Synthesis, molecular docking and biological evaluation of coumarin based isoxazoles and benzoimidazoles

In this paper, we described the synthesis of coumarin moiety based Isoxazoles and Benzoimidazoles. The 4-hydroxy coumarin with POCl 3 were refluxed to get 4-chloro-2H-chromen-2-one which is reacted with 1-(2-mercapto-1H-benzo[d]imidazol-5-yl)ethanone will give compound (2). The cyclization of compounds (3a-e) with hydroxyl amine hydrochloride, resulted in corresponding coumarin isoxazoles (4a-e). The newly synthesized compounds’ structures were determined using elemental analysis, 1 H NMR, 13 C NMR and mass spectrum data. The compounds generated were evaluated for antimicrobial effects. Molecular docking studies were also carried out to know the inhibitory effect of the synthesized compounds.

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Publication Details

Journal
Main Group Chemistry
Published
2026-07-24
DOI
https://doi.org/10.1177/10241221261471640
Primary Topic
Synthesis and biological activity
Type
article
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article

Synthesis, molecular docking and biological evaluation of coumarin based isoxazoles and benzoimidazoles

Hanmanthu Guguloth, Damera Koteshwar
Main Group Chemistry
Synthesis and biological activity
article

Synthesis, molecular docking and biological evaluation of coumarin based isoxazoles and benzoimidazoles

Hanmanthu Guguloth, Damera Koteshwar
article en

Abstract

In this paper, we described the synthesis of coumarin moiety based Isoxazoles and Benzoimidazoles. The 4-hydroxy coumarin with POCl 3 were refluxed to get 4-chloro-2H-chromen-2-one which is reacted with 1-(2-mercapto-1H-benzo[d]imidazol-5-yl)ethanone will give compound (2). The cyclization of compounds (3a-e) with hydroxyl amine hydrochloride, resulted in corresponding coumarin isoxazoles (4a-e). The newly synthesized compounds’ structures were determined using elemental analysis, 1 H NMR, 13 C NMR and mass spectrum data. The compounds generated were evaluated for antimicrobial effects. Molecular docking studies were also carried out to know the inhibitory effect of the synthesized compounds.

Main Group Chemistry
Kakatiya University (IN)
Clean water and sanitation
Openalex Percentile: Top 16%
Synthesis and biological activity
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