Microwave Assisted Preparation of New Dicoumarinyl Pyrazoline Derivatives as Antimicrobials
Hemali B. Lad, Rakesh R. Giri, Chirag V. Patel, Varun G. Bhila and Dinkar I. Brahmbhatt
Pages 64-74 (11)
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).
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.
Department of Chemistry, Sardar Patel University, Vallabh Vidyanagar-388120, Gujarat, India.