Synthesis and Microbial Activities of 2, 5, 6-Substituted Benzimidazole Derivatives

Authors

Dhondiba Vishwanath

GWFGC Kalaburagi, Karnataka (India)

Devaraju

Yuvaraja college Mysore, Karnataka (India)

Vijayanand Vithalrao

GC(Autonomous) kalaburagi, Karnataka (India)

Article Information

DOI: 10.51584/IJRIAS.2025.101100038

Subject Category: Chemistry

Volume/Issue: 10/11 | Page No: 392-398

Publication Timeline

Submitted: 2025-11-24

Accepted: 2025-11-30

Published: 2025-12-09

Abstract

Benzimidazole derivatives are the analogues of purine nucleosides which are found in human body. These are an important heterocyclic organic compounds containing phenyl ring (six membered ring) fused with imidazole (five membered ring) which possesses wide range of starting material for various compounds and exhibit clinical applications such as anti-inflammatory, antibacterial, antifungal, antiviral, analgesic, proton pump inhibitors, antihistamines, anticancer, etc. The presence of electron-donating groups (OH, -CH3, -OCH3) causes significant increase in the biological activity, while the electron-withdrawing groups (-Cl, -Br,–NO2) decreases the biological activity of synthesized of benzimidazole derivatives.

Keywords

Benzimidazole; 4,5-substituted phenylene-1,2-diamine

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