Potassium Phosphate, Tribasic → HCID 58042362, compound

HRID 512074Notes

Reaction equation

HRID 512074 reaction equation
[CH:1]1(B(O)O)[CH2:3][CH2:2]1.[O-]P([O-])([O-])=O.[K+].[K+].[K+].Br[C:16]1[C:21]([O:22][CH:23]([F:25])[F:24])=[CH:20][CH:19]=[CH:18][N:17]=1.C1(P(C2CCCCC2)C2CCCCC2)CCCCC1>C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH:1]1([C:16]2[C:21]([O:22][CH:23]([F:25])[F:24])=[CH:20][CH:19]=[CH:18][N:17]=2)[CH2:3][CH2:2]1

Participants

6

Conditions

Temperature
80 °C

Procedure

Cyclopropylboronic acid (383 mg, 4.5 mmol) and potassium phosphate tribasic (1.89 g, 8.9 mmol) were added to a solution of 2-bromo-3-difluoromethoxypyridine (Preparation 102, 570 mg, 2.5 mmol). The mixture was heated to 80° C. and degassed thoroughly by bubbling nitrogen through the mixture. After 30 minutes, the reaction was heated to 95° C. and tricyclohexylphosphine (84 mg, 0.30 mmol) was added followed by palladium acetate (32 mg, 0.14 mmol). The reaction was stirred at 95° C. for 18 hours then cooled to room temperature. The mixture was filtered through arbocel, washing with EtOAc and the filtrate concentrated in vacuo. The residue was then purified by flash column chromatography eluting with EtOAc:heptane 1:5 to afford the title compound as a colourless oil (273 mg, 58%).

Workup

  1. customdegassed thoroughly
  2. customby bubbling nitrogen through the mixture
  3. temperaturethe reaction was heated to 95° C.
  4. temperaturethen cooled to room temperature
  5. filtrationThe mixture was filtered through arbocel
  6. washwashing with EtOAc
  7. concentrationthe filtrate concentrated in vacuo
  8. customThe residue was then purified by flash column chromatography
  9. washeluting with EtOAc:heptane 1:5

Sources & evidence

ORD record
ord-d14d6e96ce4e482899074c5a1803dd8e
Source dataset
uspto-grants-2015_08
Patent number
US09102621B2

Reaction notes

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