4-Chloro-3-nitrobenzoyl chloride → HCID 11646803, compound
Reaction equation
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](Cl)=[O:7])=[CH:4][C:3]=1[N+:11]([O-:13])=[O:12].[CH3:14][O:15][C:16]1[CH:17]=[C:18]([C:22]2([OH:28])[CH2:27][CH2:26][CH2:25][NH:24][CH2:23]2)[CH:19]=[CH:20][CH:21]=1>>[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([N:24]2[CH2:25][CH2:26][CH2:27][C:22]([OH:28])([C:18]3[CH:19]=[CH:20][CH:21]=[C:16]([O:15][CH3:14])[CH:17]=3)[CH2:23]2)=[O:7])=[CH:4][C:3]=1[N+:11]([O-:13])=[O:12]Participants
3
Procedure
The compound of Example 18 was prepared according to the general preparation protocol A from 4-chloro-3-nitrobenzoyl chloride and 3-(3-methoxy-phenyl)-piperidine-3-ol.
Sources & evidence
- ORD record
- ord-2509af333d504bd4800cc8c1accae808
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07790898B2
Reaction notes
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