Phenylmethanesulfonyl chloride → N-(1,2-Diphenyl-1H-benzimidazol-5-yl)benzenemethanesulfonamide
Reaction equation
[NH2:1][C:2]1[CH:22]=[CH:21][C:5]2[N:6]([C:15]3[CH:20]=[CH:19][CH:18]=[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.[C:23]1([CH2:29][S:30](Cl)(=[O:32])=[O:31])[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1>>[C:15]1([N:6]2[C:5]3[CH:21]=[CH:22][C:2]([NH:1][S:30]([CH2:29][C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=4)(=[O:32])=[O:31])=[CH:3][C:4]=3[N:8]=[C:7]2[C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1Participants
3
Procedure
5-Amino-1,2-diphenyl-1H-benzimidazole was reacted with benzenemethanesulfonic acid chloride according to general operating instructions 13.
Sources & evidence
- ORD record
- ord-85d87976be814781bc312848f667e505
- Source dataset
- uspto-grants-2006_10
- Patent number
- US07115645B2
Reaction notes
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