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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804250Generated: October 25, 2026

(S)-5-methyloxazolidin-2-one → (S)-3-{4-[4-(5-cyclopropyl-3-methylpyridin-2-yl)piperazine-1-carbonyl]phenyl}-5-methyloxazolidin-2-one

https://huagongshe.com/reaction/1804250

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-5-methyloxazolidin-2-oneHCID 21794663—
Reactant[4-(5-Cyclopropyl-3-methylpyridin-2-yl)piperazin-1-yl](4-iodophenyl)methanoneHCID 58484841—
Product(S)-3-{4-[4-(5-cyclopropyl-3-methylpyridin-2-yl)piperazine-1-carbonyl]phenyl}-5-methyloxazolidin-2-oneHCID 6738087981.9%

Reaction Steps

By reaction and treatment in the same manner as in Example 149 and using [4-(5-cyclopropyl-3-methylpyridin-2-yl)piperazin-1-yl](4-iodophenyl)methanone (447 mg) described in Preparation Example 97 and (S)-5-methyloxazolidin-2-one (121 mg) described in Preparation Example 42, the title compound (344 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354401B2
Source datasetuspto-grants-2013_01
ORD IDord-95232b88e6334e979ca3ad11af4b29ff
Source noteuspto-grants-2013_01