HCID 11172445, compound → HCID 86607726, compound
Reaction equation
[CH:1]([C:3]1[CH:4]=[C:5]([S:20]([NH2:23])(=[O:22])=[O:21])[CH:6]=[C:7]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([N+:17]([O-:19])=[O:18])[CH:12]=2)[C:8]=1[O:9][CH3:10])=[O:2].[Cl:24][C:25]1[CH:26]=[C:27]([CH2:32][CH2:33][C:34](Cl)=[O:35])[CH:28]=[CH:29][C:30]=1[Cl:31]>>[Cl:24][C:25]1[CH:26]=[C:27]([CH2:32][CH2:33][C:34]([NH:23][S:20]([C:5]2[CH:6]=[C:7]([C:11]3[CH:16]=[CH:15][CH:14]=[C:13]([N+:17]([O-:19])=[O:18])[CH:12]=3)[C:8]([O:9][CH3:10])=[C:3]([CH:1]=[O:2])[CH:4]=2)(=[O:22])=[O:21])=[O:35])[CH:28]=[CH:29][C:30]=1[Cl:31]Participants
3
Procedure
Proceeding as in Reference 21, but substituting 5-formyl-6-methoxy-3′-nitro-biphenyl-3-sulfonamide and 3-(3,4-dichlorophenyl)-propanoyl chloride, gave N-[3-(3,4-dichlorophenyl)-propanoyl]-5-formyl-6-methoxy-3′-nitro-biphenyl-3-sulfonamide.
Sources & evidence
- ORD record
- ord-b7b233f9ebaf45c6babb2e73940aca45
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08778625B2
Reaction notes
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