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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227271Generated: October 26, 2026

Potassium Carbonate → HCID 10478188, compound

https://huagongshe.com/reaction/227271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-(2-ethoxyethyl)-3-piperidin-4-yl-1H-indoleHCID 9903600—
ReactantMethyl 5-(bromomethyl)-2-methoxybenzoateHCID 19744340—
SolventMethyl Isobutyl KetoneHCID 7909—
ProductHCID 10478188HCID 10478188112.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 1.9 g (0.0071 mol) of 5-bromomethyl-2-methoxy-benzoic acid methyl ester in 5 ml of methyl isobutylketone was added to a suspension of 1.8 g (0.065 mol) of 1-(2-ethoxyethyl)-3-piperidin-4-yl-1H-indole and 1.8 g (0.013 mol) of potassium carbonate in 45 ml of methyl isobutylketone. The reaction mixture was heated at 60° C. for 20 h. The crude mixture was filtered to remove inorganic salts and the solvent was removed under reduced pressure affording 3.5 g of a crude oil. The crude mixture was purified by flash chromatography over silica gel affording 1.8 g (48% of yield) of 5-{4-[1-(2-ethoxyethyl)-1H-indol-3-yl]-piperidin-1-ylmethy}-2-methoxy-benzoic acid ethyl ester. This ester was dissolved in 18 ml of ethanol and hydrolysed with 2N NaOH at room temperature for 20 hours. The crude mixture was neutralised with 2N HCl aqueous solution and the solvent was removed under reduced pressure. The crude residue was extracted between dichloromethane and water. After drying, filtering and removing the solvent under reduced pressure, the residue obtained was recrystallised with ethanol affording 0.77 g (27% of overall yield) of the expected acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560471B2
Source datasetuspto-grants-2009_07
ORD IDord-a4cd932c0145488dae84ba6a7f0d5d75
Source noteuspto-grants-2009_07