Synthesis, Antimicrobial, and Anti-HIV1 Activity of Quinazoline-4(3H)‎-one Derivatives

Joint Authors

Vijayakumar, K.
Thiruneelakandan, G.
Ahamed, A. Jafar

Source

Journal of Applied Chemistry

Issue

Vol. 2013, Issue 2013 (31 Dec. 2013), pp.1-5, 5 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2013-09-12

Country of Publication

Egypt

No. of Pages

5

Main Subjects

Engineering Sciences and Information Technology
Chemistry
Science

Abstract EN

The present investigation aims to synthesize 11 compounds of quinazoline-1 derivatives and to test their antimicrobial and anti-HIV1 activities.

A quick-witted method was developed for the synthesis of novel substituted quinazolinone derivatives by summarizing diverse diamines with benzoxazine reactions, and it demonstrated the benefits of typical reactions, handy operation, and outstanding product yields.

These compounds were confirmed by elemental analysis, I R, 1H NMR, 13C NMR, and mass spectra.

Then antimicrobial and anti-HIV1 activities of the compounds were tested in-vitro.

It was found that compounds 7–11 possessed a wide range of anti microbial and anti-HIV1 activity.

American Psychological Association (APA)

Vijayakumar, K.& Ahamed, A. Jafar& Thiruneelakandan, G.. 2013. Synthesis, Antimicrobial, and Anti-HIV1 Activity of Quinazoline-4(3H)-one Derivatives. Journal of Applied Chemistry،Vol. 2013, no. 2013, pp.1-5.
https://search.emarefa.net/detail/BIM-468121

Modern Language Association (MLA)

Vijayakumar, K.…[et al.]. Synthesis, Antimicrobial, and Anti-HIV1 Activity of Quinazoline-4(3H)-one Derivatives. Journal of Applied Chemistry No. 2013 (2013), pp.1-5.
https://search.emarefa.net/detail/BIM-468121

American Medical Association (AMA)

Vijayakumar, K.& Ahamed, A. Jafar& Thiruneelakandan, G.. Synthesis, Antimicrobial, and Anti-HIV1 Activity of Quinazoline-4(3H)-one Derivatives. Journal of Applied Chemistry. 2013. Vol. 2013, no. 2013, pp.1-5.
https://search.emarefa.net/detail/BIM-468121

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-468121