Hydrochloric Acid → Methyl 2-(2-aminopropanoylamino)-2-pyridin-2-ylacetate
Reaction equation
[CH3:1][O:2][C:3]([CH:4]([c:5]1[n:6][cH:7][cH:8][cH:9][cH:10]1)[NH:11][C:12]([CH:13]([CH3:14])[NH:15][C:16]([O:17][C:18]([CH3:19])([CH3:20])[CH3:21])=[O:22])=[O:23])=[O:24].[ClH:25].[O:26]1[CH2:27][CH2:28][O:29][CH2:30][CH2:31]1>>[CH3:1][O:2][C:3]([CH:4]([c:5]1[n:6][cH:7][cH:8][cH:9][cH:10]1)[NH:11][C:12]([CH:13]([CH3:14])[NH2:15])=[O:23])=[O:24]Participants
4
Sources & evidence
- ORD record
- ord-6c1c3b744d9c4f3f935cf7f75523f9fd
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (5/10)
Reaction notes
Loading…