4-(Propan-2-yl)benzene-1-sulfonyl chloride → N-[4-bromo-2-(pyridine-4-carbonyl)-phenyl]-4-isopropyl-benzenesulfonamide
Reaction equation
[CH:1]([C:4]1[CH:9]=[CH:8][C:7]([S:10](Cl)(=[O:12])=[O:11])=[CH:6][CH:5]=1)([CH3:3])[CH3:2].[NH2:14][C:15]1[CH:20]=[CH:19][C:18]([Br:21])=[CH:17][C:16]=1[C:22]([C:24]1[CH:29]=[CH:28][N:27]=[CH:26][CH:25]=1)=[O:23]>>[Br:21][C:18]1[CH:19]=[CH:20][C:15]([NH:14][S:10]([C:7]2[CH:8]=[CH:9][C:4]([CH:1]([CH3:3])[CH3:2])=[CH:5][CH:6]=2)(=[O:12])=[O:11])=[C:16]([C:22]([C:24]2[CH:25]=[CH:26][N:27]=[CH:28][CH:29]=2)=[O:23])[CH:17]=1Participants
3
Procedure
The title compound was prepared according the general procedure for the synthesis of N-aryl-benzenesulfonamides using 4-isopropyl-benzenesulfonyl chloride and (2-amino-5-bromo-phenyl)-pyridin-4-yl-methanone and purified by HPLC. MS: m/z 460 (M++1).
Workup
- custompurified by HPLC
Sources & evidence
- ORD record
- ord-3eeab6dceb824ad49848c9a35c04e7be
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07420055B2
Reaction notes
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