3-Aryl-2(3)-halogenacrylates as Key Synthons in the Regioselective Synthesis of Two Types of Imidazothiazinotriazines

A method for the synthesis of two series of regioisomeric imidazothiazinotriazines was developed by cyclocondensation of imidazotriazinethiones with 3-aryl-2(3)-halogenacrylates or corresponding acrylonitriles. Regioselectivity of the process depended on the substituents at positions 4a and 7a of imidazotriazinethione. The reaction of 4a,7a-unsubstituted derivatives resulted in imidazo­[4,5-e]­[1,3]­thiazino­[2,3-c]­[1,2,4]­triazines of angular structure while the cyclocondensation of 4a,7a-diarylsubstituted compounds led to imidazo­[4,5-e]­[1,3]­thiazino­[3,2-b]­[1,2,4]­triazines of linear structure. The scope of the method was extended to benzimidazolethione that reacted with 3-aryl-2(3)-halogenacrylates or acrylonitriles to give benzo­[4,5]­imidazo­[2,1-b]­[1,3]­thiazines.