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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 24505생성일: 2026년 10월 26일

Acetic Acid → 3-[2-(5-methyl-2-oxo-1,2-dihydroindol-3-ylidenemethyl)-4,5,6,7-tetrahydro-1H-indol-3-yl]-propionic acid

https://huagongshe.com/reaction/24505

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물PiperidineHCID 8082—
반응물5-Methylindolin-2-oneHCID 5325716—
반응물3-(2-formyl-4,5,6,7-tetrahydro-1H-indol-3-yl)propionic acidHCID 10609002—
용매EthanolHCID 702—
생성물3-[2-(5-methyl-2-oxo-1,2-dihydroindol-3-ylidenemethyl)-4,5,6,7-tetrahydro-1H-indol-3-yl]-propionic acidHCID 6976469281.4%

반응 단계

A mixture of 3-(2-formyl-4,5,6,7-tetrahydro-1H-indol-3-yl)-propionic acid (5.4 g), 3.2 g of 5-methyl-2-oxindole and 2.7 g of piperidine in 25 mL of ethanol was refluxed for 4 hours. Upon addition of acetic acid (8 mL), a precipitate formed. The mixture was refluxed for 5 minutes and cooled to ambient temperature. The precipitate was collected by vacuum filtration and washed with 20 mL of ethanol. The solids were slurry-washed with 30 mL of refluxing ethanol, cooled, collected by vacuum filtration, washed with 30 mL of ethanol and vacuum dried to give 6.2 g (80% yield) of 3-[2-(5-methyl-2-oxo-1,2-dihydroindol-3-ylidenemethyl)-4,5,6,7-tetrahydro-1H-indol-3-yl]-propionic acid as an orange solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855730B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-a3cc19c140974049b06cace0ee2b617a
출처 메모uspto-grants-2005_02