Rapid Synthesis of Highly Substituted 1,6-Naphthyridines Via Heteroaryl Ditriflates

We report the discovery of a convenient and efficient method for the synthesis of highly substituted 1,6-naphthyridines. A tandem nitrile hydration/cyclization procedure was developed to access 1,6-naphthyridine-5,7-diones under mild conditions. Subsequently, we have found that ditriflation of these...

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Veröffentlicht in:Journal of organic chemistry 2024-08, Vol.89 (15), p.10912-10918
Hauptverfasser: Shimkin, Kirk W., Compton, Jordan S., Diccianni, Justin B., Waldo, Jesse P., Jones, William M., Krawczuk, Paul J., Rosano, Robert J.
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Sprache:eng
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Zusammenfassung:We report the discovery of a convenient and efficient method for the synthesis of highly substituted 1,6-naphthyridines. A tandem nitrile hydration/cyclization procedure was developed to access 1,6-naphthyridine-5,7-diones under mild conditions. Subsequently, we have found that ditriflation of these intermediates provides 1,6-naphthyridine-5,7-ditriflates which are bench-stable but highly reactive intermediates that can be engaged in one-pot difunctionalization reactions leading to diverse drug-like products in rapid fashion.
ISSN:0022-3263
1520-6904
1520-6904
DOI:10.1021/acs.joc.4c01248