Merck
CN
  • A mild method for the formation and in situ reaction of imidoyl chlorides: conversion of pyridine-1-oxides to 2-aminopyridine amides.

A mild method for the formation and in situ reaction of imidoyl chlorides: conversion of pyridine-1-oxides to 2-aminopyridine amides.

Organic letters (2002-08-31)
Peter J Manley, Mark T Bilodeau
摘要

[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.

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Sigma-Aldrich
草酰氯, ReagentPlus®, ≥99%
Sigma-Aldrich
草酰氯, reagent grade, 98%
Sigma-Aldrich
草酰氯 溶液, 2.0 M in methylene chloride