4-Chloro-3-(trifluoromethyl)benzenesulfonyl Chloride → 4-chloro-N-[5-chloro-2-(methylthio)phenyl]-3-(trifluoromethyl)benzenesulfonamide
Reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([S:9][CH3:10])=[C:6]([CH:8]=1)[NH2:7].[Cl:11][C:12]1[CH:17]=[CH:16][C:15]([S:18](Cl)(=[O:20])=[O:19])=[CH:14][C:13]=1[C:22]([F:25])([F:24])[F:23]>>[Cl:11][C:12]1[CH:17]=[CH:16][C:15]([S:18]([NH:7][C:6]2[CH:8]=[C:2]([Cl:1])[CH:3]=[CH:4][C:5]=2[S:9][CH3:10])(=[O:19])=[O:20])=[CH:14][C:13]=1[C:22]([F:25])([F:23])[F:24]Participants
3
Procedure
Following General Procedure B, the title compound was prepared from 5-chloro-2-(methylthio)aniline and 4-chloro-3-(trifluoromethyl)benzene-1-sulfonyl chloride.
Sources & evidence
- ORD record
- ord-26ad25e545eb4293a86605bc2a3041dd
- Source dataset
- uspto-grants-2013_05
- Patent number
- US08450367B2
Reaction notes
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