Hydrazine hydrate (1:1) → 3-Chloro-6-hydrazinopyridazine
反応式
[Cl:1][C:2]1[N:3]=[N:4][C:5](Cl)=[CH:6][CH:7]=1.O.[NH2:10][NH2:11]>C(O)C>[Cl:1][C:2]1[N:3]=[N:4][C:5]([NH:10][NH2:11])=[CH:6][CH:7]=1参加物
4
実験手順
As shown in FIG. 5, a mixture of 40 g (0.27 mole) of 3,6-dichloropyridazine and 40 mL of 80% hydrazine hydrate in 80 mL of ethanol was refluxed for one hour. The reaction mixture was evaporated to dryness and the residue was recrystallized from benzene to give 39 g of 1-(6-chloropyridazin-3-yl)hydrazine (compound 1003) (see Takahayashi, J. Pharm. Soc. Japan 75:778-781, 1955).
後処理
- temperaturewas refluxed for one hour
- customThe reaction mixture was evaporated to dryness
- customthe residue was recrystallized from benzene
出典と根拠
- ORDレコード
- ord-6fb4034ab5794639bdf2ce1d1d5c13ae
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07728017B2
反応ノート
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