Chloride → N-benzyl-3-piperidin-1-ylsulfonylbenzamide
Reaction equation
[CH3:9][CH2:10][N:11]([CH2:12][CH3:13])[CH2:14][CH3:15].[CH:43]([Cl:44])([Cl:45])[Cl:46].[Cl-:16].[Cl:17][CH:18]1[N:19]([CH3:20])[CH2:21][CH2:22][NH+:23]1[CH3:24].[Cl:47][CH2:48][Cl:49].[N:25]1([S:31](=[O:32])(=[O:33])[c:34]2[cH:35][c:36]([C:37](=[O:38])[OH:39])[cH:40][cH:41][cH:42]2)[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30]1.[NH2:1][CH2:2][c:3]1[cH:4][cH:5][cH:6][cH:7][cH:8]1>>[NH:1]([CH2:2][c:3]1[cH:4][cH:5][cH:6][cH:7][cH:8]1)[C:37]([c:36]1[cH:35][c:34]([S:31]([N:25]2[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30]2)(=[O:32])=[O:33])[cH:42][cH:41][cH:40]1)=[O:38]Participants
8
Sources & evidence
- ORD record
- ord-0d662ef53d2940f792b670d105a81dbf
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (9/10)
Reaction notes
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