반응식
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C:9](O)=[CH:10][C:11](=O)[C:12]([F:15])([F:14])[F:13].[NH2:18][NH2:19]>C(O)(=O)C>[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C:9]1[NH:19][N:18]=[C:11]([C:12]([F:15])([F:14])[F:13])[CH:10]=1참가 물질
4
반응 조건
- 온도
- 95 °C
실험 절차
At 24° C., 15.0 g (0.06 mole) of the product of step A was dissolved in 50 mL glacial acetic acid and treated with 2 mL (0.064 mole) anhydrous hydrazine, added over a period of 5 minutes. The reaction was heated to 95° C. for 30 minutes. The reaction was cooled and poured into 300 mL ice water. The slurry was filtered and the cake washed with water and air dried to give 13.86 g (94%) of 5-(2,4-difluorophenyl)-3-(trifluoromethyl)-1H-pyrazole as a white solid, mp 157°-158° C.
후처리
- additionadded over a period of 5 minutes
- temperatureThe reaction was cooled
- filtrationThe slurry was filtered
- washthe cake washed with water and air
- customdried
출처 및 근거
- ORD 기록
- ord-3529431ae3f54028b402e174bf60e037
- 출처 데이터셋
- uspto-grants-1996_06
- 특허 번호
- US05530126
연결된 노트
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