반응식
[F:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[CH:4][C:3]=1[C@H:9]1[CH2:15][N:14]([CH2:16][C:17]([F:20])([F:19])[F:18])[C:13](=[O:21])[C@H:12]([NH:22]C(=O)OC(C)(C)C)[CH2:11][CH2:10]1.C(C(O)=O)(F)(F)F>C(Cl)Cl>[NH2:22][C@@H:12]1[CH2:11][CH2:10][C@@H:9]([C:3]2[CH:4]=[CH:5][CH:6]=[C:7]([F:8])[C:2]=2[F:1])[CH2:15][N:14]([CH2:16][C:17]([F:20])([F:18])[F:19])[C:13]1=[O:21]참가 물질
4
실험 절차
To a solution of tert-butyl (3R,6S)-6-(2,3-difluorophenyl)-2-oxo-1-(2,2,2-trifluoroethyl)azepan-3-ylcarbamate from Step F (135 mg, 0.320 mmol) in CH2Cl2 (5 mL) was added CF3CO2H (2.5 mL). After 30 min, the solution was concentrated in vacuo and azeotroped with toluene (2×). Saturated aqueous NaHCO3 was added and the mixture was extracted with CH2Cl2 (3×). The combined organic extracts were washed with brine, dried over MgSO4, filtered and concentrated in vacuo to give the title compound. MS: m/z=323 (M+1).
후처리
- concentrationthe solution was concentrated in vacuo
- customazeotroped with toluene (2×)
- additionSaturated aqueous NaHCO3 was added
- extractionthe mixture was extracted with CH2Cl2 (3×)
- washThe combined organic extracts were washed with brine
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo
출처 및 근거
- ORD 기록
- ord-0c228504b75043de85c9f06cdf76478a
- 출처 데이터셋
- uspto-grants-2008_06
- 특허 번호
- US07390798B2
연결된 노트
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