反応式
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[OH:12])[O:8][CH2:7][CH2:6][CH:5]2[C:13]([O:15][CH2:16][CH3:17])=[O:14].Cl[C:19]1[CH:27]=[CH:26][C:22]([C:23]([NH2:25])=[O:24])=[CH:21][C:20]=1[N+:28]([O-:30])=[O:29].C(=O)([O-])[O-].[K+].[K+]>CN(C=O)C>[C:23]([C:22]1[CH:26]=[CH:27][C:19]([O:12][C:11]2[CH:10]=[C:9]3[C:4]([CH:5]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH2:6][CH2:7][O:8]3)=[CH:3][C:2]=2[Cl:1])=[C:20]([N+:28]([O-:30])=[O:29])[CH:21]=1)(=[O:24])[NH2:25]参加物
反応条件
- 温度
- 90 °C
実験手順
To a stirred solution of ethyl 6-chloro-7-hydroxychroman-4-carboxylate (6.40 g, 24.9 mmol) and 4-chloro-3-nitrobenzamide in N,N′-dimethylformamide (75 mL) at ambient temperature was added potassium carbonate (8.61 g, 62.3 mmol). An argon balloon with purge valve was attached, and the stirred mixture was evacuated and purged 5 times with argon. The mixture was stirred in an oil bath at 90° C. under argon. After 15 hours the reaction mixture was cooled to ambient temperature, then poured into a reparatory funnel containing water (1000 mL) and the extracted with ether (2×1000 mL). The organic layers were combined and dried over sodium sulfate, then evaporated to give 10.5 g of brown semi-solid. The crude material was purified by silica gel column chromatography, eluting with 99/1 chloroform/methanol followed by 98/2 chloroform/methanol to provide the desired product (7.74 g, 74%).
後処理
- customAn argon balloon with purge valve
- customthe stirred mixture was evacuated
- custompurged 5 times with argon
- temperatureAfter 15 hours the reaction mixture was cooled to ambient temperature
- additionpoured into a reparatory funnel
- additioncontaining water (1000 mL)
- extractionthe extracted with ether (2×1000 mL)
- dry with materialdried over sodium sulfate
- customevaporated
出典と根拠
- ORDレコード
- ord-c1b39eb3f70f440594d30dc1127ef034
- 出典データセット
- uspto-grants-2014_07
- 特許番号
- US08785445B2
関連ノート
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