Synthesis, Characterization and Antimicrobial Evaluation of New Compounds Derived from 2-Mercaptobenzoxazole

The synthesis of a novel series of 2-mercaptobenzoxazole hydrazide(2-benzo[d]oxazol-2-ylthio) acetohydrazide) derivatives (3a-c, 4a, and 4b) through the use of various sulfonyl chlorides in dichloromethane and triethyl amine for the compounds (3a-c) and different aromatic aldehydes in the presence of glacial acetic acid for the compounds (4a, b). The novel compounds' anti-microbial effectiveness has been evaluated in vitro against two of (G+Ve) and two of (G-Ve) bacteria and for fungal activity. In comparison to other compounds, compounds (3a and 3b) had the most anti-microbial action against Candida albicans and pseudomonas aeruginosa, respectively, while compound (3c) was more effective against gram-positive bacteria (Streptococcus pyogenes) compare with other compounds. By using their ((melting point, Thin Layer Chromato-graphy , attenuated total reflectance-Fourier transform infrared (ATR-FTIR), and 1 HNMR, the target compounds were identified.

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Publication Details

Journal
Iraqi Journal of Pharmaceutical Sciences ( P-ISSN 1683 - 3597 E-ISSN 2521 - 3512)
Published
2025-09-20
DOI
https://doi.org/10.31351/vol34iss3pp12-17
Primary Topic
Synthesis and biological activity
Type
article
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article

Synthesis, Characterization and Antimicrobial Evaluation of New Compounds Derived from 2-Mercaptobenzoxazole

Mohammed Kamil Hadi, Zainab Dhia.k
Iraqi Journal of Pharmaceutical Sciences ( P-ISSN 1683 - 3597 E-ISSN 2521 - 3512)
Synthesis and biological activity
article

Synthesis, Characterization and Antimicrobial Evaluation of New Compounds Derived from 2-Mercaptobenzoxazole

Mohammed Kamil Hadi, Zainab Dhia.k
article en

Abstract

The synthesis of a novel series of 2-mercaptobenzoxazole hydrazide(2-benzo[d]oxazol-2-ylthio) acetohydrazide) derivatives (3a-c, 4a, and 4b) through the use of various sulfonyl chlorides in dichloromethane and triethyl amine for the compounds (3a-c) and different aromatic aldehydes in the presence of glacial acetic acid for the compounds (4a, b). The novel compounds' anti-microbial effectiveness has been evaluated in vitro against two of (G+Ve) and two of (G-Ve) bacteria and for fungal activity. In comparison to other compounds, compounds (3a and 3b) had the most anti-microbial action against Candida albicans and pseudomonas aeruginosa, respectively, while compound (3c) was more effective against gram-positive bacteria (Streptococcus pyogenes) compare with other compounds. By using their ((melting point, Thin Layer Chromato-graphy , attenuated total reflectance-Fourier transform infrared (ATR-FTIR), and 1 HNMR, the target compounds were identified.

Iraqi Journal of Pharmaceutical Sciences ( P-ISSN 1683 - 3597 E-ISSN 2521 - 3512)Vol. 34(3)
Openalex Percentile: Top 81%
Synthesis and biological activity
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