Synthesis, chromatographic resolution and chiroptical properties of carboxyibuprofen stereoisomers: major metabolites of ibuprofen in man

Chirality. 1997;9(1):75-87. doi: 10.1002/(SICI)1520-636X(1997)9:1<75::AID-CHIR14>3.0.CO;2-N.

Abstract

The chromatographic resolution of the four stereoisomers of carboxy-ibuprofen, a major metabolite of ibuprofen in man, was achieved using a Chiralpak AD chiral stationary phase (CSP) (J.T. Baker, Milton, Keynes, UK). The elution order of the stereoisomers was determined to be 2'S,2R;2'R,2R;2'R,2S;2'S,2S by a combination of stereoselective synthesis of diastereoisomeric mixtures and analysis of the two diastereoisomers isolated from human urine following the administration of (S)-ibuprofen. The individual stereoisomers were isolated by semipreparative chiral phase chromatography and characterized by circular dichroism spectroscopy.

MeSH terms

  • Anti-Inflammatory Agents, Non-Steroidal / metabolism*
  • Chromatography, High Pressure Liquid / methods
  • Circular Dichroism
  • Humans
  • Ibuprofen / analogs & derivatives
  • Ibuprofen / chemical synthesis
  • Ibuprofen / chemistry*
  • Ibuprofen / isolation & purification
  • Ibuprofen / metabolism*
  • Magnetic Resonance Spectroscopy
  • Optics and Photonics
  • Oxidation-Reduction
  • Stereoisomerism

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Ibuprofen