2-amino-N-(5-chloropyridin-2-yl)benzamide → HCID 44434210, compound
Reaction equation
[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[NH: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].[Cl:28][c:29]1[cH:30][cH:31][c:32]([NH:35][C:36]([c:37]2[c:38]([NH2:43])[cH:39][cH:40][cH:41][cH:42]2)=[O:44])[n:33][cH:34]1>>[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[NH:8][CH2:9][C:10]([CH2:11][O:12][c:13]1[c:14]([C:15](=[O:17])[NH:43][c:38]2[c:37]([C:36]([NH:35][c:32]3[cH:31][cH:30][c:29]([Cl:28])[cH:34][n:33]3)=[O:44])[cH:42][cH:41][cH:40][cH:39]2)[cH:18][cH:19][c:20]([C:22]([CH3:23])([CH3:24])[CH3:25])[cH:21]1)([CH3:26])[CH3:27]Participants
3
Sources & evidence
- ORD record
- ord-ec3c15dcda434aba81b9dfa6b155bf0f
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (1/10)
Reaction notes
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