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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360082Generated: October 26, 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/1360082

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) and 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=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 numberUS07879837B2
Source datasetuspto-grants-2011_02
ORD IDord-f82ca55abb204406a1aeb7efa9215e81
Source noteuspto-grants-2011_02