Diethylamine → HCID 58978427, compound
Reaction equation
Br[CH2:2][C:3](Br)=[O:4].[CH2:6]([NH:8][CH2:9][CH3:10])[CH3:7].[CH2:11]([C:13]1[CH:19]=[CH:18][C:16]([NH2:17])=[CH:15][CH:14]=1)[CH3:12].[C:20]([C:24]1[CH:29]=[CH:28][C:27]([S:30](Cl)(=[O:32])=[O:31])=[CH:26][CH:25]=1)([CH3:23])([CH3:22])[CH3:21]>>[C:20]([C:24]1[CH:29]=[CH:28][C:27]([S:30]([N:17]([C:16]2[CH:18]=[CH:19][C:13]([CH2:11][CH3:12])=[CH:14][CH:15]=2)[CH2:2][C:3]([N:8]([CH2:9][CH3:10])[CH2:6][CH3:7])=[O:4])(=[O:32])=[O:31])=[CH:26][CH:25]=1)([CH3:23])([CH3:21])[CH3:22]Participants
5
Procedure
prepared by reaction of 2-bromoacetyl bromide with diethylamine, 4-ethylaniline and 4-tert-butyl-benzenesulfonyl chloride
Sources & evidence
- ORD record
- ord-251dec7f9fdc41afb320242d2df08aa4
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435815B2
Reaction notes
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