Back to Search Start Over

Synthesis of Montelukast (MK-0476) Metabolic Oxidation Products

Authors :
Marc Labelle
Laird A. Trimble
Rejean Ruel
Claude Dufresne
Michel Gallant
Yves Gareau
Source :
The Journal of Organic Chemistry. 61:8518-8525
Publication Year :
1996
Publisher :
American Chemical Society (ACS), 1996.

Abstract

We report the chemical synthesis of six oxidized derivatives of MK-0476 (Montelukast, L-706631), which have been key tools in the identification of its metabolites. We have prepared three diastereoisomeric pairs of potential oxidative metabolites of MK-0476, starting from the (S)-hydroxy ester 7 in 10 and five steps, and starting from MK-0476 itself in one step. The key benzylic hydroxyl of 1 and 2 was introduced by a bromination and saponification reaction sequence. In the case of the hydroxyl of 3 and 4, the key step was the addition of a hydroxymethyl carbanion equivalent on ketone 20. The two sulfoxide 5 and 6 were prepared by a direct oxidation of MK-0476 with m-chloroperbenzoic acid.

Details

ISSN :
15206904 and 00223263
Volume :
61
Database :
OpenAIRE
Journal :
The Journal of Organic Chemistry
Accession number :
edsair.doi...........aaaadf9d1c46c3d49506a29224e3d902
Full Text :
https://doi.org/10.1021/jo9615817