Synfacts 2006(4): 0301-0301  
DOI: 10.1055/s-2006-932029
Synthesis of Natural Products and Potential Drugs
© Georg Thieme Verlag Stuttgart · New York

Synthesis of a Neuropeptide Y Antagonist

Contributor(s): Philip Kocienski
T. Iida*, H. Satoh, K. Maeda, Y. Yamamoto, K. Asakawa, N. Sawada, T. Wada, C. Kadowski, T. Itoh, T. Mase, S. A. Weissman*, D. Tschaen, S. Krska, R. P. Volante
Banyu Pharmaceuticals, Okazaki, Japan and Merck & Co., Rahway, USA
Further Information

Publication History

Publication Date:
24 March 2006 (online)

Significance

Compound G is under clinical trials for the treatment of obesity owing to its antagonism of neuropeptide Y (NPY), an important regulator of feeding behavior. A major challenge in the synthesis of G was the control of the relative ste­reochemistry between the spirocyclic center and the carboxyl appendage in intermediate C. The problems here were (a) that the addition to the ketone B was not particularly stereoselective and (b) that the equilibration was useless because the thermodynamic product was the wrong cis isomer.