Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804303Generated: October 25, 2026

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

https://huagongshe.com/reaction/1804303

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-4-Methyloxazolidin-2-oneHCID 2734858—
Reactant6-[4-(6-Bromopyridine-3-carbonyl)piperazin-1-yl]-5-methylnicotinonitrileHCID 58484518—
Product(R)-3-{5-[4-(5-cyano-3-methylpyridin-2-yl)piperazine-1-carbonyl]pyridin-2-yl}-4-methyloxazolidin-2-oneHCID 4619027980.8%

Reaction Steps

By reaction and treatment in the same manner as in Example 1 and using 6-[4-(6-bromopyridine-3-carbonyl)piperazin-1-yl]-5-methylnicotinonitrile (200 mg) described in Preparation Example 131 and (R)-4-methyloxazolidin-2-one (79 mg) described in Preparation Example 25, the title compound (170 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354401B2
Source datasetuspto-grants-2013_01
ORD IDord-f12ef8664a8346c18b084e125c29b52e
Source noteuspto-grants-2013_01