Campos Kevin R, Journet Michel, Lee Sandra, Grabowski Edward J J, Tillyer Richard D
Department of Process Research, Merck Research Laboratories, P.O. Box 2000, RY800-B267, Rahway, New Jersey 07065-0900, USA.
J Org Chem. 2005 Jan 7;70(1):268-74. doi: 10.1021/jo048305+.
An asymmetric synthesis was developed for the production of a prostaglandin D(2) receptor antagonist for the treatment of allergic rhinitis. The stereogenic center was set using asymmetric allylic alkylation chemistry, and the core of the structure was constructed via Pd-catalyzed N-cyclization/Heck methodology. The synthesis relies on a late stage indoline oxidation which does not racemize the product.