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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339749Generated: October 29, 2026

Potassium Carbonate → Ethyl 5-(6-methyl-5-{[4-(trifluoromethyl)phenyl]ethynyl}pyrimidin-4-ylaminomethyl)-2-furancarboxylate

https://huagongshe.com/reaction/339749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 5-(chloromethyl)-2-furancarboxylateHCID 263166—
Reactant4-Amino-6-methyl-5-{[4-(trifluoromethyl)phenyl]ethynyl}pyrimidineHCID 68002449—
SolventDimethylformamideHCID 6228—
ProductEthyl 5-(6-methyl-5-{[4-(trifluoromethyl)phenyl]ethynyl}pyrimidin-4-ylaminomethyl)-2-furancarboxylateHCID 44815753—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 4-amino-6-methyl-5-{[4-(trifluoromethyl)phenyl]ethynyl}pyrimidine (2.8 g), ethyl 5-chloromethyl-2-furancarboxylate (1.8 g), potassium carbonate (2.1 g) and N,N-dimethylformamide (120 ml) was heated while stirring at 70° C. for 15 hours. The mixture thus obtained was concentrated under reduced pressure. To the resultant residue, water was added. After extraction was performed with chloroform, an organic phase was dried over anhydrous sodium sulfate and then evaporated. The evaporated residue was purified by column chromatography to obtain a target substance (1 g). The target substance was subjected to e.g., proton nuclear magnetic resonance spectrometry (1H-NMR) and mass spectrometry (MS) and confirmed as the titled compound. Furthermore, MS measurement result is shown.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895565B2
Source datasetuspto-grants-2014_11
ORD IDord-e228e53003564ed7bc00513b74849d0e
Source noteuspto-grants-2014_11