Dimethyl Sulfoxide → HCID 86597671, compound
Reaction equation
[CH2:50]([N:51]([CH:52]([CH3:53])[CH3:54])[CH:55]([CH3:56])[CH3:57])[CH3:58].[CH3:7][S:8](=[O:9])[CH3:10].[Cl:1][C:2]([C:3]([Cl:4])=[O:5])=[O:6].[Cl:59][CH2:60][Cl:61].[F:11][C:12]([c:13]1[cH:14][c:15]([C:23]([C:24](=[O:25])[N:26]([CH3:27])[c:28]2[cH:29][n:30][c:31]([NH:41][CH2:42][CH:43]([CH3:44])[OH:45])[cH:32][c:33]2-[c:34]2[c:35]([Cl:40])[cH:36][cH:37][cH:38][cH:39]2)([CH3:46])[CH3:47])[cH:16][c:17]([C:19]([F:20])([F:21])[F:22])[cH:18]1)([F:48])[F:49]>>[F:11][C:12]([c:13]1[cH:14][c:15]([C:23]([C:24](=[O:25])[N:26]([CH3:27])[c:28]2[cH:29][n:30][c:31]([NH:41][CH2:42][C:43]([CH3:44])=[O:45])[cH:32][c:33]2-[c:34]2[c:35]([Cl:40])[cH:36][cH:37][cH:38][cH:39]2)([CH3:46])[CH3:47])[cH:16][c:17]([C:19]([F:20])([F:21])[F:22])[cH:18]1)([F:48])[F:49]Participants
6
Sources & evidence
- ORD record
- ord-1a5f343ae671498bb84f624c9129b331
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (3/10)
Reaction notes
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