alpha-Phenyl-2-piperidino-benzylamine → Methyl 3-methoxy-4-[N-(alpha-phenyl-2-piperidino-benzyl)-aminocarbonylmethyl]-benzoate
Reaction equation
[C:1]1([CH:7]([NH2:20])[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[N:14]2[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:21][O:22][C:23]1[CH:28]=[C:27]([C:29]([O:31][CH3:32])=[O:30])[CH:26]=[CH:25][C:24]=1[CH2:33][C:34](O)=[O:35]>>[CH3:21][O:22][C:23]1[CH:28]=[C:27]([CH:26]=[CH:25][C:24]=1[CH2:33][C:34]([NH:20][CH:7]([C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[N:14]1[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1)=[O:35])[C:29]([O:31][CH3:32])=[O:30]Participants
3
Procedure
Prepared from α-phenyl-2-piperidino-benzylamine and 2-methoxy-4-methoxycarbonyl-phenylacetic acid.
Sources & evidence
- ORD record
- ord-8192120f34b549539d06530dd9af28a3
- Source dataset
- uspto-grants-1993_06
- Patent number
- US05216167
Reaction notes
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