Bicyclic Isosteres of Pyridine/Piperidine: From Synthesis to Applications
Oleksandr Stashkevych, Volodymyr Kokhalskyi, Yevhenii Mynak, Vadym V. Levterov, Oleh Shablykin, Iryna Pishel, Pavel K. Mykhailiuk
Abstract
Abstract 2‐Azabicyclo[2.2.2]octanes have been designed, synthesized, and validated biologically as isosteres of piperidine/pyridine. The key reaction step was the cyclization of cyclic alkenyl amines with the KO t Bu/I 2 /CO 2 combination. The method proved to be scalable (up to 20 g) and general: it was also applied for the synthesis of 2‐azabicyclo[2.1.1]hexanes, 2‐azabicyclo[3.1.1]heptanes, 2‐azabicyclo[2.2.1]heptanes, 7‐azabicyclo[2.2.1]heptanes, and 6‐azabicyclo[3.2.1]octanes. Finally, combined with the nitrogen deletion tactic, this method also opened a practical way toward the previously hardly accessible 1,2‐disubstituted bicyclo[1.1.1]pentanes—saturated analogues of ortho ‐benzenes.