C−H Methylation of Iminoamido Heterocycles with Sulfur Ylides**
Prithwish Ghosh, Na Yeon Kwon, Saegun Kim, Sangil Han, Suk Hun Lee, Won Gun An, Neeraj Kumar Mishra, Soo Bong Han, In Su Kim
Abstract
Abstract The direct methylation of N ‐heterocycles is an important transformation for the advancement of pharmaceuticals, agrochemicals, functional materials, and other chemical entities. Herein, the unprecedented C(sp 2 )‐H methylation of iminoamido heterocycles as nucleoside base analogues is described. Notably, trimethylsulfoxonium salt was employed as a methylating agent under aqueous conditions. A wide substrate scope and excellent level of functional‐group tolerance were attained. Moreover, this method can be readily applied to the site‐selective methylation of azauracil nucleosides. The feasibility of gram‐scale reactions and various transformations of the products highlight the synthetic potential of the developed method. Combined deuterium‐labeling experiments aided the elucidation of a plausible reaction mechanism.