Sodium cyanoborohydride → 6-[4-(3-Propyl-piperidin-1-ylmethyl)-phenoxy]-nicotinamide
反応式
[CH3:1][O:2][C:3]1[CH:18]=[CH:17][C:6]([CH2:7][N:8]2[CH2:13][CH2:12][CH2:11][CH:10]([CH2:14][CH2:15][CH3:16])[CH2:9]2)=[CH:5][CH:4]=1.[H][H].C(C1C=CC(OC2[CH:35]=[CH:34][C:31]([C:32]#[N:33])=[CH:30][N:29]=2)=CC=1)=O.[BH3-]C#N.[Na+].CC(O)=[O:44].CO>[OH-].[OH-].[Pd+2].C(O)C>[CH2:14]([CH:10]1[CH2:11][CH2:12][CH2:13][N:8]([CH2:7][C:6]2[CH:5]=[CH:4][C:3]([O:2][C:1]3[CH:35]=[CH:34][C:31]([C:32]([NH2:33])=[O:44])=[CH:30][N:29]=3)=[CH:18][CH:17]=2)[CH2:9]1)[CH2:15][CH3:16]参加物
反応物 5
生成物 1
試薬・触媒・溶媒 2
実験手順
Combine 1-(4-Methoxy-benzyl)-3-propyl-piperidine (105.2 mg, 0.43 mmol), Ethanol (50 mL), 20% Pd(OH)2/C (75.0 mg), and a Hydrogen at 30° C. under 50-60 psi for 12 hours on a Parr shaker. Filter the reaction mixture and then add 5% AcOH/MeOH (3 mL), 6-(4-Formyl-phenoxy)-nicotinonitrile (Intermediate 51) (40.0 mg, 0.31 mmol), and NaCNBH3 (83.7 mg, 0.34 mmol). Stir the reaction at room temperature for 72 hours and then concentrate the reaction mixture under reduced pressure. Add the reaction mixture to an SCX Column (2 g), wash with methanol, and elute with 1N NH3 MeOH. Concentrate under reduced pressure and flash chromatograph using 3% 1N NH3 MeOH in CH2Cl2 to give 19.8 mg (18% yield) of the title compound: 1H NMR (500 MHz, CDCl3); 0.8-0.9 (4H, m), 1.0-1.4 (5H, m), 1.5-1.8 (4H, m), 1.9-2.1 (1H, br s), 2.8-3.0 (2H, br s), 3.4-3.7 (2H, br d), 6.9 (1H, d), 7.1 (2H, d), 7.3-7.5 (2H, m), 8.1 (1H, d), 8.6 (1H, s); MS m/z 354 (M+1).
後処理
- filtrationFilter the reaction mixture
- customthe reaction at room temperature for 72 hours
- concentrationconcentrate the reaction mixture under reduced pressure
- additionAdd the reaction mixture to an SCX Column (2 g)
- washwash with methanol
- washelute with 1N NH3 MeOH
- concentrationConcentrate under reduced pressure and flash chromatograph
出典と根拠
- ORDレコード
- ord-2c6909afdcbc4859b12ef01c1baa8e05
- 出典データセット
- uspto-grants-2009_07
- 特許番号
- US07560463B2
反応ノート
読み込み中…