Abstract
This report describes an efficient and mild approach for the synthesis of Piperastrol and Enastron via a one-pot three-component cyclocondensation reaction employing ammonium sulfocyanate (NH4SCN) on gram scale in isopropyl alcohol–PEG 400 medium. In this reaction, ammonium sulfocyanate is not only the reacting component but also accelerates the rate of reaction to afford Biginelli compounds. High yields, short reaction time and easy workup procedure are the key advantages of the present protocol. Ammonium sulfocyanate is readily available, cheaper, safer and industrially acceptable inorganic salt.
Keywords: Enastron, piperastrol, catalyst free, ammonium sulfocyanate, biginelli reaction, anticancer.
Letters in Organic Chemistry
Title:New Strategy for Synthesis of Anticancer Active Piperastrol, Enastron Using Ammonium Sulfocyanate
Volume: 18 Issue: 11
Author(s): Santoshkumar M. Potdar*, Aishwarya R. Deshmukh and Krishnakant T. Waghmode
Affiliation:
- Department of Chemistry, D.G. Ruparel College, Mumbai - 400016, Maharashtra,India
Keywords: Enastron, piperastrol, catalyst free, ammonium sulfocyanate, biginelli reaction, anticancer.
Abstract: This report describes an efficient and mild approach for the synthesis of Piperastrol and Enastron via a one-pot three-component cyclocondensation reaction employing ammonium sulfocyanate (NH4SCN) on gram scale in isopropyl alcohol–PEG 400 medium. In this reaction, ammonium sulfocyanate is not only the reacting component but also accelerates the rate of reaction to afford Biginelli compounds. High yields, short reaction time and easy workup procedure are the key advantages of the present protocol. Ammonium sulfocyanate is readily available, cheaper, safer and industrially acceptable inorganic salt.
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Cite this article as:
Potdar M. Santoshkumar *, Deshmukh R. Aishwarya and Waghmode T. Krishnakant , New Strategy for Synthesis of Anticancer Active Piperastrol, Enastron Using Ammonium Sulfocyanate, Letters in Organic Chemistry 2021; 18 (11) . https://dx.doi.org/10.2174/1570178617999201006200102
DOI https://dx.doi.org/10.2174/1570178617999201006200102 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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