Hydrazine hydrate (1:1) → 3-Bromo-4-hydrazinyl-5-nitropyridine
反応式
[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([N+:9]([O-:11])=[O:10])[C:7]=1Cl.O.[NH2:13][NH2:14]>C(O)C>[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([N+:9]([O-:11])=[O:10])[C:7]=1[NH:13][NH2:14]参加物
4
実験手順
A solution of 3-bromo-4-chloro-5-nitro-pyridine (500 mg, 2.106 mmol), hydrazine hydrate (158.1 mg, 153.6 μL, 3.159 mmol) in ethanol (5.000 mL) was stirred at RT for 1 h. The bright yellow precipitate was filtered, washed with methanol and dried under vacuum to leave 3-bromo-4-hydrazinyl-5-nitropyridine (390 mg, 79.5%). MS (ES−) 232.8.
後処理
- filtrationThe bright yellow precipitate was filtered
- washwashed with methanol
- customdried under vacuum
出典と根拠
- ORDレコード
- ord-ebf75cf6720f41cf88fa846234f5a511
- 出典データセット
- uspto-grants-2016_05
- 特許番号
- US09340546B2
反応ノート
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