Dimethyl Sulfoxide → HCID 178481334, compound
Reaction equation
[C:42]([O-:43])(=[O:44])[O-:45].[CH3:1][S:2](=[O:3])[CH3:4].[Cl:5][c:6]1[c:7]([CH2:8][n:9]2[c:10]([N:24]3[CH2:25][CH:26]([NH:30][C:31]([O:32][C:33]([CH3:34])([CH3:35])[CH3:36])=[O:37])[CH2:27][CH2:28][CH2:29]3)[c:11]([C:22]#[N:23])[c:12]3[n:13]([CH3:21])[c:14](=[O:20])[n:15]([CH3:19])[c:16](=[O:18])[c:17]23)[cH:38][cH:39][cH:40][cH:41]1.[K+:46].[K+:47].[OH2:50].[OH:48][OH:49]>>[Cl:5][c:6]1[c:7]([CH2:8][n:9]2[c:10]([N:24]3[CH2:25][CH:26]([NH:30][C:31]([O:32][C:33]([CH3:34])([CH3:35])[CH3:36])=[O:37])[CH2:27][CH2:28][CH2:29]3)[c:11]([C:22]([NH2:23])=[O:43])[c:12]3[n:13]([CH3:21])[c:14](=[O:20])[n:15]([CH3:19])[c:16](=[O:18])[c:17]23)[cH:38][cH:39][cH:40][cH:41]1Participants
7
Sources & evidence
- ORD record
- ord-11525cf63a314983bf34c758c7634335
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (5/10)
Reaction notes
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