반응식
O.C1(C)C=CC(S(O)(=O)=O)=CC=1.[Br:13][C:14]1[C:15](O)=[C:16]([NH:31][C:32](=[O:37])[C:33]([CH3:36])([CH3:35])[CH3:34])[C:17]([C:29]#[N:30])=[C:18]([CH3:28])[C:19]=1[CH:20]=[CH:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1.O.C(=O)(O)[O-].[Na+]>C1(C)C=CC=CC=1>[Br:13][C:14]1[C:19]([CH:20]=[CH:21][C:22]2[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=2)=[C:18]([CH3:28])[C:17]([C:29]#[N:30])=[C:16]2[C:15]=1[O:37][C:32]([C:33]([CH3:36])([CH3:35])[CH3:34])=[N:31]2참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
Toluene (3 ml), p-toluenesulfonic acid monohydrate (1.4 mg, 7.5 μmol) were added to N-(3-bromo-6-cyano-2-hydroxy-5-methyl-4-styrylphenyl)-2,2-dimethylpropionamide (I-14) (31 mg, 75 μmol), followed by refluxing with a Dean-Stark condenser for 2.5 hours. After cooling, saturated sodium bicarbonate water (30 ml) was added to the reaction liquid, the product was extracted with ethyl acetate (30 ml×2). The organic layer was washed with saturated brine (30 ml), dried over anhydrous magnesium sulfate, concentrated under reduced pressure, the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=8:1) to obtain the entitled compound (25 mg, 84%) as a colorless solid.
후처리
- temperatureby refluxing with a Dean-Stark condenser for 2.5 hours
- temperatureAfter cooling
- extractionthe product was extracted with ethyl acetate (30 ml×2)
- washThe organic layer was washed with saturated brine (30 ml)
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated under reduced pressure
- customthe residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=8:1)
출처 및 근거
- ORD 기록
- ord-ff74efec60a34a189d6388ef3f692111
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07737166B2
연결된 노트
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