Potassium Carbonate → HCID 68699101, compound
Reaction equation
[OH:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][N:3]=1.Br[C:10]1[CH:14]=[CH:13][S:12][CH:11]=1.C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O.[OH-].[NH4+].[Cu]I>[CH3:8][C:6]1[CH:5]=[CH:4][N:3]([C:10]2[CH:14]=[CH:13][S:12][CH:11]=2)[C:2](=[O:1])[CH:7]=1Participants
7
Reactant 3
Product 1
Reagents, catalysts & solvents 3
Conditions
- Temperature
- 150 °C
Procedure
A mixture of 2-hydroxy-4-methylpyridine (1.5 g, 14 mmol), 3-bromothiophene (4.5 g, 28 mmol), copper (I) iodide (0.27 g, 1.4 mmol), and potassium carbonate (1.9 g, 14 mmol) in N,N-dimethylformamide (30 mL) is heated in a 150° C. oil bath for 6 hours. After cooling to room temperature, the reaction mixture is diluted with 20% aqueous ammonium hydroxide solution and extracted 3× with diethyl ether. The combined extracts were washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give a crude oil, which is purified by flash chromatography (ethyl acetate/hexanes) to give 4-methyl-1-(3-thienyl)pyridin-2(1H)-one (0.79 g, 29%).
Workup
- temperatureAfter cooling to room temperature
- extractionextracted 3× with diethyl ether
- washThe combined extracts were washed with saturated aqueous sodium chloride solution
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated under reduced pressure
- customto give a crude oil, which
- customis purified by flash chromatography (ethyl acetate/hexanes)
Sources & evidence
- ORD record
- ord-53bc25b0e22349fdb1ad7577d70565c8
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07713994B2
Reaction notes
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