2-Oxazolidinone, 4-(1-methylethyl)- → HCID 77275999, compound

HRID 1556515

Reaction equation

HRID 1556515 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.[CH:28]([CH3:29])([CH3:30])[CH:31]1[NH:32][C:33](=[O:36])[O:34][CH2:35]1>>[c:2]1([N:32]2[CH:31]([CH:28]([CH3:29])[CH3:30])[CH2:35][O:34][C:33]2=[O:36])[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 5193532-Oxazolidinone, 4-(1-methylethyl)-HCID 58484856(4-Bromo-2-methanesulfonylphenyl)[4-(2,4-dimethylphenyl)piperazin-1-yl]methanone

Product 1

HCID 77275999HCID 77275999, compound

Sources & evidence

ORD record
ord-d2e100c4624e47e7bb8dbeb26a391af3
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (1/10)

Linked notes

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