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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2120195생성일: 2026년 10월 26일

Piperidine → 3-(4-Methoxy-3-thiophen-2-yl-benzylidene)-6-pyridin-3-yl-1,3-dihydroindol-2-one

https://huagongshe.com/reaction/2120195

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물6-Pyridin-3-yl-1,3-dihydro-indol-2-oneHCID 21915579—
반응물4-Methoxy-3-(thiophen-2-yl)benzaldehydeHCID 21981024—
용매EthanolHCID 702—
용매Diethyl EtherHCID 3283—
생성물3-(4-Methoxy-3-thiophen-2-yl-benzylidene)-6-pyridin-3-yl-1,3-dihydroindol-2-oneHCID 6988369615%

반응 단계

A mixture of 6-pyridin-3-yl-1,3-dihydro-indol-2-one (100 mg, 0.5 mmol), 4-methoxy-3-thiophen-2-yl-benzaldehyde (110 mg, 0.5 mmol) and piperidine (0.23 mL) in ethanol (4 mL) was heated to reflux and stirred overnight. The reaction mixture was then cooled and diluted with ether to afford a precipitate which removed by filtration. Thefiltrate was column chromatographed (eluant—isopropanol/dichloromethane) to give 30 mg (15%) of 3-(4-methoxy-3-thiophen-2-yl-benzylidene)-6-pyridin-3-yl-1,3-dihydroindol-2-one as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06689806B1
출처 데이터셋uspto-grants-2004_02
ORD IDord-109e72eee4dd4152a9a69a299f59271f
출처 메모uspto-grants-2004_02