반응식
Br[CH2:2][C:3]([C:5]1[C:6]([F:20])=[C:7]2[O:11][C:10]([CH:12]3[CH2:14][CH2:13]3)=[N:9][C:8]2=[C:15]([C:18]#[N:19])[C:16]=1[CH3:17])=O.C(=O)([O-])[O-].[Cs+].[Cs+].[C:27]([NH2:30])(=[S:29])[CH3:28]>C1(C)C=CC=CC=1>[CH:12]1([C:10]2[O:11][C:7]3[C:8](=[C:15]([C:18]#[N:19])[C:16]([CH3:17])=[C:5]([C:3]4[N:30]=[C:27]([CH3:28])[S:29][CH:2]=4)[C:6]=3[F:20])[N:9]=2)[CH2:14][CH2:13]1참가 물질
반응 조건
- 온도
- 100 °C
실험 절차
6-(2-Bromoacetyl)-2-cyclopropyl-7-fluoro-5-methyl-1,3-benzoxazole-4-carbonitrile (I-79) (39.98 g, 28.6 mmol) was dissolved in toluene (270 ml), then cesium carbonate (13.02 g, 39.90 mmol) and thioacetamide (2.58 g, 34.28 mmol) were added, followed by stirring at 100° C. for 6 hours under nitrogen atmosphere. The reaction liquid was cooled, the insoluble matter was separated by filtration through Celite, ethyl acetate was added to the filtrate, followed by washing with water and saturated brine. The obtained organic layer was dried over anhydrous sodium sulfate, the solvent was evaporated away under reduced pressure. The resulting residue was recrystallized and purified with n-hexane/ethyl acetate to obtain the entitled compound (3.96 g, 44%) as a white solid.
후처리
- customThe reaction liquid
- temperaturewas cooled
- customthe insoluble matter was separated by filtration through Celite, ethyl acetate
- additionwas added to the filtrate
- washby washing with water and saturated brine
- dry with materialThe obtained organic layer was dried over anhydrous sodium sulfate
- customthe solvent was evaporated away under reduced pressure
- customThe resulting residue was recrystallized
- custompurified with n-hexane/ethyl acetate
출처 및 근거
- ORD 기록
- ord-f02d5e1c41b3406881161b6fbf955e13
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07737166B2
연결된 노트
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