Benzenepropanoyl chloride → HCID 86628078, compound
Reaction equation
[CH:1]([C:3]1[CH:4]=[C:5]([S:17]([NH2:20])(=[O:19])=[O:18])[CH:6]=[C:7]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[C:8]=1[O:9][CH3:10])=[O:2].[C:21]1([CH2:27][CH2:28][C:29](Cl)=[O:30])[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>>[CH:1]([C:3]1[CH:4]=[C:5]([S:17]([NH:20][C:29](=[O:30])[CH2:28][CH2:27][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)(=[O:19])=[O:18])[CH:6]=[C:7]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[C:8]=1[O:9][CH3:10])=[O:2]Participants
3
Procedure
Proceeding as in Reference 21, but substituting 5-formyl-6-methoxy-biphenyl-3-sulfonamide and 3-phenyl-propanoyl chloride, gave 5-formyl-6-methoxy-N-(3-phenyl-propanoyl)-biphenyl-3-sulfonamide.
Sources & evidence
- ORD record
- ord-8e54c72e374644199afb7afc7442c0ee
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08778625B2
Reaction notes
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