated triazine, and their dimers. Acylation with isocyanates leads to the formation of heterocyclic ureas — derivatives at the N₍₄₎atom. Mono- and bisaminals were obtained by the reaction of triazines with ethoxymethyldiethylamine.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 963–970, July, 1991.