反応式
CO[C:3]([CH:5]1[CH2:9][C:8](=[O:10])[N:7]([CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:6]1)=[O:4].[NH2:18][CH2:19][CH2:20][OH:21]>CO>[OH:21][CH2:20][CH2:19][NH:18][C:3]([CH:5]1[CH2:9][C:8](=[O:10])[N:7]([CH2:11][C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH2:6]1)=[O:4]参加物
実験手順
A mixture of 46.7 g (0.2 mole) of methyl-5-oxo-1-(phenylmethyl)-3-pyrrolidinecarboxylate (J. Org. Chem., 26, 1519 (1961)], 36.7 g (0.6 mole) 2-aminoethanol and 500 ml methanol were refluxed overnight. The reaction was cooled to room temperature and the solvent removed at reduced pressure. The residue was taken up in dichloromethane and extracted 3×100 ml 1 N sodium hydroxide. The aqueous layer was taken to pH 5, extracted 3×150 ml dichloromethane, then taken to pH 8 and again extracted 3×150 ml dichloromethane. The aqueous layer was concentrated at reduced pressure and the resulting slurry stirred in dichloromethane. The salts were filtered off. The combined organic layers were dried over magnesium sulfate, the solvent removed at reduced pressure to yield 47.9 g of N-(2-hydroxyethyl)-5-oxo-1-(phenylmethyl)-3-pyrrolidinecarboxamide as an oil. This was used in the next step without further purification.
後処理
- customthe solvent removed at reduced pressure
- extractionextracted 3×100 ml 1 N sodium hydroxide
- extractionextracted 3×150 ml dichloromethane
- extractionagain extracted 3×150 ml dichloromethane
- concentrationThe aqueous layer was concentrated at reduced pressure
- filtrationThe salts were filtered off
- dry with materialThe combined organic layers were dried over magnesium sulfate
- customthe solvent removed at reduced pressure
出典と根拠
- ORDレコード
- ord-0028cf40ed30490fb01a61e1b8f3ef59
- 出典データセット
- uspto-grants-1985_10
- 特許番号
- US04550104
関連ノート
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