Ethyl 4-chlorobenzoate → HCID 13393254、化合物
反応式
[Cl:1][C:2]1[CH:12]=[CH:11][C:5]([C:6]([O:8]CC)=O)=[CH:4][CH:3]=1.CC[O-].[Na+].Cl.[NH2:18][CH:19]([CH2:23][CH:24]1[C:32]2[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=2)[NH:26][C:25]1=[O:33])[C:20]([OH:22])=[O:21]>C(O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([NH:18][CH:19]([CH2:23][CH:24]2[C:32]3[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=3)[NH:26][C:25]2=[O:33])[C:20]([OH:22])=[O:21])=[O:8])=[CH:11][CH:12]=1参加物
実験手順
In 100 ml of ethanol, 1.66 g of ethyl p-chlorobenzoate, 0.5 g of sodium ethylate and 1.98 g of 2-amino-3-(oxindol-3-yl)propionic acid hydrochloride prepared in Reference example 1 were added, then the mixture was placed in an autoclave, and reacted under 110 atmospheric pressure at 140°-150° C. for 6 hours. After cooling, the reaction mixture was concentrated under a reduced pressure, the residue was dissolved in 200 ml of chloroform, then the chloroform solution was washed with 1% potassium carbonate aqueous solution, diluted hydrochloric acid and water in this order, the chloroform solution was dried with anhydrous sodium sulfate. The solvent was removed by evaporation, the residue was recrystallized from methanol-water to obtain 270 mg of 2-(4-chlorobenzoylamino)-3-(oxindol-3-yl)propionic acid 1/4-hydrate in the form of colorless powdery substance. Melting point: 133-135° C. [α]D25 -50.3° (C=1, methanol)
後処理
- additionwere added
- customreacted under 110 atmospheric pressure at 140°-150° C. for 6 hours
- temperatureAfter cooling
- concentrationthe reaction mixture was concentrated under a reduced pressure
- dissolutionthe residue was dissolved in 200 ml of chloroform
- washthe chloroform solution was washed with 1% potassium carbonate aqueous solution, diluted hydrochloric acid and water in this order
- dry with materialthe chloroform solution was dried with anhydrous sodium sulfate
- customThe solvent was removed by evaporation
- customthe residue was recrystallized from methanol-water
出典と根拠
- ORDレコード
- ord-f20c269618634eb28d7defb1578ecbce
- 出典データセット
- uspto-grants-1987_09
- 特許番号
- US04694017
反応ノート
読み込み中…