Direct Access to Functional 2-Azabicyclo[2.1.1]hexanes via Hydrodearomative [2π + 2σ] Cycloaddition of Aza-arenes

Jian Yang,^[a] Bo-Xuan Yao,^[b] Huan-Feng Jiang,^[a] Shao-Fei Ni,*^[b] Pierre H. Dixneuf,^[c] and Min Zhang*^[a]

Converting planar six-membered aza-arenes into C(sp³)-rich three-dimensional (3D) scaffolds is a promising way to obtain isosteric mimetics of numerous functional products, but it remains to date a formidable challenge due to the high thermodynamic stability and dynamic inertness as well as the selectivity control. Here, by applying a novel non-noble bimetallic Mn/Fe catalyst system, we report, for the first time, an approach for direct construction of functional 3D 2-azabicyclo[2.1.1]hexanes via a hydrodearomatization (HDA) of the aza-arenes and [2π + 2σ] cycloaddition cascade. Mechanistic investigations reveal that the triplet state of Fe(II) facilitates the activation of both aza-arenes and bicyclo[1.1.0]butanes (BCBs). The mild reduction nature of manganese catalysis and the steric effects of Fe(II) coordination result in an 1,4-hydrodearomatization, and the imine species derived from the isomerization of 1,4-hydrogenated aza-arenes are then effectively trapped by the polarized BCBs, thus suppressing the thermodynamically favorable over-hydrogenation of aza-arenes into cyclic amine by-products. Given the features of good substrate and functionality compatibility, high step and atom efficiency, and diversified product post-transformations, the developed chemistry offers a practical platform to access various functional molecules.