Benzylamine → HCID 18442598, compound
Reaction equation
Br[CH2:2][C:3](Br)=[O:4].[CH2:6]([NH2:13])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[CH3:14][O:15][C:16]1[CH:17]=[C:18]([CH:35]=[CH:36][C:37]=1[O:38][CH3:39])[CH2:19][CH:20]1[C:26]2[CH:27]=[C:28]([O:33][CH3:34])[C:29]([O:31][CH3:32])=[CH:30][C:25]=2[O:24][CH2:23][CH2:22][NH:21]1>>[CH2:6]([NH:13][C:3](=[O:4])[CH2:2][N:21]1[CH:20]([CH2:19][C:18]2[CH:35]=[CH:36][C:37]([O:38][CH3:39])=[C:16]([O:15][CH3:14])[CH:17]=2)[C:26]2[CH:27]=[C:28]([O:33][CH3:34])[C:29]([O:31][CH3:32])=[CH:30][C:25]=2[O:24][CH2:23][CH2:22]1)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1Participants
4
Procedure
prepared by reaction of 2-bromoacetyl bromide with benzylamine and 5-(3,4-dimethoxy-benzyl)-7,8-dimethoxy-2,3,4,5-tetrahydro-benzo[f][1,4]oxazepine.
Sources & evidence
- ORD record
- ord-7224279536714c2b97ad71b8d2f68dae
- Source dataset
- uspto-grants-2007_03
- Patent number
- US07192950B2
Reaction notes
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