反応式
[Cl:1][C:2]1[C:3](=[O:15])[N:4]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[N:5]=[CH:6][C:7]=1Cl.[CH3:16][NH:17][NH2:18].O>CO>[Cl:1][C:2]1[C:3](=[O:15])[N:4]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[N:5]=[CH:6][C:7]=1[N:17]([CH3:16])[NH2:18]参加物
5
実験手順
To a solution consisting of 22.9 grams of 4,5-dichloro-2-phenylpyridazin-3(2H)-one in 120 grams of methanol is added 20 grams of methylhydrazine. The reactants are heated to reflux for two hours, cooled and poured into one kilogram of water. The resulting precipitate is separated by filtration, washed with water and dried. The solid is crystallized from benzene and methanol to yield 4-chloro-2-phenyl-5-(1-methylhydrazino)-pyridazine-3(2H)-one (m.p. 128° to 130° C with decomposition).
後処理
- temperatureThe reactants are heated
- temperatureto reflux for two hours
- temperaturecooled
- customThe resulting precipitate is separated by filtration
- washwashed with water
- customdried
- customThe solid is crystallized from benzene and methanol
出典と根拠
- ORDレコード
- ord-1e39f32ecc734faaa13609b438039ac2
- 出典データセット
- uspto-grants-1977_01
- 特許番号
- US04002751
関連ノート
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