The synthesis of benzimidazole 1 using a liquid phase approach is described
. Aromatic substitution of immobilized o-fluoronitrobenzene 2 with various
amines to o-nitroaniline derivatives 3 is carried out in methylene chloride
. Reduction of the aromatic nitro group, followed by subsequent cyclization
/elimination gives the benzimidazole skeleton. The crude library members ob
tained are of high yields and chemical purities after cleavage.