Synthesis of Baclofen; an Alternative Approach

Authors

Mohammad Hassan Houshdar Tehrani1,*, Morteza Farnia1, Massoud Shalchian Nazer1
1Department of Pharmaceutical Chemistry, School of Pharmacy, Shaheed Beheshti University of Medical Sciences, Tehran, Iran
*Corresponding Author: Department of Pharmaceutical Chemistry, School of Pharmacy, Shaheed Beheshti University of Medical Sciences, Tehran, Iran. Email:[email protected]

IJ Pharmaceutical Research:Vol. 2, issue 1; 1-3
Published online:Nov 20, 2010
Article type:Research Article
Received:Apr 01, 2002
Accepted:Feb 01, 2003
How to Cite:Houshdar Tehrani MH, Farnia M, Shalchian Nazer M. Synthesis of Baclofen; an Alternative Approach. Iran J Pharm Res. 2022;2(1):e127600. doi: https://doi.org/10.22037/ijpr.2010.26

Abstract

γ -Aminobutiric acid (GABA), the major inhibitory neurotransmitter in the central nervous system has two major receptor subtypes (GABAA and GABAB). GABAB receptors are activated by the antispastic and muscle relaxant agent, Baclofen, which is a lipophilic derivative of GABA. Since 1962 several strategies have been reported for the synthesis of baclofen.In this study an approach has been made to synthesize baclofen in an alternative way. The key steps involved the condensation of p-chloro benzaldehyde with nitromethane and the reaction of β-nitro styrene thus prepared with malonate diethyl ester. Further reduction and decarboxylation of the product gave access to baclofen with a good yield.

Copyright

© 2022, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

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