An efficient Iodine Catalyzed Microwave Assisted One-Pot Multicomponent Synthesis of 5-amino-1, 3-diphenyl-1H-pyrazole4-carbonitrile and its derivatives.

The development of eco-friendly, time-efficient, and high-yielding synthetic methodologies for heterocyclic scaffolds remains a central focus in modern organic chemistry. In this study, we report an efficient iodine-catalyzed, microwave-assisted one-pot multicomponent protocol for the synthesis of amino pyrazoles and their derivatives. The synergistic effect of iodine catalysis and microwave irradiation significantly enhances reaction rates, minimizes by-product formation, and affords the desired amino pyrazoles in excellent yields within short reaction times. The operational simplicity, environmental benignity, and atom-economy of the method highlight its superiority over conventional protocols. Structural elucidation of the synthesized derivatives was achieved through spectral (FT-IR, 1H NMR, 13C NMR, and Mass) analyses. Furthermore, the synthesized compounds, bearing diverse functional substitutions, demonstrate promising potential for biological applications, as pyrazole-based frameworks are well-documented for their antioxidant activity.

Authors

Publication Details

Journal
International Journal of Pharmaceutical Research and Applications
Published
2025-04-01
DOI
https://doi.org/10.35629/4494-100412671272
Primary Topic
Multicomponent Synthesis of Heterocycles
Type
article
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article

An efficient Iodine Catalyzed Microwave Assisted One-Pot Multicomponent Synthesis of 5-amino-1, 3-diphenyl-1H-pyrazole4-carbonitrile and its derivatives.

B.N.Chate B.N.Chate, Rohit Gaikwad
International Journal of Pharmaceutical Research and Applications
Multicomponent Synthesis of Heterocycles
article

An efficient Iodine Catalyzed Microwave Assisted One-Pot Multicomponent Synthesis of 5-amino-1, 3-diphenyl-1H-pyrazole4-carbonitrile and its derivatives.

B.N.Chate B.N.Chate, Rohit Gaikwad
article en

Abstract

The development of eco-friendly, time-efficient, and high-yielding synthetic methodologies for heterocyclic scaffolds remains a central focus in modern organic chemistry. In this study, we report an efficient iodine-catalyzed, microwave-assisted one-pot multicomponent protocol for the synthesis of amino pyrazoles and their derivatives. The synergistic effect of iodine catalysis and microwave irradiation significantly enhances reaction rates, minimizes by-product formation, and affords the desired amino pyrazoles in excellent yields within short reaction times. The operational simplicity, environmental benignity, and atom-economy of the method highlight its superiority over conventional protocols. Structural elucidation of the synthesized derivatives was achieved through spectral (FT-IR, 1H NMR, 13C NMR, and Mass) analyses. Furthermore, the synthesized compounds, bearing diverse functional substitutions, demonstrate promising potential for biological applications, as pyrazole-based frameworks are well-documented for their antioxidant activity.

International Journal of Pharmaceutical Research and ApplicationsVol. 10(4)
Openalex Percentile: Top 82%
Multicomponent Synthesis of Heterocycles
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