Potassium Carbonate → HCID 58051757, compound
Reaction equation
[Br:1][C:2]1[C:6]([CH:7]=[O:8])=[C:5]([Br:9])[NH:4][N:3]=1.C(=O)([O-])[O-].[K+].[K+].[CH3:16][O:17][C:18]1[CH:25]=[CH:24][C:21]([CH2:22]Br)=[CH:20][CH:19]=1>CN(C)C=O>[Br:1][C:2]1[C:6]([CH:7]=[O:8])=[C:5]([Br:9])[N:4]([CH2:22][C:21]2[CH:24]=[CH:25][C:18]([O:17][CH3:16])=[CH:19][CH:20]=2)[N:3]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
3,5-Dibromo-1H-pyrazole-4-carbaldehyde (987.9 mg, 3.89 mmol) and potassium carbonate (1.613 g, 11.67 mmol) were dissolved in N,N-dimethylformamide (39 mL) at 25° C. under Ar. 4-methoxybenzyl bromide (617 μl, 4.28 mmol) was added dropwise. The reaction mixture was allowed to stir for 2 h 10 min. The reaction was stopped, quenched by addition of saturated aqueous ammonium chloride (30 mL), and the mixture extracted with ethyl acetate (3×30 mL). The combined organic phases were washed with saturated aqueous sodium chloride (1×20 mL), dried (sodium sulfate), filtered, and the solvent evaporated under reduced pressure. The crude product was purified by flash chromatography (RediSep SiO2, 120 g column) on a CombiFlash Rf purification system eluting with ethyl acetate-hexanes (0-55%). The title compound (L3342 g, 3.57 mmol, 92% yield) was recovered as a colorless, very viscous oil. LC-MS [M+1]=373.1.
Workup
- customquenched by addition of saturated aqueous ammonium chloride (30 mL)
- extractionthe mixture extracted with ethyl acetate (3×30 mL)
- washThe combined organic phases were washed with saturated aqueous sodium chloride (1×20 mL)
- dry with materialdried (sodium sulfate)
- filtrationfiltered
- customthe solvent evaporated under reduced pressure
- customThe crude product was purified by flash chromatography (RediSep SiO2, 120 g column) on a CombiFlash Rf purification system
- washeluting with ethyl acetate-hexanes (0-55%)
Sources & evidence
- ORD record
- ord-296842c992bb424fa1d9a98d385e9540
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08569512B2
Reaction notes
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