5-Fluoroimidazole-4-carboxylic acid ethyl eater was converted to the corres
ponding hydrazide. Oxidation of the hydrazide to the carbonyl azide and Cur
tius rearrangement in t-butyl alcohol produced 4-t-butyloxycarbonylamino-5-
fluoroimidazole. Dissolution of the t-butyl carbamate in 50% HBF4, in situ
diazotation of the resulting amine, and irradiation produced the target com
pound. (C) 2001 Elsevier Science B.V. All rights reserved.