The long-range scalar coupling constant between proton and fluorine nuclei, J , is observed to be larger than J in the pyrimidinyl moiety of voriconazole. A set of smaller molecules is chosen (fluorobenzene, N-methyl-2-fluoropyridine, N-methyl-3-fluoropyridine, 3-fluoropyridine, 5-pyrimidine, and 2-fluoropyridine) to evaluate the influence of the nitrogen atom in the experimental J values. Spectral aliased pure shift heteronuclear single quantum coherence spectroscopy (SAPS-HSQC) is applied to determine the relative sign between the J and J scalar couplings. Theoretical calculations show that the J and J coupling constants can be described mainly by a Fermi contact (FC) transmission mechanism. A decomposition analysis of J in terms of localized molecular orbital (LMO) contributions allows us to determine that the interaction involving the nitrogen lone pair (LPN) is the main reason for the larger J compared to J . Our analysis indicates that delocalization of LPN has a positive contribution to the long-range coupling, while a negative one is observed for J .