RAPID IDENTIFICATION OF ERGOT DERIVATIVES BY H-1-NMR SPECTROSCOPY

The 400 MHz H-1-NMR spectra of some therapeutically important ergot de rivatives (three bases, four protonated bases and four dihydroergoline salts) are analysed in terms of the low field chemical shift region ( above 5 ppm). common resonances of rings C and D (below 5 ppm) and C-8 substituent features. Attention is drawn to data of specific analytic al value. and a scheme for the rapid identification of members of this group of ergots proposed. Features which provide evidence of the solu te conformation of ring D, and isomerization to less active C-8 epimer s are also emphasized.