2-Oxazolidinone, 5,5-dimethyl- → HCID 58484848, compound

HRID 176211Notes

Reaction equation

HRID 176211 reaction equation
[Br:1][c:2]1[cH:3][c:4]([S:24](=[O:25])(=[O:26])[CH3:27])[c:5]([C:8](=[O:9])[N:10]2[CH2:11][CH2:12][N:13]([c:16]3[n:17][cH:18][c:19]([CH3:23])[cH:20][c:21]3[CH3:22])[CH2:14][CH2:15]2)[cH:6][cH:7]1.[CH3:28][C:29]1([CH3:35])[CH2:30][NH:31][C:32](=[O:34])[O:33]1>>[c:2]1([N:31]2[CH2:30][C:29]([CH3:28])([CH3:35])[O:33][C:32]2=[O:34])[cH:3][c:4]([S:24](=[O:25])(=[O:26])[CH3:27])[c:5]([C:8](=[O:9])[N:10]2[CH2:11][CH2:12][N:13]([c:16]3[n:17][cH:18][c:19]([CH3:23])[cH:20][c:21]3[CH3:22])[CH2:14][CH2:15]2)[cH:6][cH:7]1

Participants

3

Reactant 2

HCID 1368922-Oxazolidinone, 5,5-dimethyl-HCID 58484505(4-Bromo-2-methanesulfonylphenyl)[4-(3,5-dimethylpyridin-2-yl)piperazin-1-yl]methanone

Product 1

HCID 58484848HCID 58484848, compound

Sources & evidence

ORD record
ord-c5f5735dcbe043a3a75e8fdac6e92ddb
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)

Reaction notes

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