Hydrochloric Acid → 3-[4-(2-methylanilino)piperidin-1-yl]-3-oxo-N-(6-phenyl-3-pyridinyl)propanamide
Reaction equation
[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].[NH:53]1[CH2:54][CH2:55][CH:56]([NH:59][c:60]2[c:61]([CH3:66])[cH:62][cH:63][cH:64][cH:65]2)[CH2:57][CH2:58]1.[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:53]3[CH2:54][CH2:55][CH:56]([NH:59][c:60]4[c:61]([CH3:66])[cH:62][cH:63][cH:64][cH:65]4)[CH2:57][CH2:58]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-1fa491413a0a49c29f362bffd37d2ef9
- Source dataset
- Test data from https://doi.org/10.1039/C8SC04228D
Reaction notes
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