1,3-Dibromo-5,5-dimethylhydantoin → HCID 178475175, compound
Reaction equation
[Br:40][N:41]1[C:42]([CH3:43])([CH3:44])[C:45](=[O:46])[N:47]([Br:48])[C:49]1=[O:50].[C:1]([CH3:2])(=[O:3])[O:4][CH:5]1[CH2:6][CH:7]([O:36][C:37]([CH3:38])=[O:39])[CH2:8][C:9]2=[CH:10][CH2:11][CH:12]3[CH:13]4[CH2:14][CH2:15][CH:16]([CH:17]([CH2:18][CH2:19][CH2:20][C:21]([CH3:22])([CH3:23])[O:24][C:25]([CH3:26])=[O:27])[CH3:28])[C:29]4([CH3:35])[CH2:30][CH2:31][CH:32]3[C:33]12[CH3:34].[CH2:65]([O:66][C:67](=[O:68])[CH3:69])[CH3:70].[CH3:51][CH2:52][CH2:53][CH2:54][CH2:55][CH3:56].[c:57]1([CH3:58])[c:59]([CH3:60])[cH:61][cH:62][cH:63][cH:64]1>>[C:1]([CH3:2])(=[O:3])[O:4][CH:5]1[CH2:6][CH:7]([O:36][C:37]([CH3:38])=[O:39])[CH2:8][C:9]2=[CH:10][CH:11]=[C:12]3[CH:13]4[CH2:14][CH2:15][CH:16]([CH:17]([CH2:18][CH2:19][CH2:20][C:21]([CH3:22])([CH3:23])[O:24][C:25]([CH3:26])=[O:27])[CH3:28])[C:29]4([CH3:35])[CH2:30][CH2:31][CH:32]3[C:33]12[CH3:34]Participants
6
Sources & evidence
- ORD record
- ord-1ab00078be104f29aecef054a7a2256a
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (4/10)
Reaction notes
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