Design, Synthesis and Evaluation of Schiff’s Bases of 4-Chloro-3-coumarin aldehyde as Antimicrobial Agents

4-Chloro-2-oxo-2H-chromene-3-carbaldehyde (2) was reacted with different anilines in rectified spirit as solvent to yield a series of the title compounds i.e. 4-chloro-3-((substituted-phenylimino) methyl)-2H-chromen-2-one (3a-i). These compounds were charaterised on the basis of their spectral (IR,...

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Main Authors: Shriram Bairagi, Ashok Bhosale, Meenakshi N. Deodhar
Format: Article
Language:English
Published: Wiley 2009-01-01
Series:E-Journal of Chemistry
Online Access:http://dx.doi.org/10.1155/2009/874389
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author Shriram Bairagi
Ashok Bhosale
Meenakshi N. Deodhar
author_facet Shriram Bairagi
Ashok Bhosale
Meenakshi N. Deodhar
author_sort Shriram Bairagi
collection DOAJ
description 4-Chloro-2-oxo-2H-chromene-3-carbaldehyde (2) was reacted with different anilines in rectified spirit as solvent to yield a series of the title compounds i.e. 4-chloro-3-((substituted-phenylimino) methyl)-2H-chromen-2-one (3a-i). These compounds were charaterised on the basis of their spectral (IR, 1H NMR) data and evaluated for antimicrobial activity in vitro against gram positive and gram negative bacteria and fungi. Compound 3C was found to be most active with an MIC of 15 μg /mL against all the tested organisms.
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publishDate 2009-01-01
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series E-Journal of Chemistry
spelling doaj-art-74bdbda5adce4516a98b3c50e87ed7882025-02-03T06:44:20ZengWileyE-Journal of Chemistry0973-49452090-98102009-01-016375976210.1155/2009/874389Design, Synthesis and Evaluation of Schiff’s Bases of 4-Chloro-3-coumarin aldehyde as Antimicrobial AgentsShriram Bairagi0Ashok Bhosale1Meenakshi N. Deodhar2Department of Pharmaceutical Chemistry, SGRS College of Pharmacy, Saswad, Pune-412301, IndiaDepartment of Pharmaceutical Chemistry, SGRS College of Pharmacy, Saswad, Pune-412301, IndiaDepartment of Pharmaceutical Chemistry, SGRS College of Pharmacy, Saswad, Pune-412301, India4-Chloro-2-oxo-2H-chromene-3-carbaldehyde (2) was reacted with different anilines in rectified spirit as solvent to yield a series of the title compounds i.e. 4-chloro-3-((substituted-phenylimino) methyl)-2H-chromen-2-one (3a-i). These compounds were charaterised on the basis of their spectral (IR, 1H NMR) data and evaluated for antimicrobial activity in vitro against gram positive and gram negative bacteria and fungi. Compound 3C was found to be most active with an MIC of 15 μg /mL against all the tested organisms.http://dx.doi.org/10.1155/2009/874389
spellingShingle Shriram Bairagi
Ashok Bhosale
Meenakshi N. Deodhar
Design, Synthesis and Evaluation of Schiff’s Bases of 4-Chloro-3-coumarin aldehyde as Antimicrobial Agents
E-Journal of Chemistry
title Design, Synthesis and Evaluation of Schiff’s Bases of 4-Chloro-3-coumarin aldehyde as Antimicrobial Agents
title_full Design, Synthesis and Evaluation of Schiff’s Bases of 4-Chloro-3-coumarin aldehyde as Antimicrobial Agents
title_fullStr Design, Synthesis and Evaluation of Schiff’s Bases of 4-Chloro-3-coumarin aldehyde as Antimicrobial Agents
title_full_unstemmed Design, Synthesis and Evaluation of Schiff’s Bases of 4-Chloro-3-coumarin aldehyde as Antimicrobial Agents
title_short Design, Synthesis and Evaluation of Schiff’s Bases of 4-Chloro-3-coumarin aldehyde as Antimicrobial Agents
title_sort design synthesis and evaluation of schiff s bases of 4 chloro 3 coumarin aldehyde as antimicrobial agents
url http://dx.doi.org/10.1155/2009/874389
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AT meenakshindeodhar designsynthesisandevaluationofschiffsbasesof4chloro3coumarinaldehydeasantimicrobialagents