Synthesis, Characterisation and Evaluation of Azetidine-2-One Derivative

S. Ramachandran *

Department of Pharmaceutical Chemistry and Analysis, Vels Institute of Science Technology and Advanced Studies (VISTAS), Chennai-600 117, Tamilnadu, India.

S. Dheepika

Department of Pharmaceutical Chemistry and Analysis, Vels Institute of Science Technology and Advanced Studies (VISTAS), Chennai-600 117, Tamilnadu, India.

M. Deepak

Department of Pharmaceutical Chemistry and Analysis, Vels Institute of Science Technology and Advanced Studies (VISTAS), Chennai-600 117, Tamilnadu, India.

M. Duraiseelan

Department of Pharmaceutical Chemistry and Analysis, Vels Institute of Science Technology and Advanced Studies (VISTAS), Chennai-600 117, Tamilnadu, India.

B. S. Chandru

Department of Pharmaceutical Chemistry and Analysis, Vels Institute of Science Technology and Advanced Studies (VISTAS), Chennai-600 117, Tamilnadu, India.

M. Vijey Aanandhi

Department of Pharmaceutical Chemistry and Analysis, Vels Institute of Science Technology and Advanced Studies (VISTAS), Chennai-600 117, Tamilnadu, India.

*Author to whom correspondence should be addressed.


Abstract

Antibacterial, antifungal, anticancer, antitubercular, anti-HIV, analgesic, anti-inflammatory, and ulcerogenic activities have all been documented for azetidinone derivatives.

The reaction of Schiff base((Z)-N (4-dimethylamino)benzylidene)pyrimidine-2-amine) with chloroacetyl chloride yielded a novel chemical called Azetdine-2-one derivative. Fourier Transform Infrared Spectroscopy and Proton Nuclear Magnetic Resonance Spectroscopy were used to confirm the chemical structures of the produced substances. The antimicrobial activity shows that the compound showed mild Antibacterial activity against Staphylococcus aureus and Escherichia coli.

Keywords: Azetidine-2-one derivative, chloroacetyl chloride, Schiff Base


How to Cite

Ramachandran, S., S. Dheepika, M. Deepak, M. Duraiseelan, B. S. Chandru, and M. Vijey Aanandhi. 2022. “Synthesis, Characterisation and Evaluation of Azetidine-2-One Derivative”. Journal of Pharmaceutical Research International 34 (27A):41-44. https://doi.org/10.9734/jpri/2022/v34i27A35992.

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