Boron trifluoride → 1-[5-(Chloro)-2-(4-methoxyphenyl) pyrazolo[1,5-alpha]pyridin-3-yl]ethanone

HRID 724001노트

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HRID 724001 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][N:5]2[N:8]=[C:9]([C:11]3[CH:16]=[CH:15][C:14]([O:17][CH3:18])=[CH:13][CH:12]=3)[CH:10]=[C:4]2[CH:3]=1.[C:19](OC(=O)C)(=[O:21])[CH3:20].B(F)(F)F>C1(C)C=CC=CC=1>[Cl:1][C:2]1[CH:7]=[CH:6][N:5]2[N:8]=[C:9]([C:11]3[CH:12]=[CH:13][C:14]([O:17][CH3:18])=[CH:15][CH:16]=3)[C:10]([C:19](=[O:21])[CH3:20])=[C:4]2[CH:3]=1

참가 물질

5

실험 절차

To a solution of 5-chloro-2-(4-methoxyphenyl)pyrazolo[1,5-α]pyridine (3.0 g, 11.6 mmol) in toluene (100 mL) at room temperature was added acetic anhydride (1.6 mL, 17.4 mmol). Boron trifluoride diethyletherate (1.8 mL, 13.9 mmol) was then added dropwise and the resulting solution was heated at reflux for 4 hours. The reaction mixture was cooled to room temperature and quenched by the dropwise addition of saturated aqueous sodium bicarbonate. The reaction was extracted with ethyl acetate, and the ethyl acetate phase washed with brine, dried (magnesium sulfate), filtered and concentrated. The residue was purified by recrystallization from ethyl acetate-hexanes to give 1-[5-(chloro)-2-(4-methoxyphenyl)pyrazolo[1,5-α]pyridin-3-yl]ethanone (2.31 g, 66%). 1H NMR (CDCl3): δ 8.44 (d, 1H), 8.40 (d, 1H), 7.49 (d, 2H), 7.02 (d, 2H), 6.97 (dd, 1H), 3.85 (s, 3H), 2.15 (s, 3H); MS m/z 301 (M+1).

후처리

  1. temperaturethe resulting solution was heated
  2. temperatureat reflux for 4 hours
  3. customquenched by the dropwise addition of saturated aqueous sodium bicarbonate
  4. extractionThe reaction was extracted with ethyl acetate
  5. washthe ethyl acetate phase washed with brine
  6. dry with materialdried (magnesium sulfate)
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customThe residue was purified by recrystallization from ethyl acetate-hexanes

출처 및 근거

ORD 기록
ord-1e815a14184b485f8751bb5f3282dd61
출처 데이터셋
uspto-grants-2006_11
특허 번호
US07141569B2

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