Dimethyl Sulfoxide → HCID 57505480, compound
Reaction equation
[C:35](=[O:36])([O-:37])[O-:38].[C:51]([O:52][CH2:53][CH3:54])(=[O:55])[CH3:56].[CH3:41][S:42](=[O:43])[CH3:44].[Cs+:39].[Cs+:40].[I:1][c:2]1[cH:3][cH:4][c:5]2[n:6]([n:7]1)[cH:8][c:9]([NH:11][C:12](=[O:13])[CH:14]1[CH2:15][CH2:16]1)[n:10]2.[O:46]1[CH2:47][CH2:48][CH2:49][CH2:50]1.[OH2:45].[OH:17][c:18]1[cH:19][cH:20][c:21]([CH3:34])[c:22]([NH:24][C:25](=[O:26])[C:27]2=[N:28][N:29]([CH3:33])[CH2:30][CH:31]2[CH3:32])[cH:23]1>>[c:2]1([O:17][c:18]2[cH:19][cH:20][c:21]([CH3:34])[c:22]([NH:24][C:25](=[O:26])[C:27]3=[N:28][N:29]([CH3:33])[CH2:30][CH:31]3[CH3:32])[cH:23]2)[cH:3][cH:4][c:5]2[n:6]([n:7]1)[cH:8][c:9]([NH:11][C:12](=[O:13])[CH:14]1[CH2:15][CH2:16]1)[n:10]2Participants
9
Sources & evidence
- ORD record
- ord-08aa87336b854a4ca62395073d6142c9
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (7/10)
Reaction notes
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