Synthesis 1992; 1992(6): 528-530
DOI: 10.1055/s-1992-26153
short paper
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

The Synthesis of Thienopyridines from ortho-Halogenated Pyridine Derivatives

D. H. Bremner* , A. D. Dunn, K. A. Wilson
  • *Dundee Institute of Technology, Department of Molecular and Life Sciences, Bell Street, Dundee DD1 1HG, Scotland
Further Information

Publication History

Publication Date:
17 September 2002 (online)

The synthesis of 2- and 4-chloro-3-cyanomethylpyridine, 3-bromo-2-cyanomethylpyridine and 3-bromo-4-cyanomethylpyridine containing methylene groups activated by the nitrile functionality is reported. Reaction of these compounds with sodium hydride and carbon disulfide, followed by iodomethane gives the corresponding thienopyridines.

    >