tert-butyl 4-(4-methoxyanilino)tetrahydro-1(2H)-pyridinecarboxylate → 1-(tert-butoxycarbonyl)-4-[N-(4-methoxyphenyl)-N-[[2-(3,4-dimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine
Reaction equation
[CH3:1][O:2][c:3]1[cH:4][cH:5][c:6]([NH:9][CH:10]2[CH2:11][CH2:12][N:13]([C:16](=[O:17])[O:18][C:19]([CH3:20])([CH3:21])[CH3:22])[CH2:14][CH2:15]2)[cH:7][cH:8]1.[Cl:23][CH2:24][c:25]1[cH:26][c:27](-[c:31]2[cH:32][c:33]([O:39][CH3:40])[c:34]([O:37][CH3:38])[cH:35][cH:36]2)[n:28][cH:29][cH:30]1>>[CH3:1][O:2][c:3]1[cH:4][cH:5][c:6]([N:9]([CH:10]2[CH2:11][CH2:12][N:13]([C:16](=[O:17])[O:18][C:19]([CH3:20])([CH3:21])[CH3:22])[CH2:14][CH2:15]2)[CH2:24][c:25]2[cH:26][c:27](-[c:31]3[cH:32][c:33]([O:39][CH3:40])[c:34]([O:37][CH3:38])[cH:35][cH:36]3)[n:28][cH:29][cH:30]2)[cH:7][cH:8]1Participants
3
Sources & evidence
- ORD record
- ord-3ce1f2d1d797473ab3ca262d0ddae40f
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (2/10)
Reaction notes
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