From Surf Wiki (app.surf) — the open knowledge base
Levopropoxyphene
Levopropoxyphene is an antitussive. It is an optical isomer of dextropropoxyphene. The racemic mixture is called propoxyphene. Only the dextro-isomer (dextropropoxyphene) has an analgesic effect; the levo-isomer appears to exert only an antitussive effect. It was formerly marketed in the U.S. by Eli Lilly under the tradename Novrad (a reversal of Darvon) as an antitussive. Unlike many antitussives, it binds poorly to the sigma-1 receptor.
Synthesis

- Friedel-Crafts acylation of benzene with propionyl chloride and aluminium chloride as a Lewis acid.
- Mannich reaction of propiophenone with formaldehyde and dimethylamine affords the corresponding aminoketone.
- Reaction of the ketone with benzylmagnesium bromide gives the amino alcohol. It is of note that this intermediate fails to show analgesic activity in animal assays.
- Esterification of the alcohol by means of propionic anhydride affords the propionate.
Chirality
The presence of two chiral centers in this molecule means that the compound can exist as any of four isomers. The biologic activity has been found to be associated with the α-isomer. Resolution of that isomer into its optical antipodes showed the d isomer to be the active analgesic; this is now denoted as propoxyphene. The l isomer is almost devoid of analgesic activity; the compound does, however, show useful antitussive activity and is named levopropoxyphene.
References
References
- Reference.MD: [http://www.reference.md/files/C084/mC084813.html Propoxyphene napsylate]
- Lutje Spelberg. (2003). "Enantioselective biocatalytic conversions of epoxides". Rijksuniversiteit Groningen.
- (October 10, 1988). "Dextromethorphan binding sites in the guinea pig brain.". Cellular and Molecular Neurobiology.
- Chenier, Philip J. (2002) ''Survey of Industrial Chemistry''. Springer. {{ISBN. 0306472465. p. 455.
- (1953). "Analgesics: Esters of 4-Dialkylamino-1,2-diphenyl-2-butanols". Journal of the American Chemical Society.
This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.
Ask Mako anything about Levopropoxyphene — get instant answers, deeper analysis, and related topics.
Research with MakoFree with your Surf account
Create a free account to save articles, ask Mako questions, and organize your research.
Sign up freeThis content may have been generated or modified by AI. CloudSurf Software LLC is not responsible for the accuracy, completeness, or reliability of AI-generated content. Always verify important information from primary sources.
Report