1,2-Diaminocyclohexane, (+)- → ethyl 4-[4-[[(1S,2S)-2-aminocyclohexyl]amino]-1-piperidyl]-4-methyl-piperidine-1-carboxylate
반응식
[CH3:1][C:2]1([N:13]2[CH2:18][CH2:17][C:16](=O)[CH2:15][CH2:14]2)[CH2:7][CH2:6][N:5]([C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH2:4][CH2:3]1.[C@H:20]1([NH2:27])[CH2:25][CH2:24][CH2:23][CH2:22][C@@H:21]1[NH2:26].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C([O-])(O)=O.[Na+]>ClCCl>[NH2:26][C@H:21]1[CH2:22][CH2:23][CH2:24][CH2:25][C@@H:20]1[NH:27][CH:16]1[CH2:17][CH2:18][N:13]([C:2]2([CH3:1])[CH2:7][CH2:6][N:5]([C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH2:4][CH2:3]2)[CH2:14][CH2:15]1참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
To a solution ethyl 4-methyl-4-(4-oxo-1-piperidyl)piperidine-1-carboxylate (336 mg, 1.25 mmol) and (1S,2S)-cyclohexane-1,2-diamine (286 mg, 0.5 mmol) in dichloromethane (10 mL) was added sodium triacetoxyborohydride (398 mg, 1.88 mmol) and stirred at room temperature for 12 h. Saturated NaHCO3 (5 mL) was added, the phases were separated and the aqueous phase was extracted with dichloromethane (2×10 mL). The combined organic phases were washed with brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified by passing through a short silica gel pad (5-10% MeOH in dichloromethane) to afford the title compound (87 mg, 19%). MS (M+1): 367.31.
후처리
- customthe phases were separated
- extractionthe aqueous phase was extracted with dichloromethane (2×10 mL)
- washThe combined organic phases were washed with brine
- dry with materialdried over Na2SO4
- concentrationconcentrated in vacuo
- customThe residue was purified
출처 및 근거
- ORD 기록
- ord-1b97ca16fe42434790770a17b98194ed
- 출처 데이터셋
- uspto-grants-2012_02
- 특허 번호
- US08119661B2
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