2-Thiophenesulfonyl chloride → N-[5-chloro-2-(methylthio)phenyl]thiophene-2-sulfonamide
Reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([S:9]([CH3:11])=O)=[C:6]([CH:8]=1)[NH2:7].[S:12]1[CH:16]=[CH:15][CH:14]=[C:13]1[S:17](Cl)(=[O:19])=[O:18]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([S:9][CH3:11])=[C:6]([NH:7][S:17]([C:13]2[S:12][CH:16]=[CH:15][CH:14]=2)(=[O:19])=[O:18])[CH:8]=1Participants
3
Procedure
Following General Procedure B, the title compound was prepared from 5-chloro-2-(methylsulfinyl)aniline and thiophene-2-sulfonyl chloride.
Sources & evidence
- ORD record
- ord-2174c25f59674864bf40eea433a4b61e
- Source dataset
- uspto-grants-2014_11
- Patent number
- US08877804B2
Reaction notes
Loading…