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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7083생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/7083

반응식

참여 물질

역할이름HCID투입량
반응물4-[2-(tert-Butoxycarbonylamino)ethoxy]-3-methoxy-N-[3-[(E)-2-(3-methylphenyl)vinyl]phenyl]phenylacetamideHCID 22019583—
촉매PalladiumHCID 23938—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
생성물4-[2-(tert-butoxycarbonylamino)ethoxy]-3-methoxy-N-[3-[2-(3-methylphenyl)ethyl]phenyl]phenylacetamideHCID 2201959779.7%

반응 단계

4-[2-(tert-Butoxycarbonylamino)ethoxy]-3-methoxy-N-[3-[(E)-2-(3-methylphenyl)vinyl]phenyl]phenylacetamide (100 mg) is dissolved in methanol (10 ml) and acetic acid (1 ml), and thereto is added 10% palladium on carbon (10 mg), and the mixture is subjected to catalytic hydrogenation at 50° C. The catalyst is removed by filtration, and the solvent is evaporated to give 4-[2-(tert-butoxycarbonylamino)ethoxy]-3-methoxy-N-[3-[2-(3-methylphenyl)ethyl]phenyl]phenylacetamide (80 mg). This product is treated with 10% hydrogen chloride-methanol to give the desired compound (50 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084176B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-6faf8d70cb6a4ac0804d8ed31f4ed67f
출처 메모uspto-grants-2006_08