4-Methoxyphenylacetyl chloride → Hydrochloric Acid
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:13]2[CH:18]=[C:17]([CH2:19][N:20]3[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]3)[CH:16]=[CH:15][N:14]=2)[CH:6]=[C:7]([O:11][CH3:12])[C:8]=1[O:9][CH3:10].[CH3:26][O:27][C:28]1[CH:33]=[CH:32][C:31]([CH2:34][C:35]([Cl:37])=[O:36])=[CH:30][CH:29]=1>>[ClH:37].[CH3:26][O:27][C:28]1[CH:33]=[CH:32][C:31]([CH2:34][C:35]([N:23]2[CH2:24][CH2:25][N:20]([CH2:19][C:17]3[CH:16]=[CH:15][N:14]=[C:13]([C:5]4[CH:6]=[C:7]([O:11][CH3:12])[C:8]([O:9][CH3:10])=[C:3]([O:2][CH3:1])[CH:4]=4)[CH:18]=3)[CH2:21][CH2:22]2)=[O:36])=[CH:30][CH:29]=1.[ClH:37]Participants
4
Procedure
1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-piperazine (103 mg) and (4-methoxyphenyl)acetyl chloride (60 mg) were reacted in the same manner as in Example 46 to obtain the title compound in the form of a hydrochloride.
Sources & evidence
- ORD record
- ord-d11439db855a44f6ac1a2b1127fb3941
- Source dataset
- uspto-grants-2003_04
- Patent number
- US06552188B2
Reaction notes
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