Cs2CO3-mediated facile synthesis, characterizations, and biological activities of 4H-benzo[4,5]thiazolo[3,2-a]pyrimidin-4-ylidene)acetonitrile derivatives

In this study, we report the newer method for the synthesis of 4H-benzo[4,5]thiazolo[3,2-a]pyrimidin-4-ylidene) acetonitrile and the biological activities of the derivatives were systematically evaluated. The antimicrobial potential of the compounds was assessed against three bacterial and three fungal strains using the agar diffusion method. Among the derivatives tested, compounds 3b, 3e, and 3h demonstrated notable antibacterial and antifungal activities. Furthermore, the antioxidant capacity of the selected compounds was investigated through the DPPH radical scavenging assay. Compounds 3e and 3f exhibited significant radical scavenging activity, achieving effective inhibition at a concentration of 0.1 mg/mL. These findings highlight the promising antimicrobial and antioxidant properties of the investigated thiazolopyrimidine derivatives and support their potential for further biological and pharmacological studies.

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Publication Details

Journal
European Journal of Chemistry
Published
2026-03-31
DOI
https://doi.org/10.5155/eurjchem.17.1.13-18.2727
Primary Topic
Synthesis and biological activity
Type
article
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article

Cs2CO3-mediated facile synthesis, characterizations, and biological activities of 4H-benzo[4,5]thiazolo[3,2-a]pyrimidin-4-ylidene)acetonitrile derivatives

Gautam Prabhakar Sadawarte, A. K. Patil, Jamatsing Dabarsing Rajput, Pramod Pandurang Mahulikar et al.
European Journal of Chemistry
Synthesis and biological activity
article

Cs2CO3-mediated facile synthesis, characterizations, and biological activities of 4H-benzo[4,5]thiazolo[3,2-a]pyrimidin-4-ylidene)acetonitrile derivatives

Gautam Prabhakar Sadawarte, A. K. Patil, Jamatsing Dabarsing Rajput, Pramod Pandurang Mahulikar, Raosaheb Shivaji Patil
article en

Abstract

In this study, we report the newer method for the synthesis of 4H-benzo[4,5]thiazolo[3,2-a]pyrimidin-4-ylidene) acetonitrile and the biological activities of the derivatives were systematically evaluated. The antimicrobial potential of the compounds was assessed against three bacterial and three fungal strains using the agar diffusion method. Among the derivatives tested, compounds 3b, 3e, and 3h demonstrated notable antibacterial and antifungal activities. Furthermore, the antioxidant capacity of the selected compounds was investigated through the DPPH radical scavenging assay. Compounds 3e and 3f exhibited significant radical scavenging activity, achieving effective inhibition at a concentration of 0.1 mg/mL. These findings highlight the promising antimicrobial and antioxidant properties of the investigated thiazolopyrimidine derivatives and support their potential for further biological and pharmacological studies.

European Journal of ChemistryVol. 17(1)
Sant Gadge Baba Amravati University (IN), Kavayitri Bahinabai Chaudhari North Maharashtra University (IN), G.S. Science, Arts And Commerce College (IN)
Openalex Percentile: Top 29%
Synthesis and biological activity
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