Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Studies on Pyridazines. XVIII. Cyanation of 3, 3'-Bipyridazines and Their N-Oxides via Their Quaternary Salts
HIROSHI IGETATAKASHI TSUCHIYACHISATO OKUDAHIDEHARU YOKOGAWA
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1971 Volume 19 Issue 7 Pages 1297-1300

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Abstract
The reaction of quaternary salts of 3, 3'-bipyridazines and their N-oxides with cyanide ion was carried out. 3, 3'-Bipyridazine 1, 1'-dioxides (I, II) gave the dihydro compounds having cyano groups at α-positions to the N-oxide groups (IV, V). The bipyridazines without N-oxide groups (VII, VIII) afforded the dihydro compounds having cyano groups at γ-positions to the N-CH3 groups (X, XI). And 6, 6'-dimethoxy-3, 3'-bipyridazine (IX) afforded 1, 1'-dimethyl-3, 3'-bipyridazine-6, 6'(1H, 1'H)-dione (XII). As for the 2, 2'-dioxide (III), the compound composed of both the dihydro type ring and the aromatic ring formed by the elimination of the methoxy group (VI), was obtained.
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© The Pharmaceutical Society of Japan
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