돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 24477생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/24477

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물3-Methyl-1H-indole-2-carbaldehydeHCID 277260—
반응물5-Methylindolin-2-oneHCID 5325716—
용매EthanolHCID 702—
생성물5-methyl-3-(3-methyl-1H-indol-2-ylmethylene)-1,3-dihydroindol-2-oneHCID 5375537874%

반응 단계

A mixture of 5-methyl-2-oxindole (59 mg), 3-methylindole-2-carbaldehyde (56 mg) 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 oven to give 72 mg (74%) of 5-methyl-3-(3-methyl-1H-indol-2-ylmethylene)-1,3-dihydroindol-2-one.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855730B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-6971769eafbc44aa928743994cee0fcd
출처 메모uspto-grants-2005_02