Potassium Carbonate → 3-(4-Methyl-2-nitro-phenyl)-pyridine

HRID 227235

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HRID 227235 반응식
Br[C:2]1[CH:7]=[CH:6][C:5](O)=[C:4]([N+:9]([O-:11])=[O:10])[CH:3]=1.[N:12]1[CH:17]=[CH:16][CH:15]=[C:14](B(O)O)[CH:13]=1.[C:21](=O)([O-])[O-].[K+].[K+]>O1CCOCC1.O.CCOC(C)=O.C([O-])([O-])=O.[Na+].[Na+].[Pd].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[CH3:21][C:2]1[CH:7]=[CH:6][C:5]([C:14]2[CH:13]=[N:12][CH:17]=[CH:16][CH:15]=2)=[C:4]([N+:9]([O-:11])=[O:10])[CH:3]=1

참가 물질

9

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온도
70 °C

실험 절차

4-Bromo-2-nitro-phenol (648 mg, 3.0 mmol) and 3-pyridyl boronic acid (387 mg, 3.15 mmol) were diluted with 5 mL of dioxane and placed under N2. Potassium carbonate was diluted in 1 mL of H2O and added to the reaction mixture. Tetrakis(triphenylphosphine) palladium (173 mg, 0.15 mmol) was added, then the reaction was heated to 70° C. and stirred overnight. The reaction was allowed to cool to room temperature, then diluted with 30 mL of EtOAc and 30 mL of 10% Na2CO3. The organic layer was washed with brine, dried over MgSO4, filtered, and concentrated under reduced pressure. The material was purified with a Biotage 40M cartridge eluting with hexanes/EtOAc, 1/1 to yield an off white solid.

후처리

  1. additionadded to the reaction mixture
  2. temperatureto cool to room temperature
  3. washThe organic layer was washed with brine
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customThe material was purified with a Biotage 40M cartridge
  8. washeluting with hexanes/EtOAc, 1/1
  9. customto yield an off white solid

출처 및 근거

ORD 기록
ord-1cd7e63882694d8b92fa652bbf8ab09d
출처 데이터셋
uspto-grants-2009_07
특허 번호
US07560462B2

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