Hydrochloric Acid → 4-{N'-[2-(4-fluoro-phenyl)-acetyl]-N'-methyl-hydrazino}-piperidine-1-carboxylic acid tert-butyl ester
반응식
[CH3:1][N:2]([C:4](=[O:13])[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([F:12])=[CH:8][CH:7]=1)[NH2:3].[C:14]([O:18][C:19]([N:21]1[CH2:26][CH2:25][C:24](=O)[CH2:23][CH2:22]1)=[O:20])([CH3:17])([CH3:16])[CH3:15].[BH3-]C#N.[Na+].Cl.C(=O)(O)[O-].[Na+]>C(O)C>[C:14]([O:18][C:19]([N:21]1[CH2:26][CH2:25][CH:24]([NH:3][N:2]([C:4](=[O:13])[CH2:5][C:6]2[CH:11]=[CH:10][C:9]([F:12])=[CH:8][CH:7]=2)[CH3:1])[CH2:23][CH2:22]1)=[O:20])([CH3:17])([CH3:15])[CH3:16]참가 물질
반응물 5
생성물 1
시약·촉매·용매 1
실험 절차
To a stirred solution of (4-fluorophenyl)-acetic acid N-methyl-hydrazide, 8, (2 g, 11 mmol) in ethanol (20 mL) is added commercially available 4-oxo-piperidine-1-carboxylic acid tert-butyl ester (2.19 g, 11 mmol). The reaction mixture is refluxed for 30 minutes, then cooled to room temperature after which NaCNBH3 (1.04 g, 16,5 mmol) is added. The pH of the reaction mixture is adjusted to about 3 with concentrated HCl and the reaction mixture stirred for 3 hours at room temperature. The mixture is neutralized with saturated sodium bicarbonate and extracted three times with CH2Cl2. The combined organic layers are dried, filtered and concentrated in vacuo. Purification over silica (EtOAc) affords 3.7 g (93% yield) of the desired product. ESI/MS: 366.3 (M+H).
후처리
- temperatureThe reaction mixture is refluxed for 30 minutes
- additionis added
- extractionextracted three times with CH2Cl2
- customThe combined organic layers are dried
- filtrationfiltered
- concentrationconcentrated in vacuo
- customPurification over silica (EtOAc)
출처 및 근거
- ORD 기록
- ord-05754addf31a44d3be1c1fa90529b504
- 출처 데이터셋
- uspto-grants-2004_01
- 특허 번호
- US06677337B2
반응 노트
불러오는 중…