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HRID 1869154생성일: 2026년 10월 26일

Potassium Carbonate → 3-methoxycarbonyl-1-(2-(trifluoromethyl)quinol-4-yl)-1H-indole

https://huagongshe.com/reaction/1869154

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Methyl indole-3-carboxylateHCID 589098—
반응물4-Chloro-2-(trifluoromethyl)quinolineHCID 2736709—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물3-methoxycarbonyl-1-(2-(trifluoromethyl)quinol-4-yl)-1H-indoleHCID 6897059254%

반응 조건

온도100 °C

반응 단계

1.04 g (7.5 mmol) of potassium carbonate and 0.695 g (3 mmol) of 4-chloro-2-(trifluoromethyl)quinoline are added to 0.526 g (3 mmol) of 3-methoxycarbonyl-1H-indole in 10 cm3 of dimethylformamide under an argon atmosphere. After stirring at a temperature in the region of 100° C. for 20 hours, the reaction mixture is cooled and diluted with 100 cm3 of ethyl acetate and 100 cm3 of water. The organic phase is separated off by settling and washed with twice 100 cm3 of water and 100 cm3 of saturated aqueous sodium chloride solution and then it is dried over magnesium sulphate, filtered and concentrated to dryness under reduced pressure (2.7 kPa), resulting in an orange-coloured oil. This oil is triturated in 20 cm3 of isopropyl ether and the resulting precipitate is filtered off, giving 0.6 g of 3-methoxycarbonyl-1-(2-(trifluoromethyl)quinol-4-yl)-1H-indole in the form of a yellow powder. Mass spectrum (EI): m/e 370 (M+•), m/e 339.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07638521B2
출처 데이터셋uspto-grants-2009_12
ORD IDord-69445a605d934814a3a5766549698cb2
출처 메모uspto-grants-2009_12