m-Toluidine → HCID 10004240, compound
Reaction equation
Br[CH2:2][C:3](Br)=[O:4].[CH:6]1([CH2:9][NH:10][CH2:11][CH2:12][CH3:13])[CH2:8][CH2:7]1.[NH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([CH3:21])[CH:16]=1.[C:22]([C:26]1[CH:31]=[CH:30][C:29]([S:32](Cl)(=[O:34])=[O:33])=[CH:28][CH:27]=1)([CH3:25])([CH3:24])[CH3:23]>>[C:22]([C:26]1[CH:31]=[CH:30][C:29]([S:32]([N:14]([C:15]2[CH:16]=[C:17]([CH3:21])[CH:18]=[CH:19][CH:20]=2)[CH2:2][C:3]([N:10]([CH2:9][CH:6]2[CH2:8][CH2:7]2)[CH2:11][CH2:12][CH3:13])=[O:4])(=[O:34])=[O:33])=[CH:28][CH:27]=1)([CH3:25])([CH3:23])[CH3:24]Participants
5
Procedure
prepared by reaction of 2-bromoacetyl bromide with N-cyclopropylmethyl-N-propylamine, m-toluidine and 4-tert-butyl-benzenesulfonyl chloride
Sources & evidence
- ORD record
- ord-ffe0376e2f4948d78cf09b645580fc5a
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435815B2
Reaction notes
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