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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7082생성일: 2026년 10월 23일

Ethyl Acetate → 4-[2-(tert-Butoxycarbonylamino)ethoxy]-3-methoxy-N-[3-[(E)-2-(3-methylphenyl)vinyl]phenyl]phenylacetamide

https://huagongshe.com/ko/reaction/7082

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물beta-MethylstyreneHCID 12500—
반응물Tri-o-tolylphosphineHCID 80271—
반응물4-[2-(tert-butoxycarbonylamino)ethoxy]-N-(3-iodophenyl)-3-methoxyphenylacetamideHCID 22019609—
촉매Tetrabutylammonium ChlorideHCID 70681—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
생성물4-[2-(tert-Butoxycarbonylamino)ethoxy]-3-methoxy-N-[3-[(E)-2-(3-methylphenyl)vinyl]phenyl]phenylacetamideHCID 22019583152.4%

반응 조건

온도97 °C

반응 단계

Intermediate 4 (1 g) is dissolved in dimethylformamide (10 ml), and thereto are added 3-methylvinylbenzene (826 mg), palladium (II) acetate (105 mg), tris(2-methylphenyl)phosphine (143 mg), tetra-n-butyl ammonium chloride (130 mg), and the mixture is heated with stirring at 97° C. for 18 hours under argon atmosphere. To the reaction solution is added ethyl acetate, and the mixture is washed with water and 2 M hydrochloric acid. The organic layer is dried over sodium sulfate, and the solvent is evaporated under reduced pressure. The residue is purified by silica gel column chromatography (eluent: gradient from 0% to 100% hexane/ethyl acetate) to give 4-[2-(tert-butoxycarbonylamino)-ethoxy]-3-methoxy-N-[3-[(E)-2-(3-methylphenyl)vinyl]phenyl]phenylacetamide (370 mg). This product is treated with 10% hydrogen chloride-methanol to give the desired compound (120 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084176B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-75cc4b5bd19f4a4696cb5248dd41f0c1
출처 메모uspto-grants-2006_08