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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.

Authors :
Manley PJ
Bilodeau MT
Source :
Organic letters [Org Lett] 2002 Sep 05; Vol. 4 (18), pp. 3127-9.
Publication Year :
2002

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.

Details

Language :
English
ISSN :
1523-7060
Volume :
4
Issue :
18
Database :
MEDLINE
Journal :
Organic letters
Publication Type :
Academic Journal
Accession number :
12201733
Full Text :
https://doi.org/10.1021/ol0264556