p-Toluidine → HCID 58978401, compound
Reaction equation
Br[CH2:2][C:3](Br)=[O:4].[CH2:6]([NH:8][CH3:9])[CH3:7].[NH2:10][C:11]1[CH:16]=[CH:15][C:14]([CH3:17])=[CH:13][CH:12]=1.[C:18]([C:22]1[CH:27]=[CH:26][C:25]([S:28](Cl)(=[O:30])=[O:29])=[CH:24][CH:23]=1)([CH3:21])([CH3:20])[CH3:19]>>[C:18]([C:22]1[CH:27]=[CH:26][C:25]([S:28]([N:10]([C:11]2[CH:16]=[CH:15][C:14]([CH3:17])=[CH:13][CH:12]=2)[CH2:2][C:3]([N:8]([CH2:6][CH3:7])[CH3:9])=[O:4])(=[O:30])=[O:29])=[CH:24][CH:23]=1)([CH3:21])([CH3:19])[CH3:20]Participants
5
Procedure
prepared by reaction of 2-bromoacetyl bromide with ethylmethylamine, p-toluidine and 4-tert-butyl-benzenesulfonyl chloride
Sources & evidence
- ORD record
- ord-0cb4c9df706341f5b9f7c81ad4e96d18
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435815B2
Reaction notes
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