Dimethyl Sulfate → HCID 178494197, compound
Reaction equation
[CH3:1][CH:2]([c:4]1[n:10][c:8]([OH:9])[c:7]([c:11]2[cH:32][c:16]([O:17][C@@H:18]([c:20]3[c:26]([n:27]4[n:31][cH:30][cH:29][n:28]4)[cH:25][cH:24][c:22]([F:23])[cH:21]3)[CH3:19])[c:14]([NH2:15])[n:13][cH:12]2)[cH:6][cH:5]1)[NH2:3].[CH3:33]OS(OC)(=O)=O>>[CH3:33][O:9][c:8]1[c:7]([c:11]2[cH:32][c:16]([O:17][C@@H:18]([c:20]3[c:26]([n:27]4[n:31][cH:30][cH:29][n:28]4)[cH:25][cH:24][c:22]([F:23])[cH:21]3)[CH3:19])[c:14]([NH2:15])[n:13][cH:12]2)[cH:6][cH:5][c:4]([CH:2]([NH2:3])[CH3:1])[n:10]1Participants
6
Conditions
- Temperature
- 60 °C
Sources & evidence
- ORD record
- ord-2af149b857b945478e9b866a4fedd8e9
- Source dataset
- 39k HTE dataset from Pfizer
- Original link
- View source
Reaction notes
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