반응식
[NH2:1][C:2]1[CH:6]=[CH:5]NN=1.CO[C:9](=[O:20])[C:10]1[CH:15]=[CH:14][C:13]([C:16]([F:19])([F:18])[F:17])=[CH:12][CH:11]=1.[H-].[Na+].C(#N)CC>>[CH3:5][CH:6]([C:9](=[O:20])[C:10]1[CH:11]=[CH:12][C:13]([C:16]([F:17])([F:18])[F:19])=[CH:14][CH:15]=1)[C:2]#[N:1]참가 물질
5
실험 절차
The product was prepared according to the general procedure for aminopyrazole synthesis (route A1) from 4-trifluoromethyl-benzoic acid methyl ester (3.0 g, 14.7 mmol, 1.0 eq), NaH (1.2 g, 29.4 mmol, 2.0 eq) and propionitrile (4.9 mL, 69.4 mmol, 4.7 eq). The crude product was extracted with DCM and used in the following step without further purification (3.2 g, yield: 96%).
후처리
- customThe product was prepared
- extractionThe crude product was extracted with DCM
- customused in the following step without further purification (3.2 g, yield: 96%)
출처 및 근거
- ORD 기록
- ord-bd720de13d4141079f412edd57df2be6
- 출처 데이터셋
- uspto-grants-2012_04
- 특허 번호
- US08163729B2
연결된 노트
불러오는 중…