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Ethyl bromodifluoroacetate → Ethyl 2-(4-(4-(2-ethoxy-2-oxoethyl)phenyl)pyridin-2-yl)-2,2-difluoroacetate

HRID 1036273
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HRID 1036273 반응식
Br[C:2]1[CH:7]=[C:6]([C:8]2[CH:13]=[CH:12][C:11]([CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16])=[CH:10][CH:9]=2)[CH:5]=[CH:4][N:3]=1.Br[C:21]([F:28])([F:27])[C:22]([O:24][CH2:25][CH3:26])=[O:23]>CN(C=O)C>[CH2:18]([O:17][C:15](=[O:16])[CH2:14][C:11]1[CH:12]=[CH:13][C:8]([C:6]2[CH:5]=[CH:4][N:3]=[C:2]([C:21]([F:28])([F:27])[C:22]([O:24][CH2:25][CH3:26])=[O:23])[CH:7]=2)=[CH:9][CH:10]=1)[CH3:19]
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참가 물질

4

반응물 2

HCID 69585Ethyl bromodifluoroacetateHCID 58447951Ethyl 2-(4-(2-bromopyridin-4-yl)phenyl)acetate

생성물 1

HCID 58447939Ethyl 2-(4-(4-(2-ethoxy-2-oxoethyl)phenyl)pyridin-2-yl)-2,2-difluoroacetate

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
80 °C

실험 절차

To a sealed tube were added ethyl 2-(4-(2-bromopyridin-4-yl)phenyl)acetate 203-3 (440 mg, 1.37 mmol), ethyl 2-bromo-2,2-difluoroacetate (1.7 mL, 13.7 mmol), Cu (1.3 g, 20.6 mmol) and DMF (5 mL). The reaction mixture was bubbled with nitrogen for 1 minute and stirred at 80° C. for 1 hour. After cooling to room temperature, the mixture was filtered through a layer of Celite and concentrated. The residue was purified by silica gel flash chromatography and eluted with 20% ethyl acetate in hexane to give ethyl 2-(4-(4-(2-ethoxy-2-oxoethyl)phenyl)pyridin-2-yl)-2,2-difluoroacetate 203-4. MS m/z 364.2 (M+1).

후처리

  1. customThe reaction mixture was bubbled with nitrogen for 1 minute
  2. temperatureAfter cooling to room temperature
  3. filtrationthe mixture was filtered through a layer of Celite
  4. concentrationconcentrated
  5. customThe residue was purified by silica gel flash chromatography
  6. washeluted with 20% ethyl acetate in hexane

출처 및 근거

ORD 기록
ord-64744c078f5b403bbdf91e422ffc2231
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08546396B2

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