An Efficient One-Pot Process for 10-Bromo-8-chloro-5,6-dihydro-benzo[5,6]cyclohepta[1,2-b]pyridin-11-one, an Intermediate to SCH 66336

Author:

Fu Xiaoyong1,McAllister Timothy L.1,Shi Xiongwei1,Thiruvengadam T. K.1,Tann Chou-Hong1,Lee Junning1

Affiliation:

1. Synthetic Chemistry Department, Schering-Plough Research Institute, 1011 Morris Avenue, Union, New Jersey 07083, U.S.A.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference9 articles.

1. Farnesyl transferase inhibitors: a major breakthrough in anticancer therapy? Naples, 12 April 2002

2. Njoroge, F. G.; Girijavallabhan, V. M.Curr. Med.Chem.  Immunol., Endocr. Metab. Agents2001,1, 185−198. Liu, M.; Bryant, M. S.; Chen, J.; Lee, S.; Yaremko, B.; Lipari, P.; Malkowski, M.; Ferrari, E.; Nielsen, L.; Prioli, N.; Dell, J.; Sinha, D.; Syed, J.; Korfmacher, W. A.; Nomeir, A. A.; Lin, C.C.; Wang, L.; Taveras, A. G.; Doll, R. J.; Njoroge, F. G.; Mallams, A. K.; Remiszewski, S.; Catino, J. J.; Girijavallabhan, V. M.; Kirschmeier, P.; Bishop, W. R.Cancer Res.1998,58, 4947−4956.

3. Farnesyl Protein Transferase Inhibition: A Novel Approach to Anti-tumor

4. Highly Regioselective Nitration Reactions Provide a Versatile Method of Functionalizing Benzocycloheptapyridine Tricyclic Ring Systems:  Application toward Preparation of Nanomolar Inhibitors of Farnesyl Protein Transferase

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