Diethylamine → HCID 10048454, compound
Reaction equation
Br[CH2:2][C:3](Br)=[O:4].[CH2:6]([NH:8][CH2:9][CH3:10])[CH3:7].[CH3:11][O:12][C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([NH2:19])[CH:14]=1.[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:19]([C:15]2[CH:16]=[CH:17][CH:18]=[C:13]([O:12][CH3:11])[CH:14]=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, m-anisidine and 4-tert-butyl-benzenesulfonyl chloride
Sources & evidence
- ORD record
- ord-eb9ccd9ce50948e086748519fe8e7c6f
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435815B2
Reaction notes
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