Synthesis and antimicrobial evaluation of imidazo-[1’,5’:1,2]pyrimido[4,5-d]isoxazolo[2,3-a]pyrimidin-10-ones
DOI:
https://doi.org/10.56042/ijc.v62i12.5927Keywords:
3-Amino-5-methyl-7-aryl-7H-isoxazolo[2,3-a]pyrimidin-6-yl cyanides, one-pot synthesis, Dimorth rearrangement, imidazo pyrimidoisoxazolo pyrimidines, Anti-microbial activityAbstract
A new series of novel imidazo-[1’,5’:1,2]pyrimido[4,5-d]isoxazolo[2,3-a]pyrimidin-10-ones (5) would be accomplished by reaction of 3-amino-5-methyl-7aryl-7H-isoxazolo[2,3-a]pyrimidin-6-yl cyanides (2),with choloacetylchloride followed by treatment with aromatic primary amines and, then with formaldehyde. The key intermediate (2), was obtained by reaction of 3-amino-5-methylisoxazole (1) with aromatic aldehydes, and malononitrile by a three-component one-pot synthesis. The structures of newly synthesized compounds (2-5) were established on the basis of spectral data, and evaluated for their in vitro antimicrobial activity.