Synthesis, Identification, and Evaluation of Antibacterial Activity of Some New 4,5-Dihydro-1H-Pyrazoles, Derivatives from Substituted Chalcones

In this work, a series of new 4,5-dihydro-1H-pyrazole derivatives (M21-M25) has been synthesized successfully via the reaction of different aldehydes with ketones to produce chalcones, followed by the reaction with hydrazine and phenyl hydrazine. The prepared compounds were identified using FT-IR spectroscopy, 1H NMR spectroscopy, and 13C NMR spectroscopy. The biological activity of these prepared compounds was preliminarily evaluated against certain types of gram-positive (Staphylococcus aureus) and gram-negative (Escherichia coli). The results showed a high antibacterial effect towards both types of bacteria at high concentrations.

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Publication Details

Published
2025-09-25
DOI
https://doi.org/10.23939/chcht19.03.482
Primary Topic
Synthesis and biological activity
Type
article
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article

Synthesis, Identification, and Evaluation of Antibacterial Activity of Some New 4,5-Dihydro-1H-Pyrazoles, Derivatives from Substituted Chalcones

Saad Salim Jasim, Shakhawan Beebany, Jawdat Hilmi Abdulwahid
Synthesis and biological activity
article

Synthesis, Identification, and Evaluation of Antibacterial Activity of Some New 4,5-Dihydro-1H-Pyrazoles, Derivatives from Substituted Chalcones

Saad Salim Jasim, Shakhawan Beebany, Jawdat Hilmi Abdulwahid
article en

Abstract

In this work, a series of new 4,5-dihydro-1H-pyrazole derivatives (M21-M25) has been synthesized successfully via the reaction of different aldehydes with ketones to produce chalcones, followed by the reaction with hydrazine and phenyl hydrazine. The prepared compounds were identified using FT-IR spectroscopy, 1H NMR spectroscopy, and 13C NMR spectroscopy. The biological activity of these prepared compounds was preliminarily evaluated against certain types of gram-positive (Staphylococcus aureus) and gram-negative (Escherichia coli). The results showed a high antibacterial effect towards both types of bacteria at high concentrations.

Vol. 19(3)
Openalex Percentile: Top 80%
Synthesis and biological activity
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