4-t-Butylbenzenesulfonyl chloride → 4-tert-Butyl-N-(6-methyl-3-pyridinyl)benzenesulfonamide
Reaction equation
[CH3:1][C:2]1[N:7]=[CH:6][C:5]([NH2:8])=[CH:4][CH:3]=1.[C:9]([C:13]1[CH:18]=[CH:17][C:16]([S:19](Cl)(=[O:21])=[O:20])=[CH:15][CH:14]=1)([CH3:12])([CH3:11])[CH3:10]>>[C:9]([C:13]1[CH:18]=[CH:17][C:16]([S:19]([NH:8][C:5]2[CH:6]=[N:7][C:2]([CH3:1])=[CH:3][CH:4]=2)(=[O:21])=[O:20])=[CH:15][CH:14]=1)([CH3:12])([CH3:10])[CH3:11]Participants
3
Procedure
prepared by reaction of 6-methyl-pyridin-3-ylamine with 4-tert-butyl-benzene-sulfonyl chloride
Sources & evidence
- ORD record
- ord-d7b3007cfcd241bcb90bd84cd1ab1ad6
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435815B2
Reaction notes
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