Site-selective C5-H and -H alkylation of unprotected 8-aminoquinolines.

8-Aminoquinolines are the building blocks of many pharmaceutical compounds, which has motivated the scientific community to develop new ways to derivatize these compounds. In this work, we performed a site-selective C5-H and -H alkylation of 8-aminoquinolines using -quinone methides under extremely mild conditions. C5-H alkylation was performed using protecting group-free 8-aminoquinolines and in metal-free conditions. -H alkylations were also carried out under mild conditions. All corresponding alkylation products were obtained in high to excellent yields.