Five‐Membered Nitrogen Heterocycles Synthesis through 1,3‐Dipolar Cycloaddition of Non‐Stabilized Azomethine Ylides with 2‐Pyridone Heteroaromatic Systems as Dipolarophiles

We report an efficient 1,3‐dipolar cycloaddition involving non‐stabilized electron‐rich azomethine ylides and diversely substituted 2‐pyridones bearing two potential C=C dipolarophilic sites. The 1,3‐dipoles were prepared in situ under TFA catalysis and cycloadditions were studied according to the nature of the pyridones and position of the various substituents. These reactions occur under mild conditions, and lead to the expected cycloadducts in good yields and full control of the regioselectivity. Furthermore, mono‐ or biscycloadditions were performed, leading to the formation of polycyclic scaffolds bearing biologically relevant pyrrolidine rings, prevalent in natural products. The diastereoselectivity of the second cycloaddition was fully controlled by the first addition, leading to heterocycles with a trans relative stereochemistry of the two generated rings in the final tricyclo‐adduct. A series of highly efficient 1,3‐dipolar cycloadditions of non‐stabilized azomethine ylides with diversely substituted 2‐pyridone systems, bearing two potential C=C dipolarophilic sites was reported. The TFA‐catalyzed cycloadditions involving the in situ prepared electron‐rich 1,3‐dipole are studied according to the nature of pyridone substituents. These reactions occur in mild conditions, good yields, and show a full control of the regioselectivity.