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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844507Generated: November 1, 2026

2-(Pyridin-4-yl)malonaldehyde → (S)-N-((3-(3-fluoro-4-(4-(pyridin-4-yl)-1H-pyrazol-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide

https://huagongshe.com/reaction/1844507

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Pyridin-4-yl)malonaldehydeHCID 2737246—
Reactant(S)-N-((3-(3-fluoro-4-hydrazinophenyl)-2-oxooxazolidin-5-yl)methyl)acetamideHCID 10731576—
SolventEthanolHCID 702—
Product(S)-N-((3-(3-fluoro-4-(4-(pyridin-4-yl)-1H-pyrazol-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamideHCID 7147748066.3%

Reaction Steps

100 mg (0.354 mmol) of (S)—N-{[3-(3-fluoro-4-hydrazinophenyl)-2-oxooxazolidin-5-yl]methyl}-acetamide and 52.8 mg (0.354 mmol) of 2-(4-pyridyl)malondialdehyde were combined with 5 mL ethanol as a solvent. Then, the resultant mixture was slowly heated to reflux, thereby the solid was substantially dissolved. TLC monitoring was performed to determine completion of the reaction. Then, the resultant mixture was cooled to room temperature and vacuum filtered to afford the product (13a) as a light yellow solid, with a yield of 66.3%, melting point: 203.8-205.0° C., HPLC: 99.97%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946436B2
Source datasetuspto-grants-2015_02
ORD IDord-e84dd3d7177f4e37a0b4eaa0b82da4ba
Source noteuspto-grants-2015_02