2,4-Dimethoxybenzylamine → HCID 22636362, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:10]=[C:9]([O:11][CH3:12])[CH:8]=[CH:7][C:4]=1[CH2:5][NH2:6].[Br:13][CH2:14][CH2:15][CH2:16][CH2:17][C:18]1([C:31](Cl)=[O:32])[C:30]2[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=2[C:24]2[C:19]1=[CH:20][CH:21]=[CH:22][CH:23]=2>>[CH3:1][O:2][C:3]1[CH:10]=[C:9]([O:11][CH3:12])[CH:8]=[CH:7][C:4]=1[CH2:5][NH:6][C:31]([C:18]1([CH2:17][CH2:16][CH2:15][CH2:14][Br:13])[C:30]2[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=2[C:24]2[C:19]1=[CH:20][CH:21]=[CH:22][CH:23]=2)=[O:32]Participants
3
Procedure
Prepared analogously to Example 1 from 2,4-dimethoxybenzylamine and 9-(4-bromo-butyl)-9H-fluorene-9-carboxylic acid chloride.
Sources & evidence
- ORD record
- ord-abaaefaf612d40e7a8c4861f4ca6eabe
- Source dataset
- uspto-grants-2004_11
- Patent number
- US06821967B2
Reaction notes
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