Potassium Phosphate, Tribasic → HCID 58042362, compound
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]1Participants
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
- customdegassed thoroughly
- customby bubbling nitrogen through the mixture
- temperaturethe reaction was heated to 95° C.
- temperaturethen cooled to room temperature
- filtrationThe mixture was filtered through arbocel
- washwashing with EtOAc
- concentrationthe filtrate concentrated in vacuo
- customThe residue was then purified by flash column chromatography
- 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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