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2000
Volume 24, Issue 5
  • ISSN: 1386-2073
  • E-ISSN: 1875-5402

Abstract

Aims and Objectives: Microwave-assisted condensation of acetophenone 1 and aromatic aldehydes 2 gave chalcone analogs 3, which were cyclized to pyrazole derivatives 6a-f via the reaction with hydrazine hydrate and oxalic acid in the presence of the catalytic amount of acetic acid in ethanol. Materials and Methods: The structural features of the synthesized compounds were characterized by melting point, FT-IR, 1H, 13C NMR and elemental analysis. Results: The antibacterial activities of the synthesized pyrazoles were evaluated against three gram-positive bacteria, such as Enterococcus durans, Staphylococcus aureus, Bacillus subtilis and two gram-negative bacteria such as Escherichia coli and Salmonella typhimurium. Conclusion: All the synthesized pyrazoles showed relatively high antibacterial activity against S. aureus strain, and none of them demonstrated antibacterial activity against E. coli.

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/content/journals/cchts/10.2174/1386207323666201019152206
2021-06-01
2025-04-10
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  • Article Type:
    Research Article
Keyword(s): 13C NMR; 1H NMR; antibacterial; chalcone; FT-IR; microwave assisted; Pyrazole
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