Synthesis and antimicrobial evaluation of novel 1,3,4-thiadiazole derivatives of 2-(4-formyl-2-methoxyphenoxy) acetic acid

A series of 1,3,4-thiadiazole derivatives of 2-(4-formyl-2-methoxyphenoxy) acetic acid (6a–s) were synthesized by cyclization of carboxylic acid group of 2-(2-methoxy-4-(3-oxo-3-substituted phenylprop-1-enyl)phenoxy) acetic acid (4a–s) with thiosemicarbazide in the presence of POCl3 or PPA. The stru...

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Main Authors: Malleshappa N. Noolvi, Harun M. Patel, Sarita Kamboj, Swaranjit Singh Cameotra
Format: Article
Language:English
Published: Elsevier 2016-11-01
Series:Arabian Journal of Chemistry
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1878535212000305
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author Malleshappa N. Noolvi
Harun M. Patel
Sarita Kamboj
Swaranjit Singh Cameotra
author_facet Malleshappa N. Noolvi
Harun M. Patel
Sarita Kamboj
Swaranjit Singh Cameotra
author_sort Malleshappa N. Noolvi
collection DOAJ
description A series of 1,3,4-thiadiazole derivatives of 2-(4-formyl-2-methoxyphenoxy) acetic acid (6a–s) were synthesized by cyclization of carboxylic acid group of 2-(2-methoxy-4-(3-oxo-3-substituted phenylprop-1-enyl)phenoxy) acetic acid (4a–s) with thiosemicarbazide in the presence of POCl3 or PPA. The structures of the compounds were confirmed by IR, 1H NMR and mass analysis. All the compounds have been evaluated in vitro for their antimicrobial activities against several strains of microbes and show significant activity.
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spelling doaj.art-b9b03707b7ca4731a642fa0fdbae833d2022-12-22T01:15:24ZengElsevierArabian Journal of Chemistry1878-53522016-11-019S2S1283S128910.1016/j.arabjc.2012.02.003Synthesis and antimicrobial evaluation of novel 1,3,4-thiadiazole derivatives of 2-(4-formyl-2-methoxyphenoxy) acetic acidMalleshappa N. Noolvi0Harun M. Patel1Sarita Kamboj2Swaranjit Singh Cameotra3Department of Pharmaceutical Chemistry, Shree Dhanvantary Pharmacy College, Kim (Surat) 394110, Gujarat, IndiaDepartment of Pharmaceutical Chemistry, R.C. Patel Institute of Pharmaceutical Education and Research, Shirpur (Dhule) 425405, Maharashtra, IndiaDepartment of Pharmaceutical Chemistry, ASBASJSM College of Pharmacy, Bela (Ropar) 140111, Punjab, IndiaEnvironmental Biotechnology & Microbial Biochemistry, Institute of Microbial Technology, Chandigarh, IndiaA series of 1,3,4-thiadiazole derivatives of 2-(4-formyl-2-methoxyphenoxy) acetic acid (6a–s) were synthesized by cyclization of carboxylic acid group of 2-(2-methoxy-4-(3-oxo-3-substituted phenylprop-1-enyl)phenoxy) acetic acid (4a–s) with thiosemicarbazide in the presence of POCl3 or PPA. The structures of the compounds were confirmed by IR, 1H NMR and mass analysis. All the compounds have been evaluated in vitro for their antimicrobial activities against several strains of microbes and show significant activity.http://www.sciencedirect.com/science/article/pii/S1878535212000305Phenoxyacetic acid1,3,4-ThiadiazoleAntimicrobial
spellingShingle Malleshappa N. Noolvi
Harun M. Patel
Sarita Kamboj
Swaranjit Singh Cameotra
Synthesis and antimicrobial evaluation of novel 1,3,4-thiadiazole derivatives of 2-(4-formyl-2-methoxyphenoxy) acetic acid
Arabian Journal of Chemistry
Phenoxyacetic acid
1,3,4-Thiadiazole
Antimicrobial
title Synthesis and antimicrobial evaluation of novel 1,3,4-thiadiazole derivatives of 2-(4-formyl-2-methoxyphenoxy) acetic acid
title_full Synthesis and antimicrobial evaluation of novel 1,3,4-thiadiazole derivatives of 2-(4-formyl-2-methoxyphenoxy) acetic acid
title_fullStr Synthesis and antimicrobial evaluation of novel 1,3,4-thiadiazole derivatives of 2-(4-formyl-2-methoxyphenoxy) acetic acid
title_full_unstemmed Synthesis and antimicrobial evaluation of novel 1,3,4-thiadiazole derivatives of 2-(4-formyl-2-methoxyphenoxy) acetic acid
title_short Synthesis and antimicrobial evaluation of novel 1,3,4-thiadiazole derivatives of 2-(4-formyl-2-methoxyphenoxy) acetic acid
title_sort synthesis and antimicrobial evaluation of novel 1 3 4 thiadiazole derivatives of 2 4 formyl 2 methoxyphenoxy acetic acid
topic Phenoxyacetic acid
1,3,4-Thiadiazole
Antimicrobial
url http://www.sciencedirect.com/science/article/pii/S1878535212000305
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