Synthesis of highly functionalized 2,2′-bipyridines by cyclocondensation of β-ketoenamides - scope and limitations

The scope of a flexible route to unsymmetrically functionalized bipyridines is described. Starting from 1,3-diketones 1a-e, the corresponding beta-ketoenamines 2a-e were converted into different beta-ketoenamides 3a-g by N-acylation with 2-pyridinecarboxylic acid derivatives. These beta-ketoenamides were treated with a mixture of TMSOTf and Hunig's base to promote the cyclocondensation to 4-hydroxypyridine derivatives. Their immediate O-nonaflation employing nonafluorobutanesulfonyl fluoride provided the expected 4-nonafloxy-substituted bipyridine derivatives 5a-g in moderate to good overall yields. The bipyridyl nonaflates are excellent precursors for palladium-catalyzed reactions as demonstrated by representative Suzuki and Sonogashira couplings. Thus, a library of specifically substituted bipyridine derivatives was generated, showing the versatility of the simple 1,3-diketone-based approach to this important class of ligands.