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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1360089생성일: 2026년 10월 26일

Ethyl Acetate → (S,E)-2-(2,6-dichlorobenzamido)-5-[4-(isopropyl-pyrimidin-2-ylamino)phenyl]pent-4-enoic acid methyl ester

https://huagongshe.com/reaction/1360089

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Potassium CarbonateHCID 11430—
반응물(S)-2-(2,6-dichlorobenzamido)pent-4-enoic acid methyl esterHCID 57762562—
반응물N-(4-iodophenyl)-N-isopropylpyrimidin-2-amineHCID 57762606—
촉매Tri-o-tolylphosphineHCID 80271—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
생성물(S,E)-2-(2,6-dichlorobenzamido)-5-[4-(isopropyl-pyrimidin-2-ylamino)phenyl]pent-4-enoic acid methyl esterHCID 5776256863.3%

반응 조건

온도80 °C

반응 단계

Under an argon atmosphere, palladium acetate (19.9 mg) and tris(2-methylphenyl)phosphine (25.9 mg) were added to a suspension of (S)-2-(2,6-dichlorobenzamido)pent-4-enoic acid methyl ester (514.4 mg), N-(4-iodophenyl)-N-isopropylpyrimidin-2-amine (577.4 mg) and potassium carbonate (352.9 mg) in DMF (6 ml), and the resulting mixture was stirred at 80° C. for 7 hours. After cooling the reaction solution to room temperature, ethyl acetate was added thereto, and the resulting mixture was washed twice with water and once with saturated brine, followed by drying the organic layer 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→1/1→1/3). The obtained crudely purified product was purified again by column chromatography (silica gel, eluent:cyclohexane/ethyl acetate=6/1→4/1→2/1) to obtain (S,E)-2-(2,6-dichlorobenzamido)-5-[4-(isopropyl-pyrimidin-2-ylamino)phenyl]pent-4-enoic acid methyl ester (553.6 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07879837B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-2b4d16a92ed14f61bc7a9dc15cd802dc
출처 메모uspto-grants-2011_02