2-Bromobenzoyl chloride → (2-Bromophenyl)-[3-hydroxy-3-(3-methoxyphenyl)-piperidine-1-yl]-methanone
Reaction equation
[Br:1][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4](Cl)=[O:5].[CH3:11][O:12][C:13]1[CH:14]=[C:15]([C:19]2([OH:25])[CH2:24][CH2:23][CH2:22][NH:21][CH2:20]2)[CH:16]=[CH:17][CH:18]=1>>[Br:1][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([N:21]1[CH2:22][CH2:23][CH2:24][C:19]([OH:25])([C:15]2[CH:16]=[CH:17][CH:18]=[C:13]([O:12][CH3:11])[CH:14]=2)[CH2:20]1)=[O:5]Participants
3
Procedure
The compound of Example 20 was prepared according to the general preparation protocol A from 2-bromobenzoyl chloride and 3-(3-methoxy-phenyl)-piperidine-3-ol.
Sources & evidence
- ORD record
- ord-e62fabb41a044497b06d7e53c2f50d83
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07790898B2
Reaction notes
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