Publication Cover
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 53, 2023 - Issue 18
248
Views
1
CrossRef citations to date
0
Altmetric
Articles

Green and efficient three-component synthesis of novel isoniazid pyrazoles, molecular docking, antioxidant and antitubercular evaluation

, &
Pages 1506-1519 | Received 27 Apr 2023, Published online: 14 Jul 2023
 

Abstract

A series of novel isoniazid pyrazole derivatives were synthesized by an efficient, multicomponent reaction of various substituted aromatic aldehydes, isoniazid, and malononitrile in aqueous ethanol. The catalyst-free, green, three-component reaction took place well with good to excellent yields of the desired derivatives. The synthesized novel derivatives were screened for antimicrobial, antioxidant, and anti-TB properties along with the molecular docking study. Some of the synthesized compounds exhibit moderate antibacterial and comparable antifungal properties, while all of them display strong antioxidant activity. The compound 4l demonstrates the most significant activity against M. tuberculosis with MIC = 0.125 µg/mL. The various analytical techniques including FT-IR, 1H NMR, 13C NMR, and HRMS were utilized to confirm the structures of the newly synthesized compounds.

Graphical Abstract

Acknowledgments

The author, Bharti P. Koli acknowledged the financial assistance awarded for the research work from Mahatma Jyotiba Phule Research Fellowship (MJPRF-2021), Nagpur, Maharashtra, and SAP Scheme of Govt. of India for the financial support involved in the research work. R. P. Gore and P. R. Malasane are thankful to Ms. Deepali S. Ghorpade, Assistant Professor, Government College of Pharmacy, Amravati, Maharashtra for valuable discussion and input regarding docking study and SAIF, Punjab University, Chandigarh for spectral characterization. We are thankful to Dr. Mahesh Patil, Assistant Professor, Department of Microbiology, R. C. Patel A. S. C. College, Shirpur, Maharashtra, for the antimicrobial and antioxidant activities of the synthesized compounds. We are grateful to CSIR-Central Drug Research Institute, Lucknow for antitubercular activity.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Correction Statement

This article has been corrected with minor changes. These changes do not impact the academic content of the article.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.