3-Cyanopyridine → Chloride
Reaction equation
[C:28](#[N:29])[c:30]1[cH:31][n:32][cH:33][cH:34][cH:35]1.[Cl:1][CH2:2][c:3]1[cH:4][cH:5][c:6]([NH:9][C:10](=[O:11])[C:12]2=[CH:13][c:14]3[cH:15][c:16](-[c:22]4[cH:23][cH:24][cH:25][cH:26][cH:27]4)[cH:17][cH:18][c:19]3[CH2:20][CH2:21]2)[cH:7][cH:8]1.[O:36]=[CH:37][N:38]([CH3:39])[CH3:40]>>[CH2:2]([c:3]1[cH:4][cH:5][c:6]([NH:9][C:10](=[O:11])[C:12]2=[CH:13][c:14]3[cH:15][c:16](-[c:22]4[cH:23][cH:24][cH:25][cH:26][cH:27]4)[cH:17][cH:18][c:19]3[CH2:20][CH2:21]2)[cH:7][cH:8]1)[n+:32]1[cH:31][c:30]([C:28]#[N:29])[cH:35][cH:34][cH:33]1.[Cl-:1]Participants
5
Sources & evidence
- ORD record
- ord-a0d13bea442e4f3bb4ac180452f1cc15
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (8/10)
Reaction notes
Loading…