2-amino-N-(5-chloropyridin-2-yl)benzamide → HCID 68530566, compound
Reaction equation
[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[N:8]([CH2:9][C:10]([CH2:11][O:12][c:13]1[c:14]([C:15](=[O:16])[OH:17])[cH:18][cH:19][c:20]([C:22]([CH3:23])([CH3:24])[CH3:25])[cH:21]1)([CH3:26])[CH3:27])[CH3:28].[Cl:29][c:30]1[cH:31][cH:32][c:33]([NH:36][C:37]([c:38]2[c:39]([NH2:44])[cH:40][cH:41][cH:42][cH:43]2)=[O:45])[n:34][cH:35]1>>[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[N:8]([CH2:9][C:10]([CH2:11][O:12][c:13]1[c:14]([C:15](=[O:16])[NH:44][c:39]2[c:38]([C:37]([NH:36][c:33]3[cH:32][cH:31][c:30]([Cl:29])[cH:35][n:34]3)=[O:45])[cH:43][cH:42][cH:41][cH:40]2)[cH:18][cH:19][c:20]([C:22]([CH3:23])([CH3:24])[CH3:25])[cH:21]1)([CH3:26])[CH3:27])[CH3:28]Participants
3
Sources & evidence
- ORD record
- ord-9065a32c58724be9858b2005ba0d8599
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (4/10)
Reaction notes
Loading…