Hydrochloric Acid → HCID 11716529、化合物
反応式
[NH2:1][C@@H:2]([CH2:6][O:7][C:8]([O:10][C:11]1[C:16]([CH:17]([CH3:19])[CH3:18])=[CH:15][CH:14]=[CH:13][C:12]=1[CH:20]([CH3:22])[CH3:21])=[O:9])[C:3]([OH:5])=[O:4].[ClH:23]>>[NH2:1][C@@H:2]([CH2:6][O:7][C:8]([O:10][C:11]1[C:16]([CH:17]([CH3:18])[CH3:19])=[CH:15][CH:14]=[CH:13][C:12]=1[CH:20]([CH3:22])[CH3:21])=[O:9])[C:3]([OH:5])=[O:4].[ClH:23].[NH2:1][C@@H:2]([CH2:6][O:7][C:8]([O:10][C:11]1[C:16]([CH:17]([CH3:18])[CH3:19])=[CH:15][CH:14]=[CH:13][C:12]=1[CH:20]([CH3:22])[CH3:21])=[O:9])[C:3]([OH:5])=[O:4]参加物
4
実験手順
The hydrochloride salt of (S)-2-amino-3-(2,6-diisopropylphenoxycarbonyloxy)-propanoic acid was prepared by dissolving compound (3) in excess aqueous 1 N hydrochloric acid solution, freezing and then lyophilizing the solution to afford the desired product as an amorphous white solid.
出典と根拠
- ORDレコード
- ord-03dca5fac796452e892a3d13b075cca7
- 出典データセット
- uspto-grants-2009_11