2-Naphthalenesulfonyl chloride → HCID 58978374, 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.[CH:19]1[C:28]2[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=2)[CH:22]=[CH:21][C:20]=1[S:29](Cl)(=[O:31])=[O:30]>>[CH2:6]([N:8]([CH2:9][CH3:10])[C:3](=[O:4])[CH2:2][N:11]([S:29]([C:20]1[CH:21]=[CH:22][C:23]2[C:28](=[CH:27][CH:26]=[CH:25][CH:24]=2)[CH:19]=1)(=[O:31])=[O:30])[C:12]1[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=1)[CH3:7]Participants
5
Procedure
prepared by reaction of 2-bromoacetyl bromide with diethylamine, p-toluidine and 2-naphthalenesulfonyl chloride
Sources & evidence
- ORD record
- ord-913110c3af784dd0b3a9114b52d031a9
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435815B2
Reaction notes
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