Anthranilamide → 2-(4-Tert-butylbenzenesulfonamido)benzamide
Reaction equation
[NH2:1][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([NH2:6])=[O:5].[C:11]([C:15]1[CH:20]=[CH:19][C:18]([S:21](Cl)(=[O:23])=[O:22])=[CH:17][CH:16]=1)([CH3:14])([CH3:13])[CH3:12]>>[C:11]([C:15]1[CH:20]=[CH:19][C:18]([S:21]([NH:1][C:2]2[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=2[C:4]([NH2:6])=[O:5])(=[O:23])=[O:22])=[CH:17][CH:16]=1)([CH3:14])([CH3:12])[CH3:13]Participants
3
Procedure
prepared by reaction of 2-amino-benzamide with 4-tert-butyl-benzenesulfonyl chloride
Sources & evidence
- ORD record
- ord-7866b1bf610440bf90cda9b7b434319b
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435815B2
Reaction notes
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