4-(Trifluoromethyl)benzenesulfonyl chloride → HCID 58727984, compound
Reaction equation
[CH3:1][C:2]([CH3:18])([C:6](=[O:17])[NH:7][S:8]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)(=[O:10])=[O:9])[C:3]([OH:5])=[O:4].[F:19][C:20]([F:32])([F:31])C1C=CC(S(Cl)(=O)=O)=CC=1>>[CH3:1][C:2]([CH3:18])([C:6](=[O:17])[NH:7][S:8]([C:11]1[CH:16]=[CH:15][C:14]([C:20]([F:32])([F:31])[F:19])=[CH:13][CH:12]=1)(=[O:10])=[O:9])[C:3]([OH:5])=[O:4]Participants
3
Procedure
2,2-dimethyl-3-oxo-3-({[4-(trifluoromethyl)phenyl]sulfonyl}amino)propanoic acid was prepared in the same manner as 2,2-dimethyl-3-oxo-3-[(phenylsulfonyl)amino]propanoic acid starting from 4-(trifluoromethyl)benzenesulfonyl chloride.
Sources & evidence
- ORD record
- ord-b376943d603a46bc9e3d9cb5430073b5
- Source dataset
- uspto-grants-2010_01
- Patent number
- US07645771B2
Reaction notes
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