反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][NH:6][C:5](=[O:9])[C:4]=1[C:10]#[N:11].[F:12][C:13]1[CH:14]=[C:15]([CH:18]=[C:19]([F:22])[C:20]=1F)[C:16]#[N:17].C(=O)([O-])[O-].[K+].[K+].C(=O)([O-])O.[Na+]>CN(C)C=O>[C:16]([C:15]1[CH:14]=[C:13]([F:12])[C:20]([N:6]2[CH:7]=[CH:8][C:3]([O:2][CH3:1])=[C:4]([C:10]#[N:11])[C:5]2=[O:9])=[C:19]([F:22])[CH:18]=1)#[N:17]参加物
6
反応条件
- 温度
- 50 °C
実験手順
A mixture of 4-methoxy-2-oxo-1,2-dihydropyridine-3-carbonitrile (2.00 g), 3,4,5-trifluorobenzonitrile (2.93 g), potassium carbonate (3.68 g) and N,N-dimethylformamide (20 mL) was stirred at 50° C. for 5 hr. The reaction mixture was slowly poured into saturated sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. To the residue was added a mixed solvent (10 mL) of isopropyl ether/ethyl acetate=4/1, and the mixture was stirred for 15 min. The precipitate was collected by filtration to give the title compound (1.65 g).
後処理
- extractionthe mixture was extracted with ethyl acetate
- washThe extract was washed with saturated brine
- dry with materialdried over anhydrous magnesium sulfate
- customthe solvent was evaporated under reduced pressure
- additionTo the residue was added a mixed solvent (10 mL) of isopropyl ether/ethyl acetate=4/1
- stirringthe mixture was stirred for 15 min
- filtrationThe precipitate was collected by filtration
出典と根拠
- ORDレコード
- ord-4a47bf8505ac4472bc43a66e5f332700
- 出典データセット
- uspto-grants-2015_07
- 特許番号
- US09085578B2
関連ノート
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