Hydrochloric Acid → 1-(3-Aminopropyl)-4,4-dicyclohexylpiperidine
반응식
[C:1]1([C:7]2([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[CH2:12][CH2:11][N:10]([CH2:13][CH2:14][C:15]#[N:16])[CH2:9][CH2:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[H][H].Cl.CCOCC.[OH-].[Na+]>CCO.O.[Pd]>[NH2:16][CH2:15][CH2:14][CH2:13][N:10]1[CH2:11][CH2:12][C:7]([CH:17]2[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]2)([CH:1]2[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]2)[CH2:8][CH2:9]1참가 물질
실험 절차
A solution of 3-(4,4-diphenylpiperidin-1-yl)propionitrile (1.01 g, 3.48 mmol, 1.00 equiv) in denatured EtOH (50 mL, 5% isopropanol) was stirred at 120-130° C. in the presence of 10% Pd on activated carbon (1.00 g, Aldrich) and hydrogen at 440 psi for 15 hours. The catalyst was filtered out by use of Celite and washed with CH2Cl2 (100 mL) and MeOH (150 mL). After removal of the solvents, the residue was dissolved in CH2Cl2 (10 mL) and treated with HCl in ether (1.0M., 8.7 mmol, 2.5 equiv). The solvents were removed again and the residue was recrystallized from hot EtOH-ether (1:2). The white solid obtained from filtration of this mixture was taken up in water (40 mL), which was basified to pH 10 by addition of 1N NaOH and extracted with CH2Cl2 (3×75 mL). The combined organic solutions were dried over MgSO4 and concentrated to afford 650 mg of colorless oil (61%), which was characterized spectroscopically.
후처리
- filtrationThe catalyst was filtered out by use of Celite
- washwashed with CH2Cl2 (100 mL) and MeOH (150 mL)
- customAfter removal of the solvents
- dissolutionthe residue was dissolved in CH2Cl2 (10 mL)
- customThe solvents were removed again
- customthe residue was recrystallized from hot EtOH-ether (1:2)
- customThe white solid obtained from filtration of this mixture
- extractionextracted with CH2Cl2 (3×75 mL)
- dry with materialThe combined organic solutions were dried over MgSO4
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-a43396ec388b4a6280f4c2082b43fbad
- 출처 데이터셋
- uspto-grants-2001_04
- 특허 번호
- US06211198B1
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