Strategies for Access to Enantiomerically Pure Ecadotril, Dexecadotril and Fasidotril: A Review

Title: Strategies for Access to Enantiomerically Pure Ecadotril, Dexecadotril and Fasidotril: A Review

Volume: 2 Issue: 3

Author(s): Thierry Monteil, Denis Danvy, Miryam Sihel, Richard Leroux and Jean-Christophe Plaquevent

Affiliation:

Keywords: ecadotril, dexecadotril, fasidotril, neprilysin inhibitor

Abstract: Ecadotril and dexecadotril are powerful and selective inhibitors of neprilysin (NEP, EC 3.4.24.11) and are being developed as therapeutic agents, since they behave as prodrugs of the enantiomers of thiorphan. They exhibit different pharmaceutical profiles (intestinal antisecretatory action for the (R) enantiomer, i.e. dexecadotril, and cardiovascular activity for the (S) enantiomer, i.e. ecadotril). Fasidotril is a related compound which has special interest as an equipotent dual inhibitor of NEP and ACE (EC 3.4.15.1). This behavior confers on fasidotril powerful pharmaceutical properties in the cardiovascular field. This review deals with various synthetic approaches, either published or patented, for access to the enantiomerically pure or highly enriched forms of these drugs. Thus, different methods have been studied, which are taken from different methodologies of resolution procedures and asymmetric synthesis, namely : i- Synthesis from a chiron from the chiral pool ii- Chemical resolution of racemic precursors iii- Enzymatic resolution and desymmetrization of meso starting materials iv- Asymmetric synthesis, including enantioselective catalytic hydrogenation, alkaloid catalyzed asymmetric Michael additions, and diastereoselective alkylation of a chiral derivative. Some of these methods are used in industrial processes leading to the indicated compounds.

Cite this article as:

Monteil Thierry, Danvy Denis, Sihel Miryam, Leroux Richard and Plaquevent Jean-Christophe, Strategies for Access to Enantiomerically Pure Ecadotril, Dexecadotril and Fasidotril: A Review, Mini-Reviews in Medicinal Chemistry 2002; 2 (3) . https://dx.doi.org/10.2174/1389557023406133