4-Chlorobenzenesulfonyl chloride → HCID 21938057, compound
Reaction equation
[NH2:1][C:2]1[CH:24]=[CH:23][C:5]2[N:6]([C:15]3[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=3)[C:7]([C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=3)=[N:8][C:4]=2[CH:3]=1.[Cl:25][C:26]1[CH:31]=[CH:30][C:29]([S:32](Cl)(=[O:34])=[O:33])=[CH:28][CH:27]=1>>[Cl:25][C:26]1[CH:31]=[CH:30][C:29]([S:32]([NH:1][C:2]2[CH:24]=[CH:23][C:5]3[N:6]([C:15]4[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=4)[C:7]([C:9]4[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=4)=[N:8][C:4]=3[CH:3]=2)(=[O:34])=[O:33])=[CH:28][CH:27]=1Participants
3
Procedure
5-Amino-1-(4-methoxyphenyl)-2-phenyl-1H-benzimidazole was reacted with 4-chlorobenzenesulfonic acid chloride according to general operating instructions 13.
Sources & evidence
- ORD record
- ord-fc4476f4545c4a7ab41d2536cbd9764d
- Source dataset
- uspto-grants-2008_03
- Patent number
- US07345075B2
Reaction notes
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