SYTHESIS OF SOME 6-BROMO QUIAZOLIOE DERIVATIVES FOR THEIR PHARAMCOLOGICAL ACTIVITIES.

Authors

  • CH.RAJVEER Department of Pharmaceutical chemistry, Vaagdevi College of Pharmacy, Warangal.Andhrapradesh
  • D.KUMARASWAMY
  • S.SUDHARSHINI Department of Pharmaceutical chemistry, Vaagdevi College of Pharmacy, Warangal.Andhrapradesh
  • B.STEPHEN RATHINRAJ Department of Pharmaceutical chemistry, Vaagdevi College of Pharmacy, Warangal.Andhrapradesh.

Keywords:

Oxoquinazoline, Anti-inflammatory activity, Analgesic and Anti-bacterial activity.

Abstract

A number of substituted 6-bromoquinazolinones are known for their pharmacological importance like
anti-inflammatory, analgesic and anti-bacterial activity. In the present investigation is carried out for the
synthesis of 2-(6-bromo-2-phenyl-4-oxoquinazolin-3(4H)-yl)-N-substituted acetamides and 1-Amino-5-(6-
bromo-3, 4-dihydro-2-phenyl-4-oxoquinazolin-3yl) methyl-1, 3, 4-triazin-2-thiol to carry out their
pharmacological activities. A number of oxoquinazoline derivatives have been synthesized, purified and
characterized with the help of their analytical and spectral data (IR, NMR & Mass).The required ethyl [6-bromo-
2-phenyl-4-oxoquinazolin-3(4H)-yl] acetate has been synthesized from 6-bromo-2-phenyl-1,3,4-benzoxazinone
and ethyl glycinate. By the use of corresponding primary amines the N-substituted acetamides and by the use of
hydrazine hydrate the 1-amino-5-[6-bromo-2-phenyl-4-oxoquinazolin-3(4H)-yl] methyl 1, 3, 4-triazin-2-thiol
were prepared. The synthesized compounds were screened for their anti-bacterial activity, anti-inflammatory
activity and analgesic activity by standard methods. The compound shows Pharmacological activities in
comparison with the standard.

Published

30.09.2010

How to Cite

CH.RAJVEER, D.KUMARASWAMY, S.SUDHARSHINI, & B.STEPHEN RATHINRAJ. (2010). SYTHESIS OF SOME 6-BROMO QUIAZOLIOE DERIVATIVES FOR THEIR PHARAMCOLOGICAL ACTIVITIES. International Journal of Pharma and Bio Sciences, 1(3), 1–10. Retrieved from https://ijpbs.net/index.php/journal/article/view/264

Issue

Section

Research Articles