SYNTHESIS, SPECTRAL STUDIES AND ANTIMICROBIAL ACTIVITY OF SCHIFF BASE DERIVATIVES CONTAINING IMIDAZOLE NUCLEUS

Imidazole is a heterocyclic and a 1,3-diazole, is classified as an alkaloid.[1] Clotrimazole and Miconazole are the two imidazole drugs introduced as topical antimycotics on the market.[2,3] Losartan potassium is a medication that acts as an antihypertensive agent taken orally[4-6] Losartan's synthesis requires 2-butyl-5-chloro-4- formyl-3H-imidazole which is one of its essential intermediates.[7,8] The Schiff base derivatives of (3a-3j) were synthesized by the condensation of Amide derivatives with 3-(hydrazino carbanoyl)-4-methoxybenzenesulfonamide in the presence of glacial acetic acid. The structures of newly synthesized compounds were confirmed based on 1H-NMR, mass spectra, and IR data. All the newly synthesized compounds were screened for their antibacterial activity against Gram +ve Bacteria Bacillus subtilis, Staphylococcus aureus, and Gram –ve Bacteria Escherichia coli, Pseudomonas aeruginosa and Fungi Aspergillus niger.

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2025-11-15
DOI
https://doi.org/10.5281/zenodo.17616239
Primary Topic
Synthesis of Tetrazole Derivatives
Type
article
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article

SYNTHESIS, SPECTRAL STUDIES AND ANTIMICROBIAL ACTIVITY OF SCHIFF BASE DERIVATIVES CONTAINING IMIDAZOLE NUCLEUS

Zenodo (CERN European Organization for Nuclear Research)
Synthesis of Tetrazole Derivatives
article

SYNTHESIS, SPECTRAL STUDIES AND ANTIMICROBIAL ACTIVITY OF SCHIFF BASE DERIVATIVES CONTAINING IMIDAZOLE NUCLEUS

article en

Abstract

Imidazole is a heterocyclic and a 1,3-diazole, is classified as an alkaloid.[1] Clotrimazole and Miconazole are the two imidazole drugs introduced as topical antimycotics on the market.[2,3] Losartan potassium is a medication that acts as an antihypertensive agent taken orally[4-6] Losartan's synthesis requires 2-butyl-5-chloro-4- formyl-3H-imidazole which is one of its essential intermediates.[7,8] The Schiff base derivatives of (3a-3j) were synthesized by the condensation of Amide derivatives with 3-(hydrazino carbanoyl)-4-methoxybenzenesulfonamide in the presence of glacial acetic acid. The structures of newly synthesized compounds were confirmed based on 1H-NMR, mass spectra, and IR data. All the newly synthesized compounds were screened for their antibacterial activity against Gram +ve Bacteria Bacillus subtilis, Staphylococcus aureus, and Gram –ve Bacteria Escherichia coli, Pseudomonas aeruginosa and Fungi Aspergillus niger.

Zenodo (CERN European Organization for Nuclear Research)
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Synthesis of Tetrazole Derivatives
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