Hydrochloric Acid → N-allyl-L-aspartic acid di-tert-butyl ester hydrochloride
反応式
[C:1]([O:5][C:6](=[O:20])[C@H:7]([CH2:12][C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[NH:8][CH2:9][CH:10]=[CH2:11])([CH3:4])([CH3:3])[CH3:2].O.[ClH:22]>C(#N)C>[ClH:22].[C:1]([O:5][C:6](=[O:20])[C@H:7]([CH2:12][C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[NH:8][CH2:9][CH:10]=[CH2:11])([CH3:4])([CH3:2])[CH3:3]参加物
5
実験手順
The obtained N-allyl-L-aspartic acid di-tert-butyl ester was dissolved in acetonitrile (10 mL), and water (17 mL) and 1N hydrochloric acid (1.8 mL, 1.8 mmol) were added. The solution was concentrated under reduced pressure and freeze-dried to give the title compound (0.54 g, 1.7 mmol, 47%).
後処理
- concentrationThe solution was concentrated under reduced pressure
- customfreeze-dried
出典と根拠
- ORDレコード
- ord-c243ac4b318141559b52fc26600362bd
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08877805B2
反応ノート
読み込み中…