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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804323Generated: November 1, 2026

(4S)-4-(Benzoyloxymethyl)oxazolidine-2-one → (R)-3-{5-[4-(5-ethyl-3-methylpyridin-2-yl)piperazine-1-carbonyl]pyridin-2-yl}-4-hydroxymethyloxazolidin-2-one

https://huagongshe.com/reaction/1804323

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4S)-4-(Benzoyloxymethyl)oxazolidine-2-oneHCID 16213752—
Reactant(6-Bromopyridin-3-yl)[4-(5-ethyl-3-methylpyridin-2-yl)piperazin-1-yl]methanoneHCID 58484652—
Product(R)-3-{5-[4-(5-ethyl-3-methylpyridin-2-yl)piperazine-1-carbonyl]pyridin-2-yl}-4-hydroxymethyloxazolidin-2-oneHCID 5848477454.4%

Reaction Steps

By reaction and treatment in the same manner as in Example 19 and using (6-bromopyridin-3-yl)[4-(5-ethyl-3-methylpyridin-2-yl)piperazin-1-yl]methanone (530 mg) described in Preparation Example 145 and benzoic acid (R)-2-oxooxazolidin-4-ylmethyl ester (466 mg), the title compound (315 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354401B2
Source datasetuspto-grants-2013_01
ORD IDord-9f72e55245944647934385ee83564fe3
Source noteuspto-grants-2013_01