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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1365704생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1365704

반응식

참여 물질

역할이름HCID투입량
반응물2-(4-Iodophenoxy)pyrimidineHCID 1484617—
반응물2-(2,6-Dichlorobenzamido)pent-4-ynoic acid methyl esterHCID 20610296—
촉매Copper iodideHCID 83717—
촉매HCID 178418476HCID 178418476—
용매THF diisopropylamineHCID 18968793—
생성물2-(2,6-Dichlorobenzamido)-5-[4-(pyrimidin-2-yloxy)phenyl]pent-4-ynoic acid methyl esterHCID 5776247786.2%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07893046B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-1caf893053774d72ab85307ca4d40676
출처 메모uspto-grants-2011_02