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Effective resolution of racemic pirlindole at the preparative scale
Authors:Pascal De Tullio  Attilio Ceccato  Jean-François Liégeois  Bernard Pirotte  Apostolos Felikidis  Monique Stachow  Philippe Hubert  Jacques Crommen  Joseph Géczy  Jacques Delarge
Affiliation:1. Department of Medicinal Chemistry, University of Liège, Liège, Belgium;2. Department of Drug Analysis, University of Liège, Liège, Belgium;3. Therabel Research, Brussels, Belgium
Abstract:Pirlindole, a racemic antidepressant drug, was recently resolved using the derivatization method coupled with preparative HPLC. In order to improve this technique, the use of amino acid derivatives as chiral derivatizing agents (CDA) was investigated. Among different residues, the (L)-phenylalanine methyl ester was found to be very effective to separate pirlindole enantiomers using a medium pressure liquid chromatographic (MPLC) method. This procedure is better adapted to preparative application than HPLC. Thus, several grams of the pirlindole antipodes were isolated and characterized. These two enantiomers permitted the study of the stereochemical influence at the pharmacological level. Chirality 11:261–266, 1999. © 1999 Wiley-Liss, Inc.
Keywords:pirlindole enantiomers  amino acid derivatives  derivatization  medium pressure liquid chromatography  chiral HPLC  RIMA  antidepressant drug
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