An Innovative Protocol for Synthesis of 5-Cyanoindole: A Key Ingredient for Antidepressant Drug Vilazodone Hydrochloride

Authors

  • Muvvala Venkatanarayana Department of Chemistry, GITAM School of Science, GITAM (Deemed to be University), Hyderabad-502329, India.
  • H. Sharath Babu Department of Chemistry, GITAM School of Science, GITAM (Deemed to be University), Hyderabad-502329, India.
  • Ravi Nuchu Department of Chemistry, GITAM School of Science, GITAM (Deemed to be University), Hyderabad-502329, India.

DOI:

https://doi.org/10.9734/bpi/cmsdi/v4/837

Keywords:

5-Cyanoindole, vilazodone hydrochloride, ring closer reaction

Abstract

The synthesis of 5-cyanoindole, a common intermediate employed in several synthetic routes of vilazodone hydrochloride, an antidepressant drug, is described in this work. Because it avoids the use of heavy metals and cyanide reagents, the strategy was more eco-friendly than previously documented approaches. The protocol is also robust and commercially viable.  96% of 5-cyanoindole was produced by the cyclization reaction, which was accomplished in the presence of Fe/AcOH. The current protocol is appropriate for large-scale preparation in industry.

Published

2024-06-28

How to Cite

Muvvala Venkatanarayana, H. Sharath Babu, & Ravi Nuchu. (2024). An Innovative Protocol for Synthesis of 5-Cyanoindole: A Key Ingredient for Antidepressant Drug Vilazodone Hydrochloride. Chemical and Materials Sciences - Developments and Innovations Vol. 4, 141–150. https://doi.org/10.9734/bpi/cmsdi/v4/837