Pyrazole → 2-(1H-pyrazol-1-yl)-9-(tetrahydro-2H-pyran-2-yl)-9H-carbazole
반응식
Br[C:2]1[CH:14]=[CH:13][C:12]2[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[N:5]([CH:15]3[CH2:20][CH2:19][CH2:18][CH2:17][O:16]3)[C:4]=2[CH:3]=1.[NH:21]1[CH:25]=[CH:24][CH:23]=[N:22]1.C(=O)([O-])[O-].[K+].[K+].N1CCC[C@H]1C(O)=O>[Cu]I>[N:21]1([C:2]2[CH:14]=[CH:13][C:12]3[C:11]4[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=4)[N:5]([CH:15]4[CH2:20][CH2:19][CH2:18][CH2:17][O:16]4)[C:4]=3[CH:3]=2)[CH:25]=[CH:24][CH:23]=[N:22]1참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 90 °C
실험 절차
Under a nitrogen atmosphere, 10 mmol of 2-bromo-9-(tetrahydro-2H-pyran-2-yl)-9H-carbazole, 15 mmol of pyrazole, 1 mmol of copper(I)iodide, 25 mmol of potassium carbonate, and 2 mmol of L-proline were combined in 25 mL of stirring degassed dimethyl sulfoxide. The mixture was heated to 90° C. for 3 days before being cooled and separated between dichloromethane and water. The water layer was washed twice with dichloromethane and the organics were combined and washed once with brine. The organic fraction was dried with magnesium sulfate and concentrated under reduced pressure and subjected to column chromatography of silica with dichloromethane as the eluent. After concentrating under reduced pressure, 2-(1H-pyrazol-1-yl)-9-(tetrahydro-2H-pyran-2-yl)-9H-carbazole was isolated in a 40% yield.
후처리
- customdegassed dimethyl sulfoxide
- temperaturebefore being cooled
- customseparated between dichloromethane and water
- washThe water layer was washed twice with dichloromethane
- washwashed once with brine
- dry with materialThe organic fraction was dried with magnesium sulfate
- concentrationconcentrated under reduced pressure
- concentrationAfter concentrating under reduced pressure
출처 및 근거
- ORD 기록
- ord-a8647f4ff43448d8a79412c80779f585
- 출처 데이터셋
- uspto-grants-2016_01
- 특허 번호
- US09238668B2
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