Pharmaceutical Bulletin
Online ISSN : 1881-1345
Print ISSN : 0369-9471
ISSN-L : 0369-9471
Synthesis of Pyridazine Derivatives. VIII. Nucleophilic Substitution of 3, 6-Dichloro-4-methylpyridazine.
高林 昇
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ジャーナル フリー

1957 年 5 巻 3 号 p. 229-234

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In the reaction of 3, 6-dichloro-4-methylpyridazine (I) with hydrazine hydrate, ammonia, sodium hydroxide, sodium methoxide, or potassium hydrogen sulfide, monosubstituted compounds were obtained. The position of methyl group in those compounds and the relationship among them were cleared up. Examination was also made on whether substitution in (I) occurred in 3- or in 6-position according to the change of conditions. 6-Chloro-8-methyl-s-triazolo [4, 3-b] pyridazine and 6-chloro-7-methyl-s-triazolo [4, 3-b]-pyridazine were prepared from 3-hydrazino-4-methyl-6-chloropyridazine and 3-hydrazino-5-methyl-6-chloropyridazine, and were derived to their 6-hydrazino derivatives.
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© The Pharmaceutical Society of Japan
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