Dimethyl Sulfoxide → HCID 19435012, compound
Reaction equation
[Br:1][c:2]1[c:3]([F:35])[c:4]2[c:5]([c:6](=[O:24])[cH:7][c:8](-[c:10]3[cH:11][c:12]([F:23])[c:13]([NH:16][C:17]([C:18]([CH3:19])([CH3:20])[CH3:21])=[O:22])[cH:14][cH:15]3)[o:9]2)[c:25]([NH:28][C:29]([C:30]([CH3:31])([CH3:32])[CH3:33])=[O:34])[c:26]1[F:27].[CH3:36][N:37]1[CH2:38][CH2:39][NH:40][CH2:41][CH2:42]1.[CH3:44][S:45](=[O:46])[CH3:47].[OH2:43]>>[c:2]1([N:40]2[CH2:39][CH2:38][N:37]([CH3:36])[CH2:42][CH2:41]2)[c:3]([F:35])[c:4]2[c:5]([c:6](=[O:24])[cH:7][c:8](-[c:10]3[cH:11][c:12]([F:23])[c:13]([NH:16][C:17]([C:18]([CH3:19])([CH3:20])[CH3:21])=[O:22])[cH:14][cH:15]3)[o:9]2)[c:25]([NH:28][C:29]([C:30]([CH3:31])([CH3:32])[CH3:33])=[O:34])[c:26]1[F:27]Participants
5
Sources & evidence
- ORD record
- ord-ede1ec40d42445328cb0a38c9d4cdca4
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (9/10)
Reaction notes
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