Computational Studies of Reactions of 1,2,4,5-Tetrazines with Enamines in MeOH and HFIP

The reaction between 1,2,4,5-tetrazines and alkenes in polar solvents proceeds through a Diels–Alder cycloaddition along the C–C axis (C3/C6 cycloaddition) of the tetrazine, followed by dinitrogen loss. By contrast, the reactions of 1,2,4,5-tetrazines with enamines in hexafluoroisopropanol (HFIP) give 1,2,4-triazine products stemming from a formal Diels–Alder addition across the N–N axis (N1/N4 cycloaddition). We explored the mechanism of this interesting solvent effect through DFT calculations in detail and revealed a novel reaction pathway characterized by C–N bond formation, deprotonation, and a 3,3-sigmatropic rearrangement. The participation of an HFIP molecule was found to be crucial to the N1/N4 selectivity over C3/C6 due to the more favored initial C–N bond formation than C–C bond formation.