Hydrochloric Acid → 3-[4-(2-bromo-phenylamino)-piperidin-1-yl]-3-oxo-N-(6-phenyl-pyridin-3-yl)-propionamide
Reaction equation
[Br:53][c:54]1[c:55]([NH:60][CH:61]2[CH2:62][CH2:63][NH:64][CH2:65][CH2:66]2)[cH:56][cH:57][cH:58][cH:59]1.[CH3:39][CH2:40][N:41]=[C:42]=[N:43][CH2:44][CH2:45][CH2:46][N:47]([CH3:48])[CH3:49].[CH:20]([N:21]([CH2:22][CH3:23])[CH:24]([CH3:25])[CH3:26])([CH3:27])[CH3:28].[ClH:50].[ClH:51].[ClH:52].[O:67]=[CH:68][N:69]([CH3:70])[CH3:71].[OH2:72].[OH:29][n:30]1[c:31]2[c:32]([cH:33][cH:34][cH:35][cH:36]2)[n:37][n:38]1.[c:1]1(-[c:7]2[cH:8][cH:9][c:10]([NH:13][C:14]([CH2:15][C:16](=[O:17])[OH:18])=[O:19])[cH:11][n:12]2)[cH:2][cH:3][cH:4][cH:5][cH:6]1>>[c:1]1(-[c:7]2[cH:8][cH:9][c:10]([NH:13][C:14]([CH2:15][C:16](=[O:18])[N:64]3[CH2:63][CH2:62][CH:61]([NH:60][c:55]4[c:54]([Br:53])[cH:59][cH:58][cH:57][cH:56]4)[CH2:66][CH2:65]3)=[O:19])[cH:11][n:12]2)[cH:2][cH:3][cH:4][cH:5][cH:6]1Participants
9
Reactant 8
Product 1
Sources & evidence
- ORD record
- ord-bd88d1ce78b74c26b0c5aba892e54ac1
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (5/10)
Reaction notes
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