Sodium Hydroxide → HCID 14071510, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([NH:11][CH:12]2[CH2:20][C:19]3[C:14](=[CH:15][CH:16]=[C:17]([C:21](=[O:28])[CH2:22][CH2:23][C:24]([O:26]C)=[O:25])[CH:18]=3)[CH2:13]2)(=[O:10])=[O:9])=[CH:4][CH:3]=1.[OH-].[Na+]>>[F:1][C:2]1[CH:3]=[CH:4][C:5]([S:8]([NH:11][CH:12]2[CH2:20][C:19]3[C:14](=[CH:15][CH:16]=[C:17]([C:21](=[O:28])[CH2:22][CH2:23][C:24]([OH:26])=[O:25])[CH:18]=3)[CH2:13]2)(=[O:10])=[O:9])=[CH:6][CH:7]=1Participants
3
Procedure
Prepared analogously to Example 2 from methyl 4-(2-p-fluorobenzenesulphonamido-indan-5-yl)-4-oxobutyrate by hydrolysis with sodium hydroxide.
Sources & evidence
- ORD record
- ord-aad639d265164f7582719b7f1f513336
- Source dataset
- uspto-grants-1990_05
- Patent number
- US04929754
Reaction notes
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