Isolation and characterisation of process-related impurities in rofecoxib

J Pharm Biomed Anal. 2002 Jun 20;29(1-2):355-60. doi: 10.1016/s0731-7085(02)00034-1.

Abstract

Two unknown impurities in rofecoxib bulk drug at levels below 0.1% were detected by a simple isocratic reverse phase high performance liquid chromatography (HPLC). These impurities were isolated from crude sample of rofecoxib using reverse phase preparative HPLC. (1)H, (13)C and Mass spectroscopic investigations revealed the structures of the impurities as 4-[4-(methylsulphonyl)phenyl]-3-phenyl-5-hydroxyfuran-2-one (I) and 4-[4-(methylsulphonyl)phenyl]-3-phenyl-2,5-furandione (II), respectively. These structures were further confirmed by prepared synthetic standards of the impurities. The tentative mechanism for the formation of these impurities was discussed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Inflammatory Agents, Non-Steroidal / analysis*
  • Chromatography, High Pressure Liquid / methods*
  • Drug Contamination*
  • Lactones / analysis*
  • Mass Spectrometry
  • Spectroscopy, Fourier Transform Infrared
  • Sulfones

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Lactones
  • Sulfones
  • rofecoxib