반응식
[C:1]1([C:7]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[N:8]2[CH2:13][CH2:12][C:11](=[O:14])[CH2:10][CH2:9]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.N1CCCC1.[CH:32](=O)[C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1>C1C=CC=CC=1.C(OCC)(=O)C>[CH:32](=[C:10]1/[CH2:9][N:8]([C:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)([C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)[C:21]2[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=2)[CH2:13][CH2:12][C:11]/1=[O:14])/[C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1참가 물질
실험 절차
To a solution of 1-(triphenylmethyl)piperidin-4-one (4.22 g) in benzene (50 ml) was added pyrrolidine (1.02 ml) at room temperature, and the resulting mixture was refluxed for 3 hours. After cooling to room temperature, benzaldehyde (1.26 ml) was added to the reaction mixture, and the resulting mixture was furthermore refluxed for 2 hours. After refluxing, the reaction mixture was diluted with ethyl acetate, washed with saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was removed in vacuo, and the residue was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (1:3) as the eluent to afford the title compound (3.92 g, yield: 74%) as a yellow oil.
후처리
- temperaturethe resulting mixture was refluxed for 3 hours
- temperaturethe resulting mixture was furthermore refluxed for 2 hours
- temperatureAfter refluxing
- washwashed with saturated aqueous sodium chloride solution
- dry with materialdried over anhydrous sodium sulfate
- customThe solvent was removed in vacuo
- customthe residue was purified by chromatography on a silica gel column
출처 및 근거
- ORD 기록
- ord-2834e8323229450fa7d7f6c49b06546f
- 출처 데이터셋
- uspto-grants-2010_11
- 특허 번호
- US07829580B2
연결된 노트
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