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Rapid Synthesis of Highly Substituted 1,6-Naphthyridines Via Heteroaryl Ditriflates.
Shimkin, Kirk W; Compton, Jordan S; Diccianni, Justin B; Waldo, Jesse P; Jones, William M; Krawczuk, Paul J; Rosano, Robert J.
Afiliación
  • Shimkin KW; Therapeutics Discovery, Janssen Pharmaceutical Research and Development, Spring House, Pennsylvania 19477, United States.
  • Compton JS; Therapeutics Discovery, Janssen Pharmaceutical Research and Development, Spring House, Pennsylvania 19477, United States.
  • Diccianni JB; Therapeutics Discovery, Janssen Pharmaceutical Research and Development, Spring House, Pennsylvania 19477, United States.
  • Waldo JP; Therapeutics Discovery, Janssen Pharmaceutical Research and Development, Spring House, Pennsylvania 19477, United States.
  • Jones WM; Therapeutics Discovery, Janssen Pharmaceutical Research and Development, Spring House, Pennsylvania 19477, United States.
  • Krawczuk PJ; Therapeutics Discovery, Janssen Pharmaceutical Research and Development, Spring House, Pennsylvania 19477, United States.
  • Rosano RJ; Therapeutics Discovery, Janssen Pharmaceutical Research and Development, Spring House, Pennsylvania 19477, United States.
J Org Chem ; 89(15): 10912-10918, 2024 Aug 02.
Article en En | MEDLINE | ID: mdl-39031089
ABSTRACT
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.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos