Hydrazine → Ethyl 2-hydrazinylnicotinate
反応式
Cl[C:2]1[N:12]=[CH:11][CH:10]=[CH:9][C:3]=1[C:4]([O:6][CH2:7][CH3:8])=[O:5].[NH2:13][NH2:14]>O1CCOCC1>[CH2:7]([O:6][C:4](=[O:5])[C:3]1[CH:9]=[CH:10][CH:11]=[N:12][C:2]=1[NH:13][NH2:14])[CH3:8]参加物
反応条件
- 温度
- 60 °C
実験手順
A solution of ethyl 2-chloronicotinate (10.0 g, 53.9 mmol) and anhydrous hydrazine (2.04 g, 63.8 mmol) in anhydrous 1,4-dioxane (200 mL) was stirred at 60° C. for 2 h. Analysis by LC/MS indicated the starting material was not consumed. Additional amount hydrazine (2.04 g, 63.8 mmol) was added and the reaction mixture was stirred at 60° C. overnight. After cooling to room temperature, the reaction mixture was concentrated in vacuo. The obtained residue was triturated with MeOH (35 mL), the insoluble white solid was removed by filtration and discarded. The methanol solution was concentrated in vacuo to yield a fluffy yellow solid which was triturated in diethylether to yield the title compound as an orange solid (5.4 g, 55%). HPLC/MS (Method D): retention time=1.46 min, [M+H]+=182.3.
後処理
- customwas not consumed
- temperatureAfter cooling to room temperature
- concentrationthe reaction mixture was concentrated in vacuo
- customThe obtained residue was triturated with MeOH (35 mL)
- customthe insoluble white solid was removed by filtration
- concentrationThe methanol solution was concentrated in vacuo
- customto yield a fluffy yellow solid which
- customwas triturated in diethylether
出典と根拠
- ORDレコード
- ord-cecee5ee1fc8460fb19765fa07c64279
- 出典データセット
- uspto-grants-2012_12
- 特許番号
- US08324241B2
反応ノート
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