反応式
[SH:1][C:2]([CH3:13])([CH3:12])[C:3]([NH:5][C@H:6]([C:9]([OH:11])=[O:10])[CH2:7][SH:8])=[O:4].[C:14](O)(=O)C>CCOCC.[N+](=C)=[N-]>[CH3:14][O:10][C:9](=[O:11])[C@H:6]([CH2:7][SH:8])[NH:5][C:3](=[O:4])[C:2]([SH:1])([CH3:13])[CH3:12]参加物
5
実験手順
To a solution of N-(2-mercapto-2-methylpropionyl)-L-cysteine (1.0 g) in ether(3 ml), diazomethane dissolved in ether(12 ml) was added dropwise under ice-cooling. After the addition, acetic acid was added to the reaction mixture. The reaction mixture was washed with saturated sodium hydrogen carbonate solution and saturated sodium chloride solution, dried over anhydrous sodium sulfate and concentrated in vacuo. The oily residue was purified by a silica gel column chromatography to give 1.0 g(94%) of the titled compound.
後処理
- additionwas added dropwise under ice-
- temperaturecooling
- additionwas added to the reaction mixture
- washThe reaction mixture was washed with saturated sodium hydrogen carbonate solution and saturated sodium chloride solution
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated in vacuo
- customThe oily residue was purified by a silica gel column chromatography
出典と根拠
- ORDレコード
- ord-d22ad1ba57f24a5b9ffc12e56b23c69d
- 出典データセット
- uspto-grants-1994_03
- 特許番号
- US05292926
関連ノート
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