Abstract
An efficient synthesis of the 5-HT2C receptor agonist Org 37684 is presented. The synthesis utilises the regioselective demethylation of an arylether as the key step.
ACKNOWLEDGMENTS
We thank Dr. Ken Heatherington, Dr. Peter Clayton and Dr. Graeme Harden for performing the analysis on compounds 4 to 12. We also thank Dr. Ian Cliffe for helpful suggestions whilst preparing this manuscript and acknowledge the work of Mrs. Lyn Heaney in typing this paper.