Pyridinium chloride → 4-p-Hydroxyanilinocarbonylmethylamino-1-(4-phenyl-4-oxobutyl) piperidine
Reaction equation
C[O:2][C:3]1[CH:30]=[CH:29][C:6]([NH:7][C:8]([CH2:10][NH:11][CH:12]2[CH2:17][CH2:16][N:15]([CH2:18][CH2:19][CH2:20][C:21]([C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)=[O:22])[CH2:14][CH2:13]2)=[O:9])=[CH:5][CH:4]=1.Cl.N1C=CC=CC=1>>[OH:2][C:3]1[CH:4]=[CH:5][C:6]([NH:7][C:8]([CH2:10][NH:11][CH:12]2[CH2:13][CH2:14][N:15]([CH2:18][CH2:19][CH2:20][C:21]([C:23]3[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=3)=[O:22])[CH2:16][CH2:17]2)=[O:9])=[CH:29][CH:30]=1Participants
3
Procedure
4-p-Methoxyanilinocarbonylmethylamino-1-(4 -phenyl-4-oxobutyl)-piperidine may be reacted with pyridine hydrochloride to give the title compound.
Sources & evidence
- ORD record
- ord-5d15bf89ac1345128d065d31bf15907e
- Source dataset
- uspto-grants-1977_08
- Patent number
- US04045566
Reaction notes
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