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
To the compound (0.50 g, 1.8 mmol) obtained in step 1 were added water (17 mL) and 1N hydrochloric acid (1.8 mL, 1.8 mmol). Acetonitrile (10 ml) was added to dissolve the mixture, and the solution was concentrated under reduced pressure, and lyophilized to give the title compound (0.54 g, 1.7 mmol, 95%).
後処理
- dissolutionto dissolve the mixture
- concentrationthe solution was concentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-9c7fe5a3e3b24d4d85ca86f0be782854
- 出典データセット
- uspto-grants-2016_05
- 特許番号
- US09346821B2
反応ノート
読み込み中…