A Facile Synthesis of 3-Substituted-2-styryl-4-quinazolones
Corresponding Author(s) : ARCHANA TAUNK
purbasha_3_1@yahoo.com
Asian Journal of Chemistry,
Vol. 21 No. 5 (2009): Vol 21 Issue 5
Abstract
2-Methyl-3,1-benzoxazine-4-one (3), generated by cyclizing of N-acetyl-anthranilic acid with ethyl chloroformate in benzene containing triethyl-amine, reacts with primary amine and subsequently aromatic aldehyde when heated under reflux in glacial acetic acid to give 3-substituted 2-styryl-3,4-dihydro-4-quinazolones (7).
Keywords
Synthesis
3-Substituted-2-styryl quinazolones
DASGUPTA, P., & TAUNK, A. (2010). A Facile Synthesis of 3-Substituted-2-styryl-4-quinazolones. Asian Journal of Chemistry, 21(5), 3535–3539. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/17327
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