

METHOD FOR THE SYNTHESIS OF CHROMENOPYRIMIDINE-FUSED AZOLES BY COPPER-CATALYZED INTRAMOLECULAR HETERO-DIELS–ALDER REACTION

Abstract
One-pot efficient copper-catalyzed approach for the synthesis of tetracyclic chromeno[4',3':4,5]pyrimido[1,2-b]indazolone and chromeno[4,3-d][1,2,4]triazolo[4,3-a]pyrimidine derivatives as a class of pharmacologically interesting compounds through the intramolecular domino condensation–aza-Diels–Alder reaction of aminoazoles and o-propargylated salicylaldehydes under reflux conditions has been described.
Keywords
aminoazole; chromenopyrimidine; copper catalyst; intramolecular hetero-Diels–Alder reaction.
Latvian Institute of Organic Synthesis - Aizkraukles iela, 21, Riga, LV-1006, Latvia - hgs@osi.lv