Benzoyl chloride, 3,4,5-trimethoxy- → HCID 11560420, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]=[C:10]([O:14][CH3:15])[C:11]=1[O:12][CH3:13])[C:6](Cl)=[O:7].[CH3:16][O:17][C:18]1[CH:19]=[C:20]([C:24]2([OH:30])[CH2:29][CH2:28][CH2:27][NH:26][CH2:25]2)[CH:21]=[CH:22][CH:23]=1>>[OH:30][C:24]1([C:20]2[CH:21]=[CH:22][CH:23]=[C:18]([O:17][CH3:16])[CH:19]=2)[CH2:29][CH2:28][CH2:27][N:26]([C:6]([C:5]2[CH:4]=[C:3]([O:2][CH3:1])[C:11]([O:12][CH3:13])=[C:10]([O:14][CH3:15])[CH:9]=2)=[O:7])[CH2:25]1Participants
3
Procedure
The compound of Example 16 was prepared according to the general preparation protocol A from 3,4,5-trimethoxybenzoyl chloride and 3-(3-methoxy-phenyl)-piperidine-3-ol.
Sources & evidence
- ORD record
- ord-b94fec7527394db59e831dff80a98845
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07790898B2
Reaction notes
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