Synthesis Of Schiff Bases Of Thiophene-2-Carboxaldehyde And Its Antimicrobial Synthesis of N-Substituted Phenyl-4-Thiophenyl-2-Azetidinones and its Antimicrobial Activity
Mohd. Idrees, Mohd.Siddique*, A. G. Doshi and A. W. Raut
Post Graduate Department of Chemistry,Shri Shivaji Science College, Morshi Road, Amravati-444 603 (India) *Vidya Bharti Mahavidyalaya, Amravati.
2-Thiophenylidine-substituted aniline condenses with acetyl chloride in presence of triethyl amine in benzene gives N-substituted phenyl-4-thiophenyl-2-azetidinones. The azetidinones structure were confirmed by spectral and chemical data. These azetidinones tested against test organism Staphylococcus aureus, Bacillus megatherium, Bacillus subtilis, Proteus vulgaris, Escherichia coli, Pseudomonas aeruginosa and MIC values are obtained by serial dilution method. Title compound were found effective against both Gram positive and Gram negative bacteria. The minimum inhibitary concentration (MIC) value are in the range of >3 to 200 μg/ml for both Gram positive and Gram negative bacteria.
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| Copy the following to cite this article: Idrees. M, Siddique. M, Doshi. A. G, Raut. A. W. Synthesis Of Schiff Bases Of Thiophene-2-Carboxaldehyde And Its Antimicrobial Synthesis of N-Substituted Phenyl-4-Thiophenyl-2-Azetidinones and its Antimicrobial Activity. Orient J Chem 2001;17(1). |
| Copy the following to cite this URL: Idrees. M, Siddique. M, Doshi. A. G, Raut. A. W. Synthesis Of Schiff Bases Of Thiophene-2-Carboxaldehyde And Its Antimicrobial Synthesis of N-Substituted Phenyl-4-Thiophenyl-2-Azetidinones and its Antimicrobial Activity. Orient J Chem 2001;17(1). Available from: http://www.orientjchem.org/?p=15553 |
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