Dimethyl Sulfoxide → HCID 25056247, compound
Reaction equation
[CH3:1][S:2](=[O:3])[c:4]1[cH:5][c:6](-[n:10]2[n:11][c:12]([CH3:36])[cH:13][c:14]2[NH:15][c:16]2[cH:17][c:18]([NH:23][C:24]([c:25]3[cH:26][c:27]([C:31]([F:32])([F:33])[F:34])[cH:28][cH:29][cH:30]3)=[O:35])[cH:19][cH:20][c:21]2[CH3:22])[n:7][cH:8][n:9]1.[CH3:46][S:47]([CH3:48])=[O:49].[CH3:50][CH:51]([OH:52])[CH3:53].[O:37]1[CH2:38][CH2:39][N:40]([CH2:43][CH2:44][NH2:45])[CH2:41][CH2:42]1>>[c:4]1([NH:45][CH2:44][CH2:43][N:40]2[CH2:39][CH2:38][O:37][CH2:42][CH2:41]2)[cH:5][c:6](-[n:10]2[n:11][c:12]([CH3:36])[cH:13][c:14]2[NH:15][c:16]2[cH:17][c:18]([NH:23][C:24]([c:25]3[cH:26][c:27]([C:31]([F:32])([F:33])[F:34])[cH:28][cH:29][cH:30]3)=[O:35])[cH:19][cH:20][c:21]2[CH3:22])[n:7][cH:8][n:9]1Participants
5
Sources & evidence
- ORD record
- ord-28f20a48377841ac880a2da94f39126a
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (10/10)
Reaction notes
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