4-Aminophenol → 4-(3,5-Dichloro-pyridin-4-yloxy)-phenylamine
Reaction equation
[CH3:29][CH2:30][O:31][C:32](=[O:33])[CH3:34].[CH3:9][C:10]([CH3:11])([O-:12])[CH3:13].[Cl:15][c:16]1[cH:17][n:18][cH:19][c:20]([Cl:23])[c:21]1[Cl:22].[K+:14].[NH2:1][c:2]1[cH:3][cH:4][c:5]([OH:6])[cH:7][cH:8]1.[O:24]=[CH:25][N:26]([CH3:27])[CH3:28]>>[NH2:1][c:2]1[cH:3][cH:4][c:5]([O:6][c:21]2[c:16]([Cl:15])[cH:17][n:18][cH:19][c:20]2[Cl:23])[cH:7][cH:8]1Participants
7
Sources & evidence
- ORD record
- ord-e559afb62105453e898827662a914822
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (6/10)
Reaction notes
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