p-Toluidine → HCID 58978407, compound
Reaction equation
Br[CH2:2][C:3](Br)=[O:4].[CH2:6]([NH:8][CH2:9][CH3:10])[CH3:7].[NH2:11][C:12]1[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=1.[F:19][C:20]([F:32])([F:31])[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=1[S:27](Cl)(=[O:29])=[O:28]>>[CH2:6]([N:8]([CH2:9][CH3:10])[C:3](=[O:4])[CH2:2][N:11]([C:12]1[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=1)[S:27]([C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][C:21]=1[C:20]([F:19])([F:31])[F:32])(=[O:29])=[O:28])[CH3:7]Participants
5
Procedure
prepared by reaction of 2-bromoacetyl bromide with diethylamine, p-toluidine and 2-trifluoromethyl-benzenesulfonyl chloride
Sources & evidence
- ORD record
- ord-e9e6496ca5c04a17a3b21678dae54e47
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435815B2
Reaction notes
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