Complementary Site-Selective Halogenation of Nitrogen-Containing (Hetero)Aromatics with Superacids

Abstract

Site-selective functionalization of arenes that is complementary to classical aromatic substitution reactions remains a long-standing quest in organic synthesis. Exploiting the generation of halenium ion through oxidative process and the protonation of the nitrogen containing function in HF/SbF₅ , the chlorination and iodination of classically inert Csp² -H bonds of aromatic amines occurs. Furthermore, the superacid-promoted (poly)protonation of the molecules acts as a protection, favoring the late-stage selective halogenation of natural alkaloids and active pharmaceutical ingredients.

Keywords: active pharmaceutical ingredients; halogenation; molecular diversity; protonation; reaction mechanisms.