Benzoyl chloride, 3-bromo- → (3-Bromophenyl)-[3-hydroxy-3-(3-methoxyphenyl)-piperidine-1-yl]-methanone
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5](Cl)=[O:6].[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:3]=[C:4]([C:5]([N:21]2[CH2:22][CH2:23][CH2:24][C:19]([OH:25])([C:15]3[CH:16]=[CH:17][CH:18]=[C:13]([O:12][CH3:11])[CH:14]=3)[CH2:20]2)=[O:6])[CH:8]=[CH:9][CH:10]=1Participants
3
Procedure
The compound of Example 21 was prepared according to the general preparation protocol A from 3-bromobenzoyl chloride and 3-(3-methoxy-phenyl)-piperidine-3-ol.
Sources & evidence
- ORD record
- ord-f8a1ac11771f455da58250bbf38cf77a
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07790898B2
Reaction notes
Loading…