Pyridine → tert-Butyl 2-cyanopyrrolidine-1-carboxylate
Reaction equation
[C:12](=[O:13])([O:14][C:15]([CH3:16])([CH3:17])[CH3:18])[N:19]1[CH:20]([C:21]([OH:22])=[O:23])[CH2:24][CH2:25][CH2:26]1.[CH3:34][C:35]#[N:36].[CH3:37][CH2:38][O:39][C:40]([CH3:41])=[O:42].[Cl:1][C:2]([C:3]([Cl:4])=[O:5])=[O:6].[NH2-:27].[O:7]=[CH:8][N:9]([CH3:10])[CH3:11].[cH:28]1[cH:29][cH:30][n:31][cH:32][cH:33]1>>[N:9]#[C:21][CH:20]1[N:19]([C:12](=[O:13])[O:14][C:15]([CH3:16])([CH3:17])[CH3:18])[CH2:26][CH2:25][CH2:24]1Participants
8
Sources & evidence
- ORD record
- ord-8d5b667acd49447e89ce7c55185d983e
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (6/10)
Reaction notes
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