Site‐Selective Decarboxylative Direct Formylation of Nitrogen Heterocycles (Azaindoles, Indoles, Pyrroles) and Anilines Utilizing Glyoxylic Acid
Joydev K. Laha, Mandeep Kaur Hunjan, Tapas Maity, Amitava Hazra
Abstract
Abstract A new method for formylation of nitrogen heterocycles overcoming the limitations of classical approaches using a cheap feedstock formylating agent especially under mild and neutral conditions is the subject of this current investigation. This work describes direct formylation of nitrogen heterocycles (azaindoles, indoles, pyrroles) and anilines using glyoxylic acid as the formyl source and K 2 S 2 O 8 as the exclusive reagent. The key features include a general method for both C‐ and N‐formylation under neutral and mild reaction conditions. The application of the method is further demonstrated in the tandem synthesis of nitrogen heterocycles, pharmaceuticals, and a natural product. Unlike aroylation with arylglyoxylic acids, a previously unknown pathway for the direct formylation with glyoxylic acid in the presence of K 2 S 2 O 8 is now unveiled. magnified image