Khanum, Shaukath Ara and Shashikanth, Sheena and Umesha, S. and Kavitha, R. (2005) Synthesis and antimicrobial study of novel heterocyclic compounds from hydroxybenzophenones. European Journal of Medicinal Chemistry, 40 (11). 1156 - 1162. ISSN 1768-3254
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Abstract
The triazolothiadiazine analogues 6a–e were obtained via a multistep synthesis sequences beginning with the hydroxybenzophenones 1a–e. Hydroxybenzophenones on reaction with ethyl chloroacetate affords ethyl (2-aroylaryloxy)acetates 2a–e which on treatment with hydrazine hydrate yields 2-(2-aroylaryloxy)acetohydrazides 3a–e. Intramolecular cyclization of 3a–e with carbon disulfide affords 5-(2-aroylaryloxy)methyl-1,3,4-oxadiazole-2-(3H)thiones 4a–e, which on treatment with hydrazine hydrate yields 4-amino-5-(2-aroyl aryloxy)methyl-1,2,4-triazole-3-(2H)thiones 5a–e. Condensation of 5a–e with α-halocarbonyl compound results in 3-(2-aroylaryloxy)methyl-6-phenyl-1,2,4-triazolo3,4-b1,3,4 thiadiazine 6a–e analogues. The compounds 4a–e, 5a–e and 6a–e were tested against variety of fungal and bacterial strains in comparison to fluconazole and chloramphenicol, respectively.
Item Type: | Article |
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Uncontrolled Keywords: | 1,3,4-Oxadiazole-2-(3H)thiones, 1,2,4-Triazole-3-(2H)thiones, 1,2,4-Triazolo thiadiazines, Synthesis, Antimicrobial activity |
Subjects: | C Chemical Science > Chemistry |
Divisions: | Yuvaraj college > Chemistry |
Depositing User: | Manjula P Library Assistant |
Date Deposited: | 04 Sep 2019 10:03 |
Last Modified: | 19 Dec 2020 06:13 |
URI: | http://eprints.uni-mysore.ac.in/id/eprint/7548 |
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