Sodium Hydroxide → 3-Methyl-4-(2-benzenesulphonamido-indan-5-yl)-4-oxobutyric acid
Reaction equation
[CH3:1][CH:2]([C:8]([C:10]1[CH:11]=[C:12]2[C:16](=[CH:17][CH:18]=1)[CH2:15][CH:14]([NH:19][S:20]([C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)(=[O:22])=[O:21])[CH2:13]2)=[O:9])[CH2:3][C:4]([O:6]C)=[O:5].[OH-].[Na+]>>[CH3:1][CH:2]([C:8]([C:10]1[CH:11]=[C:12]2[C:16](=[CH:17][CH:18]=1)[CH2:15][CH:14]([NH:19][S:20]([C:23]1[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=1)(=[O:22])=[O:21])[CH2:13]2)=[O:9])[CH2:3][C:4]([OH:6])=[O:5]Participants
3
Procedure
Prepared analogously to Example 2 from methyl 3-methyl-4-(2-benzenesulphonamido-indan-5-yl)-4-oxobutyrate by hydrolysis with sodium hydroxide.
Sources & evidence
- ORD record
- ord-568d46e91e5545678e78cbe4b288f2d1
- Source dataset
- uspto-grants-1990_05
- Patent number
- US04929754
Reaction notes
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