Synthesis and Antimicrobial Activity of Newer Quinazolinones
Author(s) -
Jayesh Patel,
B. D. Mistry,
K. R. Desai
Publication year - 2006
Publication title -
journal of chemistry
Language(s) - English
Resource type - Journals
eISSN - 2090-9063
pISSN - 2090-9071
DOI - 10.1155/2006/586512
Subject(s) - alkyl , benzaldehyde , chemistry , antimicrobial , methylene , aryl , medicinal chemistry , derivative (finance) , organic chemistry , catalysis , financial economics , economics
2–alkyl–6–bromo–3,1–benzoxazine–4–one (2) is synthesized by treating p–Bromoanthranilic acid and Acetylechoride or Benzoylchloride. Reaction of 2–alkyl–6–bromo–3,1–benzoxazine–4–one (2). with hydrazinehydrate furnish the corresponding 3–Amino–2–methyl–6–bromoquinazoline–4(3H)–one (3) which on reaction with benzaldehyde afford N,N – arylidene derivative (4). Reaction of 4 with various diazonium salts yields 6–bromo–2–alkyl/aryl–3{[phenyl(phenyldiazenyl)methylene]amino}quinazolin–4(3H)–one .
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