反応式
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([CH:10]2[CH2:15][CH2:14][NH:13][CH2:12][CH2:11]2)=[CH:6][CH:5]=1)([O-])=O.[C:16](=O)([O:22]C(C)(C)C)[O:17][C:18]([CH3:21])([CH3:20])[CH3:19].C([O-])(O)=O.[Na+]>C(Cl)Cl.CN(C)C1C=CN=CC=1>[NH2:1][C:4]1[CH:9]=[CH:8][C:7]([CH:10]2[CH2:15][CH2:14][N:13]([C:16]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:22])[CH2:12][CH2:11]2)=[CH:6][CH:5]=1参加物
6
実験手順
To a solution of 4-(4-nitrophenyl)piperidine (412 mg, 2 mmol) in CH2Cl2 (100 mL) was added di-tert-butyl carbonate (480 mg, 2.2 mmol) and N,N-dimethylpyridin-4-amine (50 mg, 0.4 mmol). The mixture was stirred for 20 h at room temperature. The mixture was added saturated NaHCO3 (100 mL). The organic layer was separated and aqueous was extracted with CH2Cl2 (50 mL×2). The combined organic solution was dried and concentrated in vacuo. The residue was dissolved in MeOH and bubbled with Ar for 2 min. before adding 10% Pd—C. The hydrogenation was finished in 4 h. The catalyst was removed by filtration and solvent was removed in vacuo to afford title compound (460 mg, 83%) as white solid.
後処理
- customThe organic layer was separated
- extractionaqueous was extracted with CH2Cl2 (50 mL×2)
- customThe combined organic solution was dried
- concentrationconcentrated in vacuo
- dissolutionThe residue was dissolved in MeOH
- custombubbled with Ar for 2 min.
- additionbefore adding 10% Pd—C
- waitThe hydrogenation was finished in 4 h
- customThe catalyst was removed by filtration and solvent
- customwas removed in vacuo
出典と根拠
- ORDレコード
- ord-85d34c0e64314517801fff44d77b368f
- 出典データセット
- uspto-grants-2009_05
- 特許番号
- US07528143B2
関連ノート
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