Water → 5-Amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-(1,2,4-oxadiazol-3-yl)-4-thiocyanato pyrazole
반응식
[S-:1][C:2]#[N:3].[K+].BrBr.[NH2:7][C:8]1[N:12]([C:13]2[C:18]([Cl:19])=[CH:17][C:16]([C:20]([F:23])([F:22])[F:21])=[CH:15][C:14]=2[Cl:24])[N:11]=[C:10]([C:25]2[N:29]=[CH:28][O:27][N:26]=2)[CH:9]=1.O>CO>[NH2:7][C:8]1[N:12]([C:13]2[C:18]([Cl:19])=[CH:17][C:16]([C:20]([F:23])([F:21])[F:22])=[CH:15][C:14]=2[Cl:24])[N:11]=[C:10]([C:25]2[N:29]=[CH:28][O:27][N:26]=2)[C:9]=1[S:1][C:2]#[N:3]참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- -78 °C
실험 절차
Potassium thiocyanate (1.45 g, 14.9 mmol) was dissolved in 20 ml of dry methanol, and then a methanol (5 ml) solution of bromine (0.28 ml, 5.44 mmol) was added dropwise with stirring at −78° C. over 8 minutes (inner temperature: not higher than −65° C.). After the completion of adding dropwise, the mixture was stirred at −78° C. for 10 minutes and a methanol (15 ml) solution of 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-(1,2,4-oxadiazol-3-yl)pyrazole (1.80 g, 4.94 mmol) was added dropwise over 15 minutes. The solution was stirred at −78° C. for 2 hours, warmed to room temperature and then stirred at the same temperature for 2 hours. The reaction mixture was poured into 100 ml of iced water. After stirring for 30 minutes, the deposited crystal was filtered. The resulting crystal was washed with water and then dried under reduced pressure to obtain 2.04 g (4.85 mmol) of the title compound as a colorless crystal. Yield 98.0%.
후처리
- customhigher than −65° C.
- additionAfter the completion of adding dropwise
- stirringthe mixture was stirred at −78° C. for 10 minutes
- stirringThe solution was stirred at −78° C. for 2 hours
- temperaturewarmed to room temperature
- stirringstirred at the same temperature for 2 hours
- stirringAfter stirring for 30 minutes
- filtrationthe deposited crystal was filtered
- washThe resulting crystal was washed with water
- customdried under reduced pressure
출처 및 근거
- ORD 기록
- ord-953c2617b17c4f66a6887d3fc80a9895
- 출처 데이터셋
- uspto-grants-2001_11
- 특허 번호
- US06316477B1
반응 노트
불러오는 중…