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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804266Generated: October 27, 2026

(R)-4-Methyloxazolidin-2-one → (R)-3-{4-[4-(3-chloro-5-methylpyridin-2-yl)piperazine-1-carbonyl]-3-fluorophenyl}-4-methyloxazolidin-2-one

https://huagongshe.com/reaction/1804266

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-4-Methyloxazolidin-2-oneHCID 2734858—
Reactant(4-Bromo-2-fluorophenyl)[4-(3-chloro-5-methylpyridin-2-yl)piperazin-1-yl]methanoneHCID 58484756—
Product(R)-3-{4-[4-(3-chloro-5-methylpyridin-2-yl)piperazine-1-carbonyl]-3-fluorophenyl}-4-methyloxazolidin-2-oneHCID 5848481395.5%

Reaction Steps

By reaction and treatment in the same manner as in Example 1 and using (4-bromo-2-fluorophenyl)[4-(3-chloro-5-methylpyridin-2-yl)piperazin-1-yl]methanone (626 mg) described in Preparation Example 110 and (R)-4-methyloxazolidin-2-one (227 mg) described in Preparation Example 25, the title compound (627 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354401B2
Source datasetuspto-grants-2013_01
ORD IDord-0d443581bab64945a7ede42ab14f1b3a
Source noteuspto-grants-2013_01