Synthesis of New Structural Thiosemicarbazones and Investigation of Their Antibacterial Activities Against E. Coli

Abstract

This study focuses on the synthesis and characterization of novel thiosemicarbazone derivatives with potential antibacterial activity. Through a systematic two‐step synthesis process, involving the preparation of substitute aldehydes (A1–A6) followed by the formation of thiosemicarbazone derivatives (S1–S6), novel compounds (S1, S2) were successfully obtained. The structures of the synthesized compounds were thoroughly characterized using FT‐IR, ¹H‐NMR, ¹³C‐NMR, LC/MS, UV‐Vis, and SEM‐EDX. The results highlight the significance of sulfuric acid as a catalyst in the synthesis of pyrazole‐thiosemicarbazide derivatives (S1, S2), demonstrating its superior efficiency compared to acetic acid. The compounds exhibited varying degrees of antibacterial activity against E. coli, with compounds S3–S6 showing promising results with MIC values below 25 mg/mL. These findings indicate the potential of these compounds as antibacterial agents. Overall, the successful synthesis and characterization of these novel derivatives open avenues for further research into their potential pharmacological applications. The findings of this study lay the foundation for future studies aimed at optimizing these compounds for enhanced antimicrobial activity and exploring their therapeutic potential in treating bacterial infections.