Synthesis of some substituted pyrimidines via cycloaddition reaction of amidines and chalcones

Section: Article
Published
Jun 1, 2009
Pages
38-46

Abstract

ABSTRACT Substituted amidines (1,2) where prepared from the condensation of benzyl, furfuryl alcohols and ethyl sulphate with thiourea. Chalcone compounds (3,5a and 5b) where also prepared from condensation of 4-nitrobenzaldehyde to give compound (3) while acetophenone, 4-hydroxy benzaldehyde and 1,3-dibromopropane gave the diformyl intermediate (4) then it was underwent further reaction with either acetophenone or 4-methyl acetophenone to afford compounds (5a,5b) respectively. Condensation of the above amidines with the resulted chalcones or dichalcones afforded the substituted pyrimidines (6-11). Their structures confirmation were studied by IR and were discussed.

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How to Cite

[1]
H. M. Al-Ajely, هـ., G. T. Sedeek, غ., M. S. Al-Ajely, and م., “Synthesis of some substituted pyrimidines via cycloaddition reaction of amidines and chalcones”, EDUSJ, vol. 22, no. 2, pp. 38–46, Jun. 2009.