4-Phenyloxazolidin-2-one → HCID 77275906, compound

HRID 2316535Notes

Reaction equation

HRID 2316535 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[c:17]([CH3:23])[cH:18][c:19]([CH3:22])[cH:20][cH:21]3)[CH2:14][CH2:15]2)[cH:6][cH:7]1.[c:28]1([CH:34]2[NH:35][C:36](=[O:39])[O:37][CH2:38]2)[cH:29][cH:30][cH:31][cH:32][cH:33]1>>[c:2]1([N:35]2[CH:34]([c:28]3[cH:29][cH:30][cH:31][cH:32][cH:33]3)[CH2:38][O:37][C:36]2=[O:39])[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[c:17]([CH3:23])[cH:18][c:19]([CH3:22])[cH:20][cH:21]3)[CH2:14][CH2:15]2)[cH:6][cH:7]1

Participants

3

Reactant 2

HCID 3497284-Phenyloxazolidin-2-oneHCID 58484856(4-Bromo-2-methanesulfonylphenyl)[4-(2,4-dimethylphenyl)piperazin-1-yl]methanone

Product 1

HCID 77275906HCID 77275906, compound

Sources & evidence

ORD record
ord-0b77b5e088ce413da91e6547cddc6086
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)

Reaction notes

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