Abstract
A novel series of 2-alkoxy(aralkoxy)-4H-[1,2,4]triazolo[1,5-a]quinazolines were synthesized employing N-cyanoimidocarbonates and 2-hydrazinobenzoic acid as building blocks. Chemical transformation of the inherent lactam moiety in the targeted 2-alkoxy(aralkoxy)[1,2,4] triazolo[1,5-a] quinazolines was offered access to a variety of derivatives.