1-[(2'-(1H-tetrazole-5-yl)biphenyl-4-yl)merhyl]-4, 5, 6, 7-tetrahydroc
yclohept imidazole (KT3-671), which has been found to be a potent and
selective angiotesin II receptor antagonist, was synthesized in C-14-l
abelled form by using potassium[C-14]-cyanide. [C-14](KT3-671) 9 with
a specific activity of 1.74GBq/mmol was prepared in four steps in 29.8
% overall radiochemical yield from potassium[C-14]-cyanide.