Sodium Hydroxide → 4-(2-o-Methoxybenzenesulphonamido-indan-5-yl)-4-oxobutyric acid
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[S:9]([NH:12][CH:13]1[CH2:21][C:20]2[C:15](=[CH:16][CH:17]=[C:18]([C:22](=[O:29])[CH2:23][CH2:24][C:25]([O:27]C)=[O:26])[CH:19]=2)[CH2:14]1)(=[O:11])=[O:10].[OH-].[Na+]>>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[S:9]([NH:12][CH:13]1[CH2:21][C:20]2[C:15](=[CH:16][CH:17]=[C:18]([C:22](=[O:29])[CH2:23][CH2:24][C:25]([OH:27])=[O:26])[CH:19]=2)[CH2:14]1)(=[O:10])=[O:11]Participants
3
Procedure
Prepared analogously to Example 2 from methyl 4-(2-o-methoxybenzenesulphonamido-indan-5-yl)-4-oxobuty rate by hydrolysis with sodium hydroxide.
Sources & evidence
- ORD record
- ord-161cb8235749432a9777f39de22b2693
- Source dataset
- uspto-grants-1989_04