Trifluoroacetic acid → 3-(1H-pyrazol-4-yl)benzonitrile trifluoroacetate
반응식
C[Si](C)(C)CCOC[N:7]1[CH:11]=[C:10]([C:12]2[CH:13]=[C:14]([CH:17]=[CH:18][CH:19]=2)[C:15]#[N:16])[CH:9]=[N:8]1.[C:22]([OH:28])([C:24]([F:27])([F:26])[F:25])=[O:23]>>[F:25][C:24]([F:27])([F:26])[C:22]([OH:28])=[O:23].[NH:7]1[CH:11]=[C:10]([C:12]2[CH:13]=[C:14]([CH:17]=[CH:18][CH:19]=2)[C:15]#[N:16])[CH:9]=[N:8]1참가 물질
3
반응 조건
- 온도
- 120 °C
실험 절차
A solution of 3-(1-[2-(trimethylsilyl)ethoxy]methyl-1H-pyrazol-4-yl)benzonitrile (110.0 mg, 0.0003673 mol) was taken up in TFA (3.0 mL, 0.039 mol) and the mixture was heated in microwave at 120° C. for 3 min. The reaction mixture was allowed to cool to rt, and then concentrated to give a crude residue. The product was purified by HPLC on a C-18 column eluting with a water/ACN gradient containing 0.2% TFA to give 3-(1H-pyrazol-4-yl)benzonitrile trifluoroacetate as an amorphous white solid, LC/MS (M+H)+: 170.
후처리
- temperatureto cool to rt
- concentrationconcentrated
- customto give a crude residue
- customThe product was purified by HPLC on a C-18 column
- washeluting with a water/ACN gradient
- additioncontaining 0.2% TFA
출처 및 근거
- ORD 기록
- ord-9d289ccac2554d1885e760b9a4d231f0
- 출처 데이터셋
- uspto-grants-2015_01
- 특허 번호
- US08933086B2
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