Reaction of pentafluoropyridine with nucleophilic heteroaromatics such as 4‐(dimethylamino)pyridine, 4‐(pyrrolidin‐1‐yl)pyridine, 4‐(morpholin‐4‐yl)pyridine, 4‐aminopyridine, and 3,4‐diaminopyridine resulted in the formation of 4‐hetarenium substituted tetrafluoropyridines. The 4‐(dimethylamino)‐pyridinium derivative underwent substitution reactions with isopropanolate, isopropanethiolate, and benzylthiolate to F2,F3,O4,F5,F6‐ and O2,F3,O4,F5,F6‐pentasubstituted pyridines as well as their sulfur analogs. N‐Propylamine, isopropylamine, and piperidine formed 4‐amino‐N2,F3,F5,F6‐pentasubstituted pyridines in the presence of sodium amide as base, whereas morpholine gave the 4‐amino‐2,6‐bis‐morpholino‐substituted 3,5‐difluoropyridine. 19F, 15N, 13C, and 1H nmr spectrocopy was performed to elucidate the structures of the substitution products.