Acetonitrile → HCID 57930994, compound
Reaction equation
[CH3:1][N:2]1[CH:6]=[CH:5][C:4](B2OC(C)(C)C(C)(C)O2)=[N:3]1.P([O-])([O-])([O-])=O.[K+].[K+].[K+].C(#N)C.Br[C:28]1[CH:37]=[CH:36][C:31]([C:32]([O:34][CH3:35])=[O:33])=[CH:30][C:29]=1[O:38][CH2:39][CH3:40]>O>[CH2:39]([O:38][C:29]1[CH:30]=[C:31]([CH:36]=[CH:37][C:28]=1[C:5]1[CH:4]=[N:3][N:2]([CH3:1])[CH:6]=1)[C:32]([O:34][CH3:35])=[O:33])[CH3:40]Participants
Conditions
- Temperature
- 100 °C
Procedure
1-Methyl-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (183 mg, 0.88 mmol), potassium phosphate (374 mg, 1.76 mmol) and dichloro(1,1-bis(diphenylphosphino)-ferrocene)palladium(II) dichloromethane adduct (9.6 mg, 0.012 mmol) were added to an acetonitrile solution (3 mL) of methyl 4-bromo-3-ethoxybenzoate (152 mg, 0.59 mmol), and stirred overnight at 100° C. The reaction liquid was cooled to room temperature, and water was added to it. This was extracted with ethyl acetate, washed with saturated saline water, and dried with magnesium sulfate. The solution was filtered, and concentrated under reduced pressure, and the resulting residue was purified through silica gel column chromatography (hexane/ethyl acetate=50/50) to obtain the title compound as a white solid.
Workup
- customThe reaction liquid
- temperaturewas cooled to room temperature
- extractionThis was extracted with ethyl acetate
- washwashed with saturated saline water
- dry with materialdried with magnesium sulfate
- filtrationThe solution was filtered
- concentrationconcentrated under reduced pressure
- customthe resulting residue was purified through silica gel column chromatography (hexane/ethyl acetate=50/50)
Sources & evidence
- ORD record
- ord-365589fdf9c54fb99f0feb703fbad90c
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08138197B2
Reaction notes
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