Diisopropylamine → 2-Fluoro-5-methoxypyridine-3-boronic acid

HRID 1812352

반응식

HRID 1812352 반응식
C(NC(C)C)(C)C.[Li]CCCC.[F:13][C:14]1[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][N:15]=1.[B:22](OC(C)C)([O:27]C(C)C)[O:23]C(C)C>C1COCC1>[F:13][C:14]1[C:19]([B:22]([OH:27])[OH:23])=[CH:18][C:17]([O:20][CH3:21])=[CH:16][N:15]=1

참가 물질

6

반응 조건

온도
0 °C

실험 절차

To a 100 mL round-bottomed flask, diisopropylamine (Aldrich, 1.40 mL, 9.99 mmol) was dissolved into THF (6 mL). nBuLi (Aldrich, 2.5 M in hexanes, 3.60 mL, 8.99 mmol) was added slowly at 0° C. The mixture was stirred at 0° C. for 30 min then cooled to −78° C. 2-fluoro-5-methoxypyridine (0.520 g, 4.09 mmol) in 4 mL of THF was added slowly, and the mixture was stirred at that temperature for 40 min. Triisopropyl borate (Aldrich, 2.07 mL, 8.99 mmol) in a total of 4 mL of THF was added slowly and the mixture was stirred at −78° C. for 5 min. The cold bath was removed and the reaction mixture was stirred at room temperature for 1 h. 1 N NaOH (20 mL) was added to the mixture to quench the reaction. The layers were separated and the aqueous phase was treated with 5 N HCl to adjust the pH to around 5. The aqueous phase was extracted with EtOAc (2×20 mL). The combined organic phases were dried over sodium sulfate, filtered and concentrated in vacuo to afford 0.593 g of tan color solid. This material was used in the next step without further purification.

후처리

  1. temperaturethen cooled to −78° C
  2. stirringthe mixture was stirred at that temperature for 40 min
  3. stirringthe mixture was stirred at −78° C. for 5 min
  4. customThe cold bath was removed
  5. stirringthe reaction mixture was stirred at room temperature for 1 h
  6. addition1 N NaOH (20 mL) was added to the mixture
  7. customto quench
  8. customthe reaction
  9. customThe layers were separated
  10. additionthe aqueous phase was treated with 5 N HCl
  11. extractionThe aqueous phase was extracted with EtOAc (2×20 mL)
  12. dry with materialThe combined organic phases were dried over sodium sulfate
  13. filtrationfiltered
  14. concentrationconcentrated in vacuo
  15. customto afford 0.593 g of tan color solid
  16. customThis material was used in the next step without further purification

출처 및 근거

ORD 기록
ord-1c78278a360b4081835657ec07a8e3d2
출처 데이터셋
uspto-grants-2013_01
특허 번호
US08362241B2

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