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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804342Generated: October 25, 2026

(S)-5-methyloxazolidin-2-one → (S)-5-methyl-3-{4-[4-(3,5,6-trimethylpyridin-2-yl)piperazine-1-carbonyl]phenyl}oxazolidin-2-one

https://huagongshe.com/reaction/1804342

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-5-methyloxazolidin-2-oneHCID 21794663—
Reactant(4-Iodophenyl)[4-(3,5,6-trimethylpyridin-2-yl)piperazin-1-yl]methanoneHCID 58484793—
Product(S)-5-methyl-3-{4-[4-(3,5,6-trimethylpyridin-2-yl)piperazine-1-carbonyl]phenyl}oxazolidin-2-oneHCID 5848450175.5%

Reaction Steps

By reaction and treatment in the same manner as in Example 149 and using (4-iodophenyl)[4-(3,5,6-trimethylpyridin-2-yl)piperazin-1-yl]methanone (435 mg) described in Preparation Example 176 and (S)-5-methyloxazolidin-2-one (121 mg) described in Preparation Example 42, the title compound (308 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354401B2
Source datasetuspto-grants-2013_01
ORD IDord-f55d5c79ec4a425faf3aad5c6b0cf283
Source noteuspto-grants-2013_01