Fragmentation patterns of novel dispirocyclopiperazinium dibromides with strong analgesic activity under electrospray ionization tandem mass spectrometry conditions

Rapid Commun Mass Spectrom. 2004;18(8):829-33. doi: 10.1002/rcm.1407.

Abstract

The fragmentation patterns of a series of dispirocyclopiperazinium dibromides with strong analgesic activity are analyzed by positive ion electrospray ionization mass spectrometry in conjunction with tandem mass spectrometry (ESI-MS(n)). Instead of the parent molecular ions, the fragment ions [M-Br](+) are detected as characteristic double peaks and usually the base peaks. Meanwhile, the fragment ions [M-2Br](2+) are unique for this series of diquaternary ammonium dibromides and show high intensity. Besides the common fragmentation patterns around the carbonyl group, elimination of hydrogen bromide from [M--Br](+) ions is another important pathway. Following the elimination, an interesting rearrangement takes place in the unsaturated spirocyclopiperazine and transforms it into a dihydropyrrole structure, whose fragmentations are similar to its precursor ion in the succeeding steps.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analgesics / analysis*
  • Bromides
  • Piperazines / analysis*
  • Spectrometry, Mass, Electrospray Ionization*
  • Spiro Compounds / analysis*

Substances

  • Analgesics
  • Bromides
  • Piperazines
  • Spiro Compounds