Literature DB >> 11711303

Synthetic study on novel immunosuppressant KF20444.

I Chujo1, Y Masuda, K Fujino, S Kato, T Ogasa, S Mohri, M Kasai.   

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.

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Year:  2001        PMID: 11711303     DOI: 10.1016/s0968-0896(01)00238-3

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  1 in total

1.  A Wittig-olefination-Claisen-rearrangement approach to the 3-methylquinoline-4-carbaldehyde synthesis.

Authors:  Mukund G Kulkarni; Mayur P Desai; Deekshaputra R Birhade; Yunus B Shaikh; Ajit N Dhatrak; Ramesh Gannimani
Journal:  Beilstein J Org Chem       Date:  2012-10-11       Impact factor: 2.883

  1 in total

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