Citric Acid → HCID 67491029、化合物
反応式
[BH4-].[Na+].[C:3]([O:7][C:8]([C@@:10]1([CH2:24][CH:25]=[O:26])[CH2:14][C:13](=[O:15])[N:12]([C@@H:16]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH3:17])[CH2:11]1)=[O:9])([CH3:6])([CH3:5])[CH3:4].C(O)(=O)CC(CC(O)=O)(C(O)=O)O.C(OCC)(=O)C>CO>[C:3]([O:7][C:8]([C@@:10]1([CH2:24][CH2:25][OH:26])[CH2:14][C:13](=[O:15])[N:12]([C@@H:16]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH3:17])[CH2:11]1)=[O:9])([CH3:6])([CH3:5])[CH3:4]参加物
実験手順
Sodium borohydride (465 mg) was added to a solution of (3S)-5-oxo-3-(2-oxoethyl)-1-[(1R)-1-phenylethyl]pyrrolidine-3-carboxylic acid tert-butyl ester (2.71 g, 8.19 mmol) in methanol at −40° C. After heating to room temperature, a 10% citric acid solution was added to the reaction solution, and the mixture was stirred. The reaction solution was poured into a mixture of ethyl acetate (50 mL) and a 10% citric acid solution (10 mL), followed by extraction with ethyl acetate (100 mL). The aqueous layer was extracted with ethyl acetate (100 mL), and then the organic layers were combined and washed with brine (50 mL×2). The resulting organic layer was dried over anhydrous sodium sulfate and filtered, and then the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=2:1→1:1→0:1→ethyl acetate-methanol=10:1) to give 2.20 g (81%) of the title compound as a white solid.
後処理
- extractiona 10% citric acid solution (10 mL), followed by extraction with ethyl acetate (100 mL)
- extractionThe aqueous layer was extracted with ethyl acetate (100 mL)
- washwashed with brine (50 mL×2)
- dry with materialThe resulting organic layer was dried over anhydrous sodium sulfate
- filtrationfiltered
- concentrationthe filtrate was concentrated under reduced pressure
- customThe resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=2:1→1:1→0:1→ethyl acetate-methanol=10:1)
出典と根拠
- ORDレコード
- ord-b372ebc824904632aa04cdde1ef5edd4
- 出典データセット
- uspto-grants-2013_12
- 特許番号
- US08618094B2
反応ノート
読み込み中…