Dimethyl Sulfoxide → HCID 67044556, compound
Reaction equation
[C:56](=[O:57])([OH:58])[O-:59].[CH3:11][CH2:12][N:13]([CH2:14][CH3:15])[CH2:16][CH3:17].[CH3:1][S:2]([CH3:3])=[O:4].[CH3:50][CH2:51][O:52][C:53](=[O:54])[CH3:55].[Cl:47][CH2:48][Cl:49].[Cl:5][C:6]([C:7]([Cl:8])=[O:9])=[O:10].[Na+:60].[OH:18][CH:19]([c:20]1[c:21]([C:22]#[N:23])[cH:24][cH:25][cH:26][cH:27]1)[c:28]1[cH:29][c:30]2[cH:31][n:32][n:33]([Si:37]([CH:38]([CH3:39])[CH3:40])([CH:41]([CH3:42])[CH3:43])[CH:44]([CH3:45])[CH3:46])[c:34]2[cH:35][cH:36]1>>[O:18]=[C:19]([c:20]1[c:21]([C:22]#[N:23])[cH:24][cH:25][cH:26][cH:27]1)[c:28]1[cH:29][c:30]2[cH:31][n:32][n:33]([Si:37]([CH:38]([CH3:39])[CH3:40])([CH:41]([CH3:42])[CH3:43])[CH:44]([CH3:45])[CH3:46])[c:34]2[cH:35][cH:36]1Participants
9
Sources & evidence
- ORD record
- ord-aac4cd6141a74ac49ce00a6eb2a8b763
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (4/10)
Reaction notes
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