Synthesis and characterization of substituted chalcone derivatives via pyrazole intermediates

This study explores the synthesis and characterization of a series of substituted chalcone derivatives via a multi-step synthetic methodology. The process involves the initial condensation of hydrazine derivatives with ethyl acetoacetate to form pyrazole derivatives as critical intermediates. Subsequent functionalization, including acylation and cyclization, was performed to yield the target chalcone derivatives. Reaction conditions were meticulously optimized, resulting in high-yield and high-purity compounds. The prepared compounds were characterized using Fourier-transform infrared (FT-IR) spectroscopy, proton nuclear magnetic resonance (¹H-NMR), and carbon-13 nuclear magnetic resonance (¹³C-NMR) spectroscopy, confirming their structures.

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Publication Details

Journal
International Journal of Applied Research
Published
2025-01-01
DOI
https://doi.org/10.22271/allresearch.2025.v11.i1c.12271
Primary Topic
Synthesis and biological activity
Type
article
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article

Synthesis and characterization of substituted chalcone derivatives via pyrazole intermediates

Mostafa M. Hamed, Safaa Ridah Shakor
International Journal of Applied Research
Synthesis and biological activity
article

Synthesis and characterization of substituted chalcone derivatives via pyrazole intermediates

Mostafa M. Hamed, Safaa Ridah Shakor
article en

Abstract

This study explores the synthesis and characterization of a series of substituted chalcone derivatives via a multi-step synthetic methodology. The process involves the initial condensation of hydrazine derivatives with ethyl acetoacetate to form pyrazole derivatives as critical intermediates. Subsequent functionalization, including acylation and cyclization, was performed to yield the target chalcone derivatives. Reaction conditions were meticulously optimized, resulting in high-yield and high-purity compounds. The prepared compounds were characterized using Fourier-transform infrared (FT-IR) spectroscopy, proton nuclear magnetic resonance (¹H-NMR), and carbon-13 nuclear magnetic resonance (¹³C-NMR) spectroscopy, confirming their structures.

International Journal of Applied ResearchVol. 11(1)
Openalex Percentile: Top 100%
Synthesis and biological activity
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