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A mild method for the formation and in situ reaction of imidoyl chlorides: conversion of pyridine-1-oxides to 2-aminopyridine amides.
Manley, Peter J; Bilodeau, Mark T.
Afiliação
  • Manley PJ; Department of Medicinal Chemistry, Merck & Co., Inc., P.O. Box 4, West Point, Pennsylvania 19486, USA.
Org Lett ; 4(18): 3127-9, 2002 Sep 05.
Article em En | MEDLINE | ID: mdl-12201733
ABSTRACT
[reaction see text] A mild, practical, one-pot method for the generation of imidoyl chlorides and their subsequent in situ reaction with pyridine-1-oxides is described. The imidoyl chlorides were formed from the reaction of secondary amides with a stoichiometric amount of oxalyl chloride and 2,6-lutidine in CH(2)Cl(2) at 0 degrees C. Upon warming of the reaction mixture to room temperature in the presence of pyridine-1-oxides, a rapid conversion to 2-aminopyridine amides was observed in moderate to excellent isolated yields.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Amidas / Aminopiridinas Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2002 Tipo de documento: Article País de afiliação: Estados Unidos
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Amidas / Aminopiridinas Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2002 Tipo de documento: Article País de afiliação: Estados Unidos