An effective one-pot synthesis of quinolines bearing diverse C3-piperazinyl functions was developed by using a modified Friedländer's protocol. The method not only enables the synthesis of our early reported c-Met inhibitor on a large scale, but also provides a way to generate novel multi-substituted quinolines for further structure-activity relationship (SAR) study.
|Original language||English (US)|
|Number of pages||4|
|Journal||Organic and Biomolecular Chemistry|
|State||Published - Sep 7 2011|
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Organic Chemistry