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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804301Generated: November 1, 2026

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

https://huagongshe.com/reaction/1804301

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-4-Methyloxazolidin-2-oneHCID 2734858—
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-methyloxazolidin-2-oneHCID 5848467161.9%

Reaction Steps

By reaction and treatment in the same manner as in Example 1 and using (6-bromopyridin-3-yl)[4-(5-ethyl-3-methylpyridin-2-yl)piperazin-1-yl]methanone (1.37 g) described in Preparation Example 115 and (R)-4-methyloxazolidin-2-one (0.53 g) described in Preparation Example 25, the title compound (892 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354401B2
Source datasetuspto-grants-2013_01
ORD IDord-c535e05b827b42278a4d604c4be4ba5b
Source noteuspto-grants-2013_01