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

HRID 1621943

反応式

HRID 1621943 の反応式
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

参加物

6

反応条件

温度
0 °C

実験手順

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 5N 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.

後処理

  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 5N 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

出典と根拠

ORDレコード
ord-7bd1722ddee34de896fb4a9ea106adee
出典データセット
uspto-grants-2014_07
特許番号
US08772480B2

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