Studies on Synthesis of N-1 Fused Heterocyclic Derivatives Using Potassium Carbonate and PEG- 400 as Green Catalyst

Authors

  • Anjali M. Wanegaonkar Bharati Vidyapeeth College of Pharmacy, Sector-8, CBD Belapur - Navi Mumbai- 400614, Maharashtra, India.
  • Milind J. Bhitre Deptartment of Pharmaceutical Chemistry C. U. Shah College of Pharmacy, S. N. D. T. Women’s University, Sir Vithaldas Vidyavihar, Juhu Road, Santacruz (West), Mumbai- 400 049, Maharashtra, India.

DOI:

https://doi.org/10.9734/bpi/tipr/v10/11966D

Keywords:

2-acetyl –Benzimidazole, Indole-3-Carboxaldehyde, green synthesis, PTC

Abstract

Due to their synthetic utility and extensive variety of pharmacological effects, indole and benzimidazole, as well as their substituted derivatives, help to draw interest. The N-substituted fused heterocyclic compounds are usually physiologically active and could be employed as antitumor medicines. The various reactions reported that reactions of K2CO3 showing its essentiality for a particular reaction due to its characteristics like solubility in water, mild base character, easy availability, eco-friendly, and nontoxic in nature. In the presence and absence of phase transfer catalyst such as PEG-400 and TEBAC, the effect of the ratio of catalyst used anhydrous K2CO3 for its N-1 alkylation or arylation of indole-3-carboxaldehyde and 2-acetylbenzimidazole is observed. The ratio 1:4 of anhydrous K2CO3 along with PEG-400 gives, ease of catalyst handling, mild reaction conditions and reactions carried out at 10-15ºC temperature with excellent yields. The simplicity of the approach makes it attractive for the synthesis of N-fused heterocyclic derivatives that could be employed as biological substitutes.

Published

2021-08-03

How to Cite

Anjali M. Wanegaonkar, & Milind J. Bhitre. (2021). Studies on Synthesis of N-1 Fused Heterocyclic Derivatives Using Potassium Carbonate and PEG- 400 as Green Catalyst. Technological Innovation in Pharmaceutical Research Vol. 10, 88–95. https://doi.org/10.9734/bpi/tipr/v10/11966D