Regioselective Halogenations and Subsequent Suzuki−Miyaura Coupling onto Bicyclic 2-Pyridones

A selective synthesis of 6-bromo-8-iodo dihydro thiazolo ring-fused 2-pyridones is described. These halogenated 2-pyridones are selectively arylated by sequential Suzuki−Miyaura couplings. This approach can advantageously be used to synthesize focused libraries of substituted ring-fused 2-pyridones,...

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Veröffentlicht in:Journal of organic chemistry 2010-02, Vol.75 (3), p.972-975
Hauptverfasser: Bengtsson, Christoffer, Almqvist, Fredrik
Format: Artikel
Sprache:eng
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Zusammenfassung:A selective synthesis of 6-bromo-8-iodo dihydro thiazolo ring-fused 2-pyridones is described. These halogenated 2-pyridones are selectively arylated by sequential Suzuki−Miyaura couplings. This approach can advantageously be used to synthesize focused libraries of substituted ring-fused 2-pyridones, a class of compounds with novel antibacterial properties.
ISSN:0022-3263
1520-6904
1520-6904
DOI:10.1021/jo902458g