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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1815413생성일: 2026년 10월 24일

6-(3-Ethoxyphenyl)indolin-2-one → 3-{5-[6-(3-Ethoxy-phenyl)-2-oxo-1,2-dihydroindol-3-ylidenemethyl]-4-methyl-1H-pyrrol-3-yl}-propionic acid

https://huagongshe.com/ko/reaction/1815413

반응식

참여 물질

역할이름HCID투입량
반응물6-(3-Ethoxyphenyl)indolin-2-oneHCID 10634636—
반응물3-(5-formyl-4-methyl-1H-pyrrol-3-yl)propanoic acidHCID 15160752—
촉매PiperidineHCID 8082—
용매EthanolHCID 702—
생성물3-{5-[6-(3-Ethoxy-phenyl)-2-oxo-1,2-dihydroindol-3-ylidenemethyl]-4-methyl-1H-pyrrol-3-yl}-propionic acidHCID 5409227096.1%

반응 단계

4-(2-carboxyethyl)-2-formyl-3-methylpyrrole (90.5 mg), 127 mg 6-(3-ethoxyphenyl)-2-oxindole and 2 drops piperidine in 2 mL of ethanol were heated at 90° C. overnight. The reaction mixture was cooled and concentrated. The residue was suspended in 6 N aqueous hydrochloric acid. The precipitate was filtered, washed with water to pH 6 and dried in a vacuum oven overnight to give 200 mg (96%) of the title compound as a brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06878733B1
출처 데이터셋uspto-grants-2005_04
ORD IDord-de31d019a2214d7d92ac1f8c1942f79b
출처 메모uspto-grants-2005_04