1961Recueil des Travaux Chimiques des Pays-BasRequires access

The action of p‐toluenesulphonyl chloride on pyridine‐n‐oxide (III)

H. J. den Hertog, D. J. Buurman, Pierre Villiers

Open publisher page 10 citations

Abstract

Abstract The reaction mixture formed during the heating of pyridine‐N‐oxide with p‐toluenesulphonyl chloride contains, together with pyridine, 2,3′‐dipyridyl ether, 3‐pyridyl p‐toluenesulphonate and N‐(2Prime;‐pyridyl)‐pyridone‐2 two chloro compounds, viz. N‐(2′‐pyridyl)‐5‐chloro‐pyridone‐2, which is the chief product, and N‐(2′‐pyridyl)‐3‐chloro‐pyridone‐2. In this connection the formation of brominated derivatives of N‐(2′‐pyridyl)‐pyridone‐2 during the reaction of pyridine‐N‐oxide and 2‐bromopyridine, as described by Ramirez and von Ostwalden is discussed.

About this research paper

What this paper is about

Abstract The reaction mixture formed during the heating of pyridine‐N‐oxide with p‐toluenesulphonyl chloride contains, together with pyridine, 2,3′‐dipyridyl ether, 3‐pyridyl p‐toluenesulphonate and N‐(2Prime;‐pyridyl)‐pyridone‐2 two chloro compounds, viz. N‐(2′‐pyridyl)‐5‐chloro‐pyridone‐2, which is the chief product, and N‐(2′‐pyridyl)‐3‐chloro‐pyridone‐2. In this connection the formation of brominated derivatives of N‐(2′‐pyridyl)‐pyridone‐2 during the reaction of pyridine‐N‐oxide and 2‐bromopyridine, as described by Ramirez and von Ostwalden is discussed.

Why it matters

OpenAlex reports 10 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Abstract The reaction mixture formed during the heating of pyridine‐N‐oxide with p‐toluenesulphonyl chloride contains, together with pyridine, 2,3′‐dipyridyl ether, 3‐pyridyl p‐toluenesulphonate and N‐(2Prime;‐pyridyl)‐pyridone‐2 two chloro compounds, viz. N‐(2′‐pyridyl)‐5‐chloro‐pyridone‐2, which is the chief product, and N‐(2′‐pyridyl)‐3‐chloro‐pyridone‐2. In this connection the formation of brominated derivatives of N‐(2′‐pyridyl)‐pyridone‐2 during the reaction of pyridine‐N‐oxide and 2‐bromopyridine, as described by Ramirez and von Ostwalden is discussed.

Key concepts: Pyridine, Pyridine-N-oxide, Chemistry, Ether, Medicinal chemistry, Chloride, Oxide, Organic chemistry

Related papers

Back to paper searchBrowse research topicsOriginal source
The action of p‐toluenesulphonyl chloride on pyridine‐n‐oxide (III) — Research Paper | ScholarLens