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Reaction of 1‐chloromethyl‐4,5‐dichloropyridazin‐6‐one
Author(s) -
Chung HyunA,
Kang YoungJin,
Yoon YongJin
Publication year - 1998
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.5570350603
Subject(s) - chemistry , sodium methoxide , sodium azide , nucleophile , phenol , azide , sodium , medicinal chemistry , organic chemistry , methanol , catalysis
Reaction of 1‐chloromethyl‐4,5‐dichloropyridazin‐6‐one with some nucleophiles such as sodium methoxide, sodium azide, 2‐mercaptopyrimidine and phenol gave 2, 3, 4, 7, 8 and 10 . 5‐Chloro‐4‐phenoxypyridazin‐6‐one ( 10 ) was also synthesized from 8 through 9.
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