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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1815371생성일: 2026년 10월 24일

Piperidine → 3-[4-Methyl-5-(5-methyl-2-oxo-1,2-dihydroindol-3-ylidenemethyl)-1H-pyrrol-3-yl]-propionic acid

https://huagongshe.com/ko/reaction/1815371

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물5-Methylindolin-2-oneHCID 5325716—
반응물3-(5-formyl-4-methyl-1H-pyrrol-3-yl)propanoic acidHCID 15160752—
용매EthanolHCID 702—
생성물3-[4-Methyl-5-(5-methyl-2-oxo-1,2-dihydroindol-3-ylidenemethyl)-1H-pyrrol-3-yl]-propionic acidHCID 5367751742.2%

반응 단계

4-(2-Carboxyethyl)-2-formyl-3-methylpyrrole (90 mg), 74 mg 5-methyl-2-oxindole, and 75 μL piperidine in 2 mL of ethanol were heated at 95° C. for 5 hours. 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 to give 65 mg (42%) 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-afe80207453948e6bd6bd3962f085b59
출처 메모uspto-grants-2005_04