Synthesis 2007(17): 2711-2719  
DOI: 10.1055/s-2007-983824
PAPER
© Georg Thieme Verlag Stuttgart · New York

Synthesis of Amino-Functionalized 2,2′-Bipyridines

Marko Hapkeb, Holger Staatsa, Ivonne Wallmanna, Arne Lützen*a
a Kekulé-Institute of Organic Chemistry and Biochemistry, University of Bonn, Gerhard-Domagk-Straße 1, 53121 Bonn, Germany
b Leibniz-Institut für Katalyse e.V., Universität Rostock, Albert-Einstein-Straße 29a, 18059 Rostock, Germany
Fax: +49(228)739608; e-Mail: arne.luetzen@uni-bonn.de;
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Publikationsverlauf

Received 25 May 2007
Publikationsdatum:
30. Juli 2007 (online)

Abstract

Amino-functionalized 2,2′-bipyridines are versatile building blocks for the synthesis of sophisticated chelating ligands with the 2,2′-bipyridine core. The 4-, 5-, and 6-substituted 2-chloro- and 2-bromopyridine building blocks were prepared and coupled to symmetrically and non-symmetrically diamino-functionalized compounds by homo- and cross-coupling procedures. Further transformations were carried out to demonstrate the synthetic versatility of these compounds and the employed procedures.