Potassium Carbonate → 3-Bromo-5-(4-(pyrrolidine-1-sulfonyl)phenoxy)pyridine

HRID 2212138

반응식

HRID 2212138 반응식
[Br:1][C:2]1[CH:3]=[C:4]([OH:8])[CH:5]=[N:6][CH:7]=1.F[C:10]1[CH:15]=[CH:14][C:13]([S:16]([N:19]2[CH2:23][CH2:22][CH2:21][CH2:20]2)(=[O:18])=[O:17])=[CH:12][CH:11]=1.C(=O)([O-])[O-].[K+].[K+]>CC(N(C)C)=O>[Br:1][C:2]1[CH:7]=[N:6][CH:5]=[C:4]([O:8][C:10]2[CH:15]=[CH:14][C:13]([S:16]([N:19]3[CH2:20][CH2:21][CH2:22][CH2:23]3)(=[O:18])=[O:17])=[CH:12][CH:11]=2)[CH:3]=1

참가 물질

5

반응 조건

온도
120 °C

실험 절차

A mixture of 5-bromo-3-pyridinol (2.61 g, 15 mmol), dimethylacetamide (50 mL), 1-((4-fluorophenyl)sulfonyl)pyrrolidine (5.8 g, 25 mmol) and potassium carbonate (4.1 g, 30 mmol) was heated at 120° C. for 18 h, then cooled to room temperature and concentrated by rotary evaporation. The residue was dissolved in ethyl acetate (200 mL) and the organic phase washed with water (3×100 mL) and brine (100 mL), then dried (MgSO4), filtered and concentrated by rotary evaporation. The crude product was purified by column chromatography, eluting with ethyl acetate/cyclohexane (20/80, v/v). Selected fractions containing the product were concentrated via rotary evaporation to give 3.4 g (59%) of a red solid (m.p. 148° C.)

후처리

  1. temperaturecooled to room temperature
  2. concentrationconcentrated by rotary evaporation
  3. dissolutionThe residue was dissolved in ethyl acetate (200 mL)
  4. washthe organic phase washed with water (3×100 mL) and brine (100 mL)
  5. dry with materialdried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated by rotary evaporation
  8. customThe crude product was purified by column chromatography
  9. washeluting with ethyl acetate/cyclohexane (20/80
  10. additionSelected fractions containing the product
  11. concentrationwere concentrated via rotary evaporation

출처 및 근거

ORD 기록
ord-3c5af9c391014883b283a8713acbd156
출처 데이터셋
uspto-grants-2006_09
특허 번호
US07101896B2

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