4.0 Article

Preparation of (-)-(R)-2-(2,3,4,5,6-pentafluorophenoxy)-2-(phenyl-d5)acetic acid: an efficient 1H NMR chiral solvating agent for direct enantiomeric purity evaluation of quinoline-containing antimalarial drugs

Journal

TETRAHEDRON-ASYMMETRY
Volume 25, Issue 24, Pages 1605-1611

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetasy.2014.11.007

Keywords

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Funding

  1. Ministero dell'Istruzione, dell'Universita e della Ricerca [MIUR 2010FPTBSH _002]
  2. Assessorato alla Qualita dell'Ambiente (Regione Puglia)

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The title compound was prepared as a racemate from (+/-)-mandelic acid-d(5) in one step. The corresponding (-)-(R)-enantiomer (98% ee) was obtained by resolution with (-)-(R)-1-phenylethylamine and evaluated as a chiral solvating agent (CSA) for direct H-1 NMR enantiomeric excess determination of mefloquine (Lariam (R), chloroquine (Chloroquine Bayer (R)), and hydroxychloroquine (Plaquenil (R)) enantiomers. The displayed non-equivalence was high for signals in the aromatic region of all three antimalarials. Thus, the mandelic acid derivative described herein may be considered as the first efficient CSA 'invisible' in the aromatic region, useful for direct H-1 NMR ee value determination of chiral quinoline-containing antimalarial drugs. (C) 2014 Elsevier Ltd. All rights reserved.

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