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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869162Generated: October 26, 2026

Potassium Carbonate → 3-methoxycarbonyl-1-(7-(trifluoromethyl)quinol-4-yl)-1H-indole

https://huagongshe.com/reaction/1869162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-7-(trifluoromethyl)quinolineHCID 67668—
ReactantMethyl indole-3-carboxylateHCID 589098—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product3-methoxycarbonyl-1-(7-(trifluoromethyl)quinol-4-yl)-1H-indoleHCID 6897059486.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

1.04 g (7.5 mmol) of potassium carbonate and 0.695 g (3 mmol) of 4-chloro-7-(trifluoromethyl)quinoline are added to 0.525 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 0.96 g of 3-methoxycarbonyl-1-(7-(trifluoromethyl)quinol-4-yl)-1H-indole in the form of a yellow powder. Mass spectrum (EI): m/e 370 (M+•), m/e 339.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07638521B2
Source datasetuspto-grants-2009_12
ORD IDord-c58b1b237713470ba35e5fb384018159
Source noteuspto-grants-2009_12