반응식
[CH3:1][O:2][CH:3]1[C:8]([C:9]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[NH:11][CH:10]=2)=[CH:7][CH2:6][CH2:5][CH2:4]1>CCOC(C)=O.[Pd]>[CH3:1][O:2][CH:3]1[CH2:4][CH2:5][CH2:6][CH2:7][CH:8]1[C:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[NH:11][CH:10]=1참가 물질
4
실험 절차
Treat 3-(6-methoxy-cyclohex-1-enyl)-1H-indole (200 mg, 0.879 mmol) with 10% Pd/C (40 mg) in EtOAc under atmospheric hydrogenation conditions for 1.5 hours. Filter resulting solution over Celite to remove catalyst. Concentrate crude on rotovap and purify on silica gel chromatography to give 3-(2-Methoxy-cyclohexyl)-1H-indole (127 mg, 63% yield). Mass Spectrum (m/e): 230.03 (MH+), 228.14 (M−).
후처리
- filtrationFilter
- customresulting solution over Celite
- customto remove catalyst
- concentrationConcentrate crude on rotovap
- custompurify on silica gel chromatography
출처 및 근거
- ORD 기록
- ord-aaf33ef739f74ee9a12d9e05353dda82
- 출처 데이터셋
- uspto-grants-2007_10
- 특허 번호
- US07276516B2
연결된 노트
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