Hydrochloric Acid → 3-Nitro-1-(2-oxo-2-piperidin-1-ylethyl)pyridin-2-one
Reaction equation
[C:15]([Cl:16])(=[O:17])[C:18]([CH3:19])([CH3:20])[CH3:21].[C:36]([N:37]1[CH2:38][CH2:39][CH2:40][CH2:41][CH2:42]1)(=[O:43])[C:44]([CH3:45])([CH3:46])[CH3:47].[CH2:29]1[CH2:30][CH2:31][NH:32][CH2:33][CH2:34]1.[CH2:48]1[O:49][CH2:50][CH2:51][CH2:52]1.[CH3:22][CH2:23][N:24]([CH2:25][CH3:26])[CH2:27][CH3:28].[ClH:35].[N+:1](=[O:2])([O-:3])[c:4]1[c:5](=[O:14])[n:6]([CH2:10][C:11](=[O:12])[OH:13])[cH:7][cH:8][cH:9]1>>[N+:1](=[O:2])([O-:3])[c:4]1[c:5](=[O:14])[n:6]([CH2:10][C:11](=[O:13])[N:32]2[CH2:31][CH2:30][CH2:29][CH2:34][CH2:33]2)[cH:7][cH:8][cH:9]1Participants
8
Sources & evidence
- ORD record
- ord-c490a6d5631245328f3cab39e757d964
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (6/10)
Reaction notes
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