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Synthesis and Antimicrobial Evaluation of Some Pyrazole Derivatives
AbstractReaction of a series of (E)-3-phenyl-4-(p-substituted phenyl)-3-buten-2-ones with p-sulfamylphenyl hydrazine in glacial acetic acid gave the corresponding hydrazones, subsequent treatment of which with 30% HCl afforded pyrazole-1-sulphonamides. On the other hand, refluxing of chalcones with either thiosemicarbazide or isonicotinic acid hydrazide in ethanol containing a few drops of acetic acid gave pyrazoline-1-thiocarboxamides and isonicotinoyl pyrazolines, respectively. The structures of the synthesized compounds were determined on the basis of their elemental analyses and spectroscopic data. The antimicrobial activity of the newly isolated heterocyclic compounds was evaluated against Gram-positive, Gram-negative bacteria and fungi. Most of the compounds showed a moderate degree of potent antimicrobial activity.
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Sharshira, E.M.; Hamada, N.M.M. Synthesis and Antimicrobial Evaluation of Some Pyrazole Derivatives. Molecules 2012, 17, 4962-4971.View more citation formats
Sharshira EM, Hamada NMM. Synthesis and Antimicrobial Evaluation of Some Pyrazole Derivatives. Molecules. 2012; 17(5):4962-4971.Chicago/Turabian Style
Sharshira, Essam Mohamed; Hamada, Nagwa Mohamed Mahrous. 2012. "Synthesis and Antimicrobial Evaluation of Some Pyrazole Derivatives." Molecules 17, no. 5: 4962-4971.