Sulfuric Acid → 6-(trifluoromethyl)-1H-indazol-5-amine
반응식
[N+]([O-])([O-])=O.[Na+].[F:6][C:7]([F:18])([F:17])[C:8]1[CH:16]=[C:15]2[C:11]([CH:12]=[N:13][NH:14]2)=[CH:10][CH:9]=1.S(=O)(=O)(O)O.O.[NH3:25]>>[NH2:25][C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][C:8]=1[C:7]([F:6])([F:17])[F:18])[NH:14][N:13]=[CH:12]2참가 물질
실험 절차
Under ice-cooling, 1.01 g (12.0 mmol) of sodium nitrate was added to a mixture of 1.54 g (8.29 mmol) of 6-trifluoromethylindazole and 5 ml of concentrated sulfuric acid, and the mixture was stirred for 1 hour. The reaction mixture was poured onto ice and after ammonia water was added dropwise to the mixture under ice-cooling until pH reached 10 or higher, the precipitated solid was collected by filtration and then washed with water, followed by drying. The resulting crude product was dissolved in 50 ml of methanol, activated carbon was added to the mixture, and the mixture was filtered. 0.20 g of 5% Palladium-on-carbon was added to the filtrate, and the mixture was stirred under a hydrogen atmosphere at room temperature for 14 hours. The mixture was filtered through Celite and the filtrate was concentrated under reduced pressure to give 1.57 g (yield: 94%, two steps) of 5-amino-6-trifluoromethylindazole.
후처리
- temperatureUnder ice-cooling
- additionThe reaction mixture was poured onto ice
- temperaturecooling until pH
- filtrationhigher, the precipitated solid was collected by filtration
- washwashed with water
- customby drying
- dissolutionThe resulting crude product was dissolved in 50 ml of methanol
- additionactivated carbon was added to the mixture
- filtrationthe mixture was filtered
- addition0.20 g of 5% Palladium-on-carbon was added to the filtrate
- stirringthe mixture was stirred under a hydrogen atmosphere at room temperature for 14 hours
- filtrationThe mixture was filtered through Celite
- concentrationthe filtrate was concentrated under reduced pressure
출처 및 근거
- ORD 기록
- ord-fe4bce7044bb4b86bfea569bdf17a5e4
- 출처 데이터셋
- uspto-grants-2011_02
- 특허 번호
- US07879887B2
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