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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 24484생성일: 2026년 10월 24일

Piperidine → 5-acetyl-3-(3-methyl-1H-indol-2-ylmethylene)-1,3-dihydro-indol-2-one

https://huagongshe.com/ko/reaction/24484

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물3-Methyl-1H-indole-2-carbaldehydeHCID 277260—
반응물5-acetyl-2,3-dihydro-1H-indol-2-oneHCID 10219643—
용매EthanolHCID 702—
생성물5-acetyl-3-(3-methyl-1H-indol-2-ylmethylene)-1,3-dihydro-indol-2-oneHCID 5381930375%

반응 단계

A mixture of 5-acetyl-2-oxindole (70 mg), 3-methylindole-2-carbaldehyde (56 mg) (prepared according to Synthetic Communications, 1986, 16, 1799) and piperidine (30 mg) in ethanol (1 mL) was held in a sealed tube at 90° C. overnight. The mixture was cooled to room temperature. The solid was collected by vacuum filtration, washed with cold ethanol and dried in a vacuum to give 83 mg (75% yield) of 5-acetyl-3-(3-methyl-1H-indol-2-ylmethylene)-1,3-dihydro-indol-2-one.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855730B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-0d1f5f5413b047e993118d1e8df8d3b2
출처 메모uspto-grants-2005_02