4-Toluenesulfonyl chloride → HCID 22617826, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6](=[O:11])[C:5]2=[O:12].[C:13]1([CH3:23])[CH:18]=[CH:17][C:16]([S:19](Cl)(=[O:21])=[O:20])=[CH:15][CH:14]=1>>[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([S:19]([C:16]1[CH:17]=[CH:18][C:13]([CH3:23])=[CH:14][CH:15]=1)(=[O:21])=[O:20])[C:6](=[O:11])[C:5]2=[O:12]Participants
3
Procedure
5-chloro-N-(p-tolylsulfonyl)-isatin was prepared by the method of Example 3, Step B from 5-chloroisatin and p-tolylsulfonyl chloride.
Sources & evidence
- ORD record
- ord-76930da0dd4a47658b06764d10986f42
- Source dataset
- uspto-grants-2002_04
- Patent number
- US06372742B1
Reaction notes
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