Potassium Carbonate → HCID 18472402, compound
Reaction equation
[OH:1][CH:2]([C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][N:28]=1)[C:3]1[CH:8]=[CH:7][C:6]([NH:9][C:10](=[O:26])/[CH:11]=[CH:12]/[C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([C:19]3[CH:24]=[CH:23][C:22]([CH3:25])=[CH:21][CH:20]=3)[CH:14]=2)=[CH:5][CH:4]=1.C1C=C(Cl)C=C(C(OO)=[O:41])C=1.S([O-])([O-])(=O)=S.[Na+].[Na+].C(=O)([O-])[O-].[K+].[K+]>C1COCC1>[OH:1][CH:2]([C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][N+:28]=1[O-:41])[C:3]1[CH:8]=[CH:7][C:6]([NH:9][C:10](=[O:26])/[CH:11]=[CH:12]/[C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([C:19]3[CH:24]=[CH:23][C:22]([CH3:25])=[CH:21][CH:20]=3)[CH:14]=2)=[CH:5][CH:4]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
In THF (10 ml) was dissolved (E)-N-[4-[hydroxy(2-pyridyl)methyl]phenyl]-3-(4-methylphenyl)cinnamamide (200 mg), and to the mixture was added 70% mCPBA (152 mg). The mixture was stirred at room temperature for 6 hours, and to the solution were added saturated sodium thiosulfate solution (10 ml) and saturated potassium carbonate (10 ml). The mixture was stirred at room temperature for 30 minutes and extracted with ethyl acetate. The organic layer was washed with saturated sodium chloride solution, dried with anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was recrystallized from ethyl acetate-methanol to give (E)-N-[4-[hydroxy(1-oxido-2-pyridyl)methyl]phenyl]-3-(4-methylphenyl)cinnamamide (Compound 80) (123 mg) as colorless crystals.
Workup
- stirringThe mixture was stirred at room temperature for 30 minutes
- extractionextracted with ethyl acetate
- washThe organic layer was washed with saturated sodium chloride solution
- dry with materialdried with anhydrous sodium sulfate
- concentrationconcentrated under reduced pressure
- customThe residue was recrystallized from ethyl acetate-methanol
Sources & evidence
- ORD record
- ord-ca53b8459030424bae5304057d240603
- Source dataset
- uspto-grants-2001_07
- Patent number
- US06268354B1
Reaction notes
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