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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230367Generated: October 25, 2026

2-(4-Iodophenoxy)pyrimidine → 2-(2,6-Dichlorobenzamido)-5-[4-(pyrimidin-2-yloxy)phenyl]pent-4-ynoic acid methyl ester

https://huagongshe.com/reaction/230367

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Iodophenoxy)pyrimidineHCID 1484617—
Reactant2-(2,6-Dichlorobenzamido)pent-4-ynoic acid methyl esterHCID 20610296—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventTHF diisopropylamineHCID 18968793—
Product2-(2,6-Dichlorobenzamido)-5-[4-(pyrimidin-2-yloxy)phenyl]pent-4-ynoic acid methyl esterHCID 5776247786.2%

Reaction Steps

Under an argon atmosphere, copper iodide (2.8 mg) and dichlorobis(triphenylphosphine)palladium (5.2 mg) were added to a solution of 2-(2,6-dichlorobenzamido)pent-4-ynoic acid methyl ester (74 mg), 2-(4-iodophenoxy)pyrimidine (81 mg) in THF/diisopropylamine (3/1) mixture (5 ml), and the resulting mixture was stirred at room temperature for 2 hours. The reaction solution was concentrated and ethyl acetate was added to the residue. The insoluble matter was removed by filtration, and the filtrate was washed once with water and once with saturated brine and dried over anhydrous sodium sulfate. After removing anhydrous sodium sulfate by filtration, the filtrate was concentrated. The residue was purified by column chromatography (silica gel, eluent: cyclohexane/chloroform 10=2/1-cyclohexane/chloroform=1/3) to obtain 2-(2,6-dichlorobenzamido)-5-[4-(pyrimidin-2-yloxy)phenyl]pent-4-ynoic acid methyl ester (100 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566724B2
Source datasetuspto-grants-2009_07
ORD IDord-1356b306c5a748a58c42535df6be0692
Source noteuspto-grants-2009_07