反応式
[H-].[Na+].C([O:5][C:6](=O)[CH2:7][CH2:8][C:9]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[NH2:17])=[O:10])C.O>C1COCC1>[NH:17]1[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[C:9](=[O:10])[CH2:8][CH2:7][C:6]1=[O:5]参加物
5
実験手順
To a suspension of sodium hydride (10 mg, 0.43 mmol) in dry THF (1 mL) was added 4-(2-amino-phenyl)-4-oxo-butyric acid ethyl ester (80 mg, 0.36 mmol) under Argon at −40° C. The reaction mixture was then allowed to warm up to rt over 3 h, and then added to water (20 mL). The mixture was then extracted with DCM (3×15 mL) and the combined extracts were then dried (sodium sulfate), and evaporated to leave an off-white solid. Recrystallization from EtOAc afforded a white solid (51 mg, 81%), m/z 175 (M).
後処理
- extractionThe mixture was then extracted with DCM (3×15 mL)
- dry with materialthe combined extracts were then dried (sodium sulfate)
- customevaporated
- customto leave an off-white solid
- customRecrystallization from EtOAc
出典と根拠
- ORDレコード
- ord-5ea0ac506de94e1ca90453849bbf16c6
- 出典データセット
- uspto-grants-2004_02
- 特許番号
- US06686352B2
関連ノート
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