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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49122생성일: 2026년 10월 24일

Ethanol → 6-Pyridin-3-yl-1,3-dihydro-indol-2-one

https://huagongshe.com/ko/reaction/49122

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Sodium CarbonateHCID 10340—
반응물6-bromo-2,3-dihydro-1H-indol-2-oneHCID 2773289—
반응물Pyridine-3-boronic acid propane diolHCID 69587225—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물6-Pyridin-3-yl-1,3-dihydro-indol-2-oneHCID 2191557942%

반응 조건

온도100 °C

반응 단계

To a solution of 6-bromo-2-oxindole (4 g, 26.3 mmol) dissolved in 60 mL of toluene and 60 mL of ethanol with stirring and a little heating tetrakis(triphenyl-phosphine)palladium(0) (2.3 g, 1.9 mmol) was added followed by a 2M aqueous solution of sodium carbonate (50 mL, 100 mmol) and pyridine-3-boronic acid propane diol (5 g, 30.7 mmol). The mixture was heated in a 100° C. oil bath for 12 hours. The cooled reaction was diluted with ethyl acetate (500 mL), washed with saturated aqueous sodium bicarbonate (200 mL), water (200 mL) and brine (200 mL). The organic layer was dried with magnesium sulfate and concentrated to afford a brown solid. The residue was triturated with methylene chloride/diethyl ether to give 2.32 g (42%) of 6-pyridin-3-yl-1,3-dihydro-indol-2-one as a brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706709B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-c51a563b1d5e48e99b901ce71d587a2a
출처 메모uspto-grants-2004_03