Potassium Carbonate → N-Isoamyl-N-(6-hydroxy naphthalene-2-sulfonyl)-D-valine tert-butyl ester
反応式
[C:1]([O:5][C:6](=[O:34])[C@@H:7]([CH:31]([CH3:33])[CH3:32])[N:8]([CH2:26][CH2:27][CH:28]([CH3:30])[CH3:29])[S:9]([C:12]1[CH:21]=[CH:20][C:19]2[C:14](=[CH:15][CH:16]=[C:17]([O:22]C(=O)C)[CH:18]=2)[CH:13]=1)(=[O:11])=[O:10])([CH3:4])([CH3:3])[CH3:2].C(=O)([O-])[O-].[K+].[K+]>C(O)C.O>[C:1]([O:5][C:6](=[O:34])[C@@H:7]([CH:31]([CH3:33])[CH3:32])[N:8]([CH2:26][CH2:27][CH:28]([CH3:29])[CH3:30])[S:9]([C:12]1[CH:21]=[CH:20][C:19]2[C:14](=[CH:15][CH:16]=[C:17]([OH:22])[CH:18]=2)[CH:13]=1)(=[O:11])=[O:10])([CH3:3])([CH3:4])[CH3:2]参加物
4
実験手順
To a solution of N-isoamyl-N-(6-acetoxy naphthalene-2-sulfonyl)-D-valine tert-butyl ester (0.75 g, 1.53 mmol) in ethanol-water (35 mL-15 mL) is added potassium carbonate (0.422 g, 3.05 mmol), and the reaction is heated to reflux for 16 h. The solvents are removed in vacuo, and the residue is redissolved in water and extracted three times with dichloromethane. The combined organic extracts are washed with sodium bicarbonate and brine, dried over sodium sulfate, and concentrated in vacuo. The crude product is purified by column chromatography (10% hexanes-ethyl acetate) to afford the title compound as a yellow oil (0.58 g, 85% yield).
後処理
- temperaturethe reaction is heated
- temperatureto reflux for 16 h
- customThe solvents are removed in vacuo
- dissolutionthe residue is redissolved in water
- extractionextracted three times with dichloromethane
- washThe combined organic extracts are washed with sodium bicarbonate and brine
- dry with materialdried over sodium sulfate
- concentrationconcentrated in vacuo
- customThe crude product is purified by column chromatography (10% hexanes-ethyl acetate)
出典と根拠
- ORDレコード
- ord-7a774f54f8724fa78ecf6c8d08696d59
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08841291B2
反応ノート
読み込み中…