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Synthetic study on novel immunosuppressant KF20444
1Sakai Research Laboratories, Kyowa Hakko Kogyo Co., Ltd., 1-1-53, Takasu-cho, Sakai, Osaka 590-8554, Japan. iwao.chujo@kyowa.co.jp
Bioorganic & Medicinal Chemistry
|November 17, 2001
Abstract:
The two new synthetic routes to 6,7-dihydro-10-fluoro-3-(2-fluorophenyl)-5H- benzo[6,7]cyclohepta[1,2-b]-quinoline-8-carboxylic acid (1), a novel immunosuppressant KF20444, are described. The seven-membered ring construction from 2-[4-(2-fluorophenyl)phenyl]-3-(2-carboxyethyl)-4-chloromethyl-6-fluoroquinoline (17c) was achieved by intramolecular Friedel-Crafts reaction under acidic conditions as the key step. Subsequently, the oxidation of 4-chloromethyl group followed by reduction of carbonyl group on the seven-membered ring afforded 1. This route provides a new method for the synthesis of 1.