An Efficient Synthesis of 1H-Pyrazolo [3, 4-B]Quinolones Derivatives Catalyzed by MSA in Aqueous Media Under Ultrasound Irradiation

A novel, eco-friendly, and highly efficient method has been developed for the synthesis of 1Hpyrazolo[3,4-b]quinolonederivatives using methanesulfonic acid (MSA) as a catalyst in aqueous medium under ultrasound irradiation. This approach integrates the principles of green chemistry by employing water as a benign solvent and MSA as a biodegradable, non-volatile Brønsted acid catalyst. Ultrasound irradiation significantly accelerates the reaction through acoustic cavitation, leading to enhanced yields and reduced reaction times under mild conditions. The methodology is operationally simple, offers excellent chemoselectivity, and provides good to excellent yields of the desired fused heterocyclic products. The synthesized compounds were thoroughly characterized using IR, ¹H NMR, ¹³C NMR, and mass spectrometry. This protocol represents a sustainable and scalable alternative for the construction of biologically relevant pyrazoloquinolone scaffolds, with potential applications in pharmaceutical and medicinal chemistry.

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Publication Details

Journal
International Journal of Pharmaceutical Research and Applications
Published
2025-04-01
DOI
https://doi.org/10.35629/4494-1004462465
Primary Topic
Synthesis and Characterization of Heterocyclic Compounds
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article
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article

An Efficient Synthesis of 1H-Pyrazolo [3, 4-B]Quinolones Derivatives Catalyzed by MSA in Aqueous Media Under Ultrasound Irradiation

Amol V. Sapkal
International Journal of Pharmaceutical Research and Applications
Synthesis and Characterization of Heterocyclic Compounds
article

An Efficient Synthesis of 1H-Pyrazolo [3, 4-B]Quinolones Derivatives Catalyzed by MSA in Aqueous Media Under Ultrasound Irradiation

Amol V. Sapkal
article en

Abstract

A novel, eco-friendly, and highly efficient method has been developed for the synthesis of 1Hpyrazolo[3,4-b]quinolonederivatives using methanesulfonic acid (MSA) as a catalyst in aqueous medium under ultrasound irradiation. This approach integrates the principles of green chemistry by employing water as a benign solvent and MSA as a biodegradable, non-volatile Brønsted acid catalyst. Ultrasound irradiation significantly accelerates the reaction through acoustic cavitation, leading to enhanced yields and reduced reaction times under mild conditions. The methodology is operationally simple, offers excellent chemoselectivity, and provides good to excellent yields of the desired fused heterocyclic products. The synthesized compounds were thoroughly characterized using IR, ¹H NMR, ¹³C NMR, and mass spectrometry. This protocol represents a sustainable and scalable alternative for the construction of biologically relevant pyrazoloquinolone scaffolds, with potential applications in pharmaceutical and medicinal chemistry.

International Journal of Pharmaceutical Research and ApplicationsVol. 10(4)
Openalex Percentile: Top 86%
Synthesis and Characterization of Heterocyclic Compounds
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An Efficient Synthesis of 1H-Pyrazolo [3, 4-B]Quinolones Derivatives Catalyzed by MSA in Aqueous Media Under Ultrasound Irradiation — Amol V. Sapkal · International Journal of Pharmaceutical Research and Applications (2025) | TGRS Research Map | TGRS