Bromoacetyl bromide → HCID 10435642, compound
Reaction equation
Br[CH2:2][C:3](Br)=[O:4].[CH2:6]([NH:13][CH2:14][CH3:15])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[CH3:16][O:17][C:18]1[N:23]=[CH:22][C:21]([NH:24][S:25]([C:28]2[CH:37]=[CH:36][C:35]3[C:30](=[CH:31][CH:32]=[CH:33][CH:34]=3)[CH:29]=2)(=[O:27])=[O:26])=[CH:20][CH:19]=1>>[CH2:6]([N:13]([CH2:14][CH3:15])[C:3](=[O:4])[CH2:2][N:24]([C:21]1[CH:22]=[N:23][C:18]([O:17][CH3:16])=[CH:19][CH:20]=1)[S:25]([C:28]1[CH:37]=[CH:36][C:35]2[C:30](=[CH:31][CH:32]=[CH:33][CH:34]=2)[CH:29]=1)(=[O:26])=[O:27])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1Participants
4
Procedure
prepared by reaction of 2-bromoacetyl bromide with N-benzyl-N-ethylamine and naphthalene-2-sulfonic acid (6-methoxy-pyridin-3-yl)-amide
Sources & evidence
- ORD record
- ord-0bc69bda9ad44ab4be4facf4225bced0
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435815B2
Reaction notes
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