Premium
Studies on pyrazines. 13 . Chlorination of 1‐hydroxy‐2(1 H )‐pyrazinones with phosphoryl chloride. Formation of 2,5‐dichloro‐3‐phenylpyrazine from 1‐hydroxy‐3‐phenyl‐2(1 H )‐pyrazinone
Author(s) -
Sato Nobuhiro
Publication year - 1986
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570230130
Subject(s) - chemistry , reagent , phosphoryl chloride , chloride , medicinal chemistry , stereochemistry , organic chemistry
The chlorination of 1‐hydroxy‐3‐phenyl‐2(1 H )‐pyrazinone with phosphoryl chloride proceeded to 5‐chloro‐3‐phenyl‐2( H )‐pyrazinone or 2,5‐dichloro‐3‐phenylpyrazine on heating to elevated temperatures. To define the mechanism of the novel formation, reactions of the parent or methyl‐substituted 1‐hydroxy‐2(1 H )‐pyraz‐inones with the same reagent were investigated.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom