P-Anisidine → HCID 22557836, compound

HRID 395488Notes

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]=1

Participants

Reactant 2

HCID 7732P-Anisidine

HCID 22558037HCID 22558037, compound

Product 1

HCID 22557836HCID 22557836, compound

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
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06605620B1

Reaction notes

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