p-Toluidine → N,N-Diethyl-2-[(4-isopropyl-benzenesulfonyl)-p-tolyl-amino]-acetamide
Reaction equation
Br[CH2:2][C:3]([N:5]([CH2:8][CH3:9])[CH2:6][CH3:7])=[O:4].[NH2:10][C:11]1[CH:16]=[CH:15][C:14]([CH3:17])=[CH:13][CH:12]=1.[CH:18]([C:21]1[CH:26]=[CH:25][C:24]([S:27](Cl)(=[O:29])=[O:28])=[CH:23][CH:22]=1)([CH3:20])[CH3:19]>>[CH2:6]([N:5]([CH2:8][CH3:9])[C:3](=[O:4])[CH2:2][N:10]([S:27]([C:24]1[CH:25]=[CH:26][C:21]([CH:18]([CH3:20])[CH3:19])=[CH:22][CH:23]=1)(=[O:29])=[O:28])[C:11]1[CH:16]=[CH:15][C:14]([CH3:17])=[CH:13][CH:12]=1)[CH3:7]Participants
4
Procedure
prepared by reaction of 2-bromo-N,N-diethylacetamide with p-toluidine and 4-isopropyl-benzenesulfonyl chloride
Sources & evidence
- ORD record
- ord-33f06f46261c40359246bd025b3da1c3
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435815B2
Reaction notes
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