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Research Articles

Synthesis and Antimicrobial Screening of 3-Fluoromethyl Pyrazole Derivatives

, , , , &
Pages 3640-3650 | Received 20 Jul 2021, Accepted 02 May 2022, Published online: 18 May 2022
 

Abstract

A new series of 1-(5-(4-alkoxy-3-(methylsulfonyl)phenyl)thiophen-2-yl)-5-substituted-3-(trifluoromethyl)-1H-pyrazole have been synthesized by a cyclocondensation reaction of 1,1,1-trifluoropentane-2,4-dione (1a) with (5-(4-methoxy-3-(methylsulfonyl)phenyl)thiophen-2-yl)hydrazine (2). The structure of 1-(5-(4-alkoxy-3-(methylsulfonyl)phenyl)thiophen-2-yl)-5-substituted-3-(trifluoromethyl)-1H-pyrazole derivatives was characterized by spectroscopic analysis. The synthesized 3-(trifluoromethyl)-1H-pyrazole derivatives were screened for in vitro antibacterial activity against Escherichia coli (NCIM 2574), Proteus mirabilis (NCIM 2388) Bacillus subtilis (NCIM 2063) and Staphylococcus albus (NCIM 2178) and in vitro antifungal activity against Candida albicans (NCIM 3100) and Aspergillus niger (ATCC 504). The compounds 4-(5-(5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)thiophen-2-yl)-2-(methylsulfonyl)phenol (4) and 1-methyl-4-(4-(5-(5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)thiophen-2-yl)-2-(methylsulfonyl)phenoxy)pyrrolidin-2-one (6e) showed moderate to good antibacterial and antifungal activity.

Acknowledgments

Authors would like to acknowledge to S. P. Mandali Pune and Late. Dr. T. R. Ingale family for providing infrastructure facilities. Authors would like to thanks CIF-SPPU, Pune and IISER, Pune for spectral analysis. S. P. Mandali’s Bhide Foundation Pune has acknowledged for lending support with their biological activities.

Disclosure statement

There are no conflicts to declare.

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