

EFFECTIVE METHOD FOR THE SYNTHESIS OF AZOLO[1,5-a]PYRIMIDIN-7-AMINES

Abstract
Condensation of aminoazoles with (2E)-(3-morpholin-4-yl)acrylonitrile and 3,3-diethoxypropionitrile was used to synthesize a series of azolo[1,5-a]pyrimidin-7-amines. It was established that the reactions with certain aminotriazoles gave mixtures of regioisomers: azolo[1,5-а]pyrimidin-7-amines and azolo[4,3-а]pyrimidin-5-amines.
Keywords
azolo[1,5-a]pyrimidin-7-amines; 3,3-diethoxypropionitrile; (2E)-(3-morpholin-4-yl)acrylonitrile; Dimroth rearrangement; heterocyclization
Latvian Institute of Organic Synthesis - Aizkraukles iela, 21, Riga, LV-1006, Latvia - hgs@osi.lv