Synlett 2014; 25(2): 233-238
DOI: 10.1055/s-0033-1340151
letter
© Georg Thieme Verlag Stuttgart · New York

Nickel-Catalyzed Cross-Electrophile Coupling of 2-Chloropyridines with Alkyl Bromides

Daniel A. Everson
Department of Chemistry, University of Rochester, Rochester, NY 14627-0216, USA   Fax: +1(585)2760205   eMail: daniel.weix@rochester.edu
,
Joseph A. Buonomo
Department of Chemistry, University of Rochester, Rochester, NY 14627-0216, USA   Fax: +1(585)2760205   eMail: daniel.weix@rochester.edu
,
Daniel J. Weix*
Department of Chemistry, University of Rochester, Rochester, NY 14627-0216, USA   Fax: +1(585)2760205   eMail: daniel.weix@rochester.edu
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Publikationsverlauf

Received: 11. August 2013

Accepted after revision: 16. September 2013

Publikationsdatum:
05. November 2013 (online)


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Abstract

The synthesis of 2-alkylated pyridines by the nickel-catalyzed cross-coupling of two electrophiles, a 2-chloropyridine and an alkyl bromide, is described. Compared with our previously published conditions for aryl halides, this method uses a different, more rigid, bathophenanthroline ligand and is conducted at high concentration in N,N-dimethylformamide as solvent. The method displays promising functional group compatibility and the conditions are ­orthogonal to those for the Stille coupling.

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