Synthesis and Microbial Activity of Novel 3-Methyl-2-pyrazolin-5-one Derivatives

2-Oxo-2H-chromene-3-carbohydrazide derivatives 2a,b react with 2-{[4-(substituted thiazol-2-yl)iminoethyl)-phenyl]hydrazono}-3-oxo-butyric acid ethyl esters 4a–c to give 3-methyl-1-[(2-oxo-2H-chromen-3-yl) carbonyl]-4-{[4-(substituted thiazol-2-yl)iminoethyl)-phenyl]hydrazono}]-2-pyrazolin-5-one der...

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Main Authors: Mohamed S. Mostafa, Nasser M. Abd El-Salam, Othman Y. Alothman
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:Journal of Chemistry
Online Access:http://dx.doi.org/10.1155/2013/183130
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author Mohamed S. Mostafa
Nasser M. Abd El-Salam
Othman Y. Alothman
author_facet Mohamed S. Mostafa
Nasser M. Abd El-Salam
Othman Y. Alothman
author_sort Mohamed S. Mostafa
collection DOAJ
description 2-Oxo-2H-chromene-3-carbohydrazide derivatives 2a,b react with 2-{[4-(substituted thiazol-2-yl)iminoethyl)-phenyl]hydrazono}-3-oxo-butyric acid ethyl esters 4a–c to give 3-methyl-1-[(2-oxo-2H-chromen-3-yl) carbonyl]-4-{[4-(substituted thiazol-2-yl)iminoethyl)-phenyl]hydrazono}]-2-pyrazolin-5-one derivatives 5a–f. A considerable increase in the reaction rate had been observed with better yield using microwave irradiation for the synthesis of compounds 2a, b, 3a–c, and 5a–f. The synthesized products were tested against B. subtilis, S. aureus, and E. coli as well as C. albicans compared with tetracycline and nystatin as reference drugs.
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institution Kabale University
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spelling doaj-art-1692c9daca644292b0a37ed83733e5212025-02-03T01:21:54ZengWileyJournal of Chemistry2090-90632090-90712013-01-01201310.1155/2013/183130183130Synthesis and Microbial Activity of Novel 3-Methyl-2-pyrazolin-5-one DerivativesMohamed S. Mostafa0Nasser M. Abd El-Salam1Othman Y. Alothman2Chemistry Department, Faculty of Science, Jazan University, P.O. Box 2079, Saudi ArabiaRiyadh Community College, King Saud University, P.O. Box 28095, Riyadh 11437, Saudi ArabiaDepartment of Chemical Engineering, College of Engineering, King Saud University, P.O. Box 800, Riyadh 11421, Saudi Arabia2-Oxo-2H-chromene-3-carbohydrazide derivatives 2a,b react with 2-{[4-(substituted thiazol-2-yl)iminoethyl)-phenyl]hydrazono}-3-oxo-butyric acid ethyl esters 4a–c to give 3-methyl-1-[(2-oxo-2H-chromen-3-yl) carbonyl]-4-{[4-(substituted thiazol-2-yl)iminoethyl)-phenyl]hydrazono}]-2-pyrazolin-5-one derivatives 5a–f. A considerable increase in the reaction rate had been observed with better yield using microwave irradiation for the synthesis of compounds 2a, b, 3a–c, and 5a–f. The synthesized products were tested against B. subtilis, S. aureus, and E. coli as well as C. albicans compared with tetracycline and nystatin as reference drugs.http://dx.doi.org/10.1155/2013/183130
spellingShingle Mohamed S. Mostafa
Nasser M. Abd El-Salam
Othman Y. Alothman
Synthesis and Microbial Activity of Novel 3-Methyl-2-pyrazolin-5-one Derivatives
Journal of Chemistry
title Synthesis and Microbial Activity of Novel 3-Methyl-2-pyrazolin-5-one Derivatives
title_full Synthesis and Microbial Activity of Novel 3-Methyl-2-pyrazolin-5-one Derivatives
title_fullStr Synthesis and Microbial Activity of Novel 3-Methyl-2-pyrazolin-5-one Derivatives
title_full_unstemmed Synthesis and Microbial Activity of Novel 3-Methyl-2-pyrazolin-5-one Derivatives
title_short Synthesis and Microbial Activity of Novel 3-Methyl-2-pyrazolin-5-one Derivatives
title_sort synthesis and microbial activity of novel 3 methyl 2 pyrazolin 5 one derivatives
url http://dx.doi.org/10.1155/2013/183130
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