反応式
[N+:1]([C:4]1[CH:9]=[CH:8][N:7]=[C:6]([N:10]2[CH2:14][CH2:13][CH2:12][CH2:11]2)[CH:5]=1)([O-])=O.C(Cl)Cl>CO.[C].[Pd]>[N:10]1([C:6]2[CH:5]=[C:4]([NH2:1])[CH:9]=[CH:8][N:7]=2)[CH2:11][CH2:12][CH2:13][CH2:14]1参加物
5
実験手順
4-Nitro-2-(pyrrolidin-1-yl)pyridine (560 mg, 2.90 mmol) was dissolved in methanol (21 mL) and methylene chloride (8.3 mL) and the solution was added with palladium carbon (50% aqueous, 560 mg), followed by stirring at room temperature for 1 hour under hydrogen atmosphere. After filtering off the insoluble matter of the reaction mixture, the solvent was evaporated under reduced pressure to obtain 2-(pyrrolidin-1-yl)pyridin-4-ylamine (474 mg, 91%).
後処理
- filtrationAfter filtering off the insoluble matter of the reaction mixture
- customthe solvent was evaporated under reduced pressure
出典と根拠
- ORDレコード
- ord-10882eee6a864c68b33dae3554d254a7
- 出典データセット
- uspto-grants-2011_03
- 特許番号
- US07906522B2
関連ノート
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