Abstract

In the present study two series of novel imidazole derivatives containing substituted pyrazole moiety ( 3a– d and 5a– j) were synthesized. The first series were synthesized by the reaction of 3-aryl-1 H-pyrazole-4-carbaldehyde thiosemicarbazones ( 2a– d) with DMAD and the second series by the reaction of 3-aryl-1 H-pyrazole-4-carbaldehydes ( 1a– e) with 1,2-diketones ( 4a,b) in the presence of ammonium acetate. Structures of newly synthesized compounds were characterized by spectral studies. New compounds were screened for antifungal and antibacterial activities. Among the synthesized compounds, compound 3c was found to be potent antimicrobial agent. The acute oral toxicity study for the compound 3c was carried out and the experimental studies revealed that compound 3c is safe up to 3000 mg/kg and no death of animals were recorded.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.