1H-Indazol-6-amine → 4-tert-Butyl-N-(1H-indazol-6-yl)-benzenesulfonamide
Reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([NH2:10])[CH:8]=2)[CH:3]=[N:2]1.[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:10][C:7]2[CH:8]=[C:9]3[C:4]([CH:3]=[N:2][NH:1]3)=[CH:5][CH:6]=2)(=[O:23])=[O:22])=[CH:17][CH:16]=1)([CH3:14])([CH3:12])[CH3:13]Participants
3
Procedure
prepared by reaction of 1H-indazol-6-ylamine with 4-tert-butyl-benzenesulfonyl chloride
Sources & evidence
- ORD record
- ord-cb1309d9c1b247c0b54a6f92d349650b
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435815B2
Reaction notes
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