P-Anisidine → HCID 22557836, compound
Reaction equation
[Cl:1][C:2]1[C:7]([O:8][CH3:9])=[CH:6][C:5]([C:10]2[CH:15]=[C:14]([CH2:16][N:17]3[CH2:22][CH2:21][C:20](=O)[CH2:19][CH2:18]3)[CH:13]=[CH:12][N:11]=2)=[CH:4][C:3]=1[O:24][CH3:25].[CH3:26][O:27][C:28]1[CH:33]=[CH:32][C:31]([NH2:34])=[CH:30][CH:29]=1>>[CH3:26][O:27][C:28]1[CH:33]=[CH:32][C:31]([NH:34][CH:20]2[CH2:21][CH2:22][N:17]([CH2:16][C:14]3[CH:13]=[CH:12][N:11]=[C:10]([C:5]4[CH:4]=[C:3]([O:24][CH3:25])[C:2]([Cl:1])=[C:7]([O:8][CH3:9])[CH:6]=4)[CH:15]=3)[CH2:18][CH2:19]2)=[CH:30][CH:29]=1Participants
3
Procedure
1-[[2-(4-Chloro-3,5-dimethoxyphenyl)pyridin-4-yl]methyl]-4-piperidone (690 mg) and p-anisidine (283 mg) were reacted in the same manner as described in Preparation Example 37 to give the title compound.
Workup
- customas described in Preparation Example 37
Sources & evidence
- ORD record
- ord-ff366d60530c4a4e8e8b332e3206af3a
- Source dataset
- uspto-grants-2003_08