IONIC LIQUID-MEDIATED FACILE SYNTHESIS AND ANTIMICROBIAL STUDY OF THIAZOLO [2,3-b]BENZO[h]QUINAZOLINES AND THIAZINO[2,3-b] BENZO-[h]QUINAZOLINES

Gupta, R; Chaudhary, R

HERO ID

5424781

Reference Type

Journal Article

Year

2012

Language

English

HERO ID 5424781
In Press No
Year 2012
Title IONIC LIQUID-MEDIATED FACILE SYNTHESIS AND ANTIMICROBIAL STUDY OF THIAZOLO [2,3-b]BENZO[h]QUINAZOLINES AND THIAZINO[2,3-b] BENZO-[h]QUINAZOLINES
Authors Gupta, R; Chaudhary, R
Journal Phosphorus, Sulfur, and Silicon and the Related Elements
Volume 187
Issue 6
Page Numbers 735-742
Abstract 8-Methoxy-4-phenyl-3,4,5,6-tetrahydrobenzo[h]quinazoline-2(1H)-thi one, obtained by the condensation of 2-benzylidene-6-methoxy-3,4-dihydronapthalene-1(2H)-one with thiourea, on reaction with chloroacetic acid and 3-chloropropanoic acid in the presence of the ionic liquid N-methylpyridinium tosylate furnishes 3-methoxy-7-phenyl-7,10-dihydro-5H- benzo[h]thiazolo[2,3-b]quinazoline-9(6H)-one and 3-methoxy-7-phenyl-5,6,10,11-tetrahydro- benzo[h][1,3]thiazino[2,3-b]quinazoline-9(7H)-one. Further, condensation of the thione with 1,2-dibromoethane and 1,3-dibromopropane yields 3-methoxy-7-phenyl-6,7,9,10-tetrahydro-5 H-benzo[h]thiazolo[2,3-b]quinazoline and 3-methoxy-7-phenyl-5,6,7,9,10,11-hexahydrobenzo [h][1,3]thiazino[2,3-b]quinazoline respectively. Arylidene derivatives have been obtained by two routes. The structures of the cyclized compounds have been established on the basis of elemental analysis and spectroscopic data. The synthesized compounds were screened for antimicrobial activity. Some of the compounds showed promising antimicrobial activities.
Doi 10.1080/10426507.2011.647145
Wosid WOS:000304271300008
Url https://search.proquest.com/docview/1758240414?accountid=171501
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English
Keyword Ionic liquid; 4-thiazolidinone; antimicrobial activity; arylidene derivatives