Hydrochloric Acid → N-biphenyl-4-yl-3-[4-(2-tert-butyl-phenylamino)-piperidin-1-yl]-3-oxo-propionamide
Reaction equation
[C:53]([CH3:54])([CH3:55])([CH3:56])[c:57]1[c:58]([NH:63][CH:64]2[CH2:65][CH2:66][NH:67][CH2:68][CH2:69]2)[cH:59][cH:60][cH:61][cH:62]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:70]=[CH:71][N:72]([CH3:73])[CH3:74].[OH2:75].[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:14]2[cH:15][cH:16][cH:17][cH:18][cH:19]2)[cH:2][cH:3][c:4]([NH:7][C:8]([CH2:9][C:10](=[O:11])[OH:12])=[O:13])[cH:5][cH:6]1>>[c:1]1(-[c:14]2[cH:15][cH:16][cH:17][cH:18][cH:19]2)[cH:2][cH:3][c:4]([NH:7][C:8]([CH2:9][C:10](=[O:12])[N:67]2[CH2:66][CH2:65][CH:64]([NH:63][c:58]3[c:57]([C:53]([CH3:54])([CH3:55])[CH3:56])[cH:62][cH:61][cH:60][cH:59]3)[CH2:69][CH2:68]2)=[O:13])[cH:5][cH:6]1Participants
9
Reactant 8
Product 1
Sources & evidence
- ORD record
- ord-afbc09b714794ed28b535f1d31a7e29b
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (7/10)
Reaction notes
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