反応式
Br[CH:2]([C:7]([O:9][CH3:10])=[O:8])[C:3]([O:5][CH3:6])=[O:4].[C:11]([O:15][C:16](=[O:27])[C@@H:17]1[CH2:21][CH2:20][CH2:19][N:18]1[C:22](=[O:26])[C@H:23]([CH3:25])[NH2:24])([CH3:14])([CH3:13])[CH3:12]>ClCCl>[C:11]([O:15][C:16](=[O:27])[C@@H:17]1[CH2:21][CH2:20][CH2:19][N:18]1[C:22](=[O:26])[C@H:23]([CH3:25])[NH:24][CH:2]([C:7]([O:9][CH3:10])=[O:8])[C:3]([O:5][CH3:6])=[O:4])([CH3:13])([CH3:12])[CH3:14]参加物
反応条件
- 温度
- 0 °C
実験手順
Dimethyl bromomalonate (6.6 ml.) was added to a stirred solution of L-alanyl-L-proline t-butyl ester (22.9 g.) in dichloromethane (40 ml.) which was cooled to 0° C., and the mixture was allowed to warm up to laboratory temperature and stirred at that temperature for 16 hours, then diluted with dichloromethane (150 ml.). The solution was washed successively twice with aqueous 0.5N-citric acid solution (150 ml. each time), water (200 ml.) and saturated aqueous sodium chloride solution (200 ml.), dried over magnesium sulphate and evaporated to dryness. The residue was purified by chromatography on a silica gel column using a 4:1 v/v mixture of dichloromethane and ethyl acetate as eluant, and there was thus obtained as an oil N-(dimethoxycarbonylmethyl)-L-alanyl-L-proline t-butyl ester.
後処理
- temperatureto warm up to laboratory temperature
- washThe solution was washed successively twice with aqueous 0.5N-citric acid solution (150 ml
- dry with materialeach time), water (200 ml.) and saturated aqueous sodium chloride solution (200 ml.), dried over magnesium sulphate
- customevaporated to dryness
- customThe residue was purified by chromatography on a silica gel column
- additiona 4:1 v/v mixture of dichloromethane and ethyl acetate as eluant
出典と根拠
- ORDレコード
- ord-9d1472b862584287938396040f14e3cd
- 出典データセット
- uspto-grants-1985_07
- 特許番号
- US04528282
関連ノート
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