The electron impact mass spectra of new 5-acetyl-4-aryl-6-methyl-2(1H)pyrid
ones have been studied. A dominant peak in all the spectra is due to cleava
ge of the CO-NH bond of the amido group with charge retention on the carbon
yl group. This fragmentation is followed by a hydrogen rearrangement to the
nitrogen atom forming ketene intermediates; this pathway leads to a highly
stabilized ion which constitutes the base peak in the spectra in most of t
he compounds studied. Copyright (C) 1999 John Wiley & Sons, Ltd.