Abstract
Some new 3-[7-methoxy-2H-1-benzopyran-2-one-4-yl]-1-(coumarin-3-yl)prop-2-en-1-ones 5a-d (dicoumarinyl chalcones) were synthesized by Wittig reaction of 3-[(triphenylphosphinyl)acetenyl]coumarins 3a-d and 7-methoxy-4- formylcoumarin 4. These chalcones were then utilized for the synthesis of dicoumarinyl pyrazolines 6a-h and 7a-l under microwave irradiation. All the synthesized compounds 5a-d, 6a-h and 7a-l were characterized by IR, 1H NMR, 13C NMR, mass spectral data and elemental analysis. The compounds were subjected to in vitro antimicrobial screening against a representative panel of bacteria (Bacillus subtilis, Staphylococcus aureus, Escherichia coli, Salmonella typhi) and fungi (Aspergillus niger, Candida albicans).
Keywords: Antimicrobial screening, aspergillus niger, bacillus subtilis, broth dilution method, candida albicans, diastereotopic protons, dicoumarinyl chalcones, dicoumarinyl pyrazolines, escherichia coli, 7-methoxy-4-formylcoumarin, microwave irradiation, salmonella typhi, staphylococcus aureus, 3-[(triphenylphosphinyl)- acetenyl]coumarins, wittig reaction.
Graphical Abstract
Current Microwave Chemistry
Title:Microwave Assisted Preparation of New Dicoumarinyl Pyrazoline Derivatives as Antimicrobials
Volume: 1 Issue: 1
Author(s): Hemali B. Lad, Rakesh R. Giri, Chirag V. Patel, Varun G. Bhila and Dinkar I. Brahmbhatt
Affiliation:
Keywords: Antimicrobial screening, aspergillus niger, bacillus subtilis, broth dilution method, candida albicans, diastereotopic protons, dicoumarinyl chalcones, dicoumarinyl pyrazolines, escherichia coli, 7-methoxy-4-formylcoumarin, microwave irradiation, salmonella typhi, staphylococcus aureus, 3-[(triphenylphosphinyl)- acetenyl]coumarins, wittig reaction.
Abstract: Some new 3-[7-methoxy-2H-1-benzopyran-2-one-4-yl]-1-(coumarin-3-yl)prop-2-en-1-ones 5a-d (dicoumarinyl chalcones) were synthesized by Wittig reaction of 3-[(triphenylphosphinyl)acetenyl]coumarins 3a-d and 7-methoxy-4- formylcoumarin 4. These chalcones were then utilized for the synthesis of dicoumarinyl pyrazolines 6a-h and 7a-l under microwave irradiation. All the synthesized compounds 5a-d, 6a-h and 7a-l were characterized by IR, 1H NMR, 13C NMR, mass spectral data and elemental analysis. The compounds were subjected to in vitro antimicrobial screening against a representative panel of bacteria (Bacillus subtilis, Staphylococcus aureus, Escherichia coli, Salmonella typhi) and fungi (Aspergillus niger, Candida albicans).
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Lad B. Hemali, Giri R. Rakesh, Patel V. Chirag, Bhila G. Varun and Brahmbhatt I. Dinkar, Microwave Assisted Preparation of New Dicoumarinyl Pyrazoline Derivatives as Antimicrobials, Current Microwave Chemistry 2014; 1 (1) . https://dx.doi.org/10.2174/221333560101140519152017
DOI https://dx.doi.org/10.2174/221333560101140519152017 |
Print ISSN 2213-3356 |
Publisher Name Bentham Science Publisher |
Online ISSN 2213-3364 |
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