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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161586Generated: October 28, 2026

Dimethylformamide → HCID 86617929, compound

https://huagongshe.com/reaction/1161586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(2-Bromoethoxy)tetrahydro-2H-pyranHCID 86621—
ReactantHCID 72312741HCID 72312741—
SolventWaterHCID 962—
ProductHCID 86617929HCID 86617929—

Reaction Steps

To 2 ml of a DMF solution containing 200 mg of [2-(4-cyano-3-fluorophenylimino)-2-(2-fluoro-3-hydroxy-5-methoxyphenyl)-1-methylsulfanylethylidene]carbamic acid methyl ester, 300 mg of potassium carbonate and 0.2 ml of 2-(2-bromoethoxy)tetrahydro-2H-pyran were added. The resulting mixture was stirred at room temperature for 18 hours, and then water was added thereto. The mixture was extracted with ethyl acetate. The organic layer was washed with water and then with 5 saturated brine and dried over anhydrous sodium sulfate. The desiccating agent was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give (2-(4-cyano-3-fluorophenylimino)-2-{2-fluoro-5-methoxy-3-[2-(tetrahydropyran-2-yloxy)ethoxy]phenyl}-1-methylsulfanylethylidene)carbamic acid methyl ester (150 mg) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816522B2
Source datasetuspto-grants-2010_10
ORD IDord-4450c74ef64a43eab6e7da7957325bbd
Source noteuspto-grants-2010_10