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September 10, 20250 citations

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

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RGRohit GaikwadBBB.N.Chate B.N.Chate

Key Points

  • The method achieves high yields of amino pyrazoles while minimizing by-products through iodine catalysis.
  • Reaction rates were significantly enhanced due to microwave-assisted techniques, leading to faster synthesis.
  • Structural characterization utilized spectral analyses, including FT-IR and NMR techniques for verification.
  • The approach emphasizes environmental friendliness and operational simplicity compared to conventional methods.

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.

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Cite This Study

Gaikwad et al. (2025) studied this question.

synapsesocial.com/papers/68c193de9b7b07f3a0617a5dhttps://doi.org/10.35629/4494-100412671272
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