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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492177Generated: October 30, 2026

Potassium Carbonate → Methyl 1-(quinolin-4-yl)-1H-indole-3-carboxylate

https://huagongshe.com/reaction/492177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-ChloroquinolineHCID 69140—
ReactantMethyl indole-3-carboxylateHCID 589098—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
ProductMethyl 1-(quinolin-4-yl)-1H-indole-3-carboxylateHCID 68970417152.2%

Reaction Conditions

Temperature20 °C

Reaction Steps

1.73 g (12.5 mmol) of potassium carbonate are added at 20° C. under an argon atmosphere to 0.876 g (5 mmol) of 3-methoxycarbonyl-1H-indole in 10 cm3 of dimethyl sulphoxide. After stirring at 20° C. for 1 hour, 0.654 cm3 (5 mmol) of 4-chloroquinoline is added. After stirring at 100° C. for 43 hours, the reaction mixture is cooled and diluted with 20 cm3 of ethyl acetate and then washed with 3 times 10 cm3 of water and 10 cm3 of saturated aqueous sodium chloride solution. After separating the phases by settling, the organic phase is dried over anhydrous magnesium sulphate, filtered and concentrated to dryness under reduced pressure (2.7 kPa) to give 2.30 g of a residue which is purified by flash chromatography [eluent: cyclohexane/ethyl acetate (7/3 by volume)]. After concentrating the fractions under reduced pressure, 1.07 g of 3-methoxycarbonyl-1-(quinol-4-yl)-1H-indole are obtained in the form of a white solid melting at 142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531663B2
Source datasetuspto-grants-2009_05
ORD IDord-a8185f58f9a4433e87b73dccc1ad12fa
Source noteuspto-grants-2009_05