One-Pot Synthesis of Bis(arylamino)pentiptycenes by TiCl4‑DABCO Assisted Reductive Amination of Pentiptycene Quinone

The previously eight-step synthesis of bis­(arylamino)­pentiptycenes (2) from pentiptycene quinone (1) can now be achieved in a single step with 18–90% yields through TiCl4-DABCO assisted reductive amination with anilines. Both the dual amination of 1 and the in situ reduction of quinone diimines are unprecedented. The π system of 2 can be further expanded, including the formation of bis­(diarylamino)­pentiptycenes. This work also provides mechanistic insights into the challenges encountered in the dual reductive amination of 1 with other amines.