Synthesis and antimicrobial screening of some new N3-substituted derivatives of quinazolin-4(3H)one

ABSTRACT:
Quinazolin-4-one-3-yl-propan-2-one (2) was prepared by N-alkylation of Quinazolin-4(3H)one 1. The treatment of compound 2 with hydrazine hydrate yielded hydrazine derivative (3), which on condensation with variously substituted aryl aldehydes gave the corresponding hydrazones (4). Compound 3 on reaction with phenyl isocyanate and phenyl isothiocyanate transformed into the corresponding carbamates and thiocarbamates (5) respectively. Compound 3 also gave a tricyclic compound (6) when refluxed in presence of ammonium acetate and acetic acid, while hydrazone derivative (7) when treated with dehydroacetic acid. Keywords: Quinazoline, chloroacetone, hydrazones.



For more details PDF Link: http://www.jocpr.com/articles/synthesis-and-antimicrobial-screening-of-some-new-n3substituted-derivatives-of-quinazolin43hone.pdf

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