Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473954Generated: October 26, 2026

Potassium Carbonate → 5-Methyl-3-(3-trifluoromethyl-phenyl)-imidazo[1,2-a]pyridine-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1473954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTriphenylphosphineHCID 11776—
Reactant3-(Trifluoromethyl)phenylboronic acidHCID 2734388—
ReactantEthyl 3-bromo-5-methylimidazo[1,2-a]pyridine-2-carboxylateHCID 58379339—
CatalystPalladium(2+) acetate--triphenylphosphane (1/2/2)HCID 84538—
Product5-Methyl-3-(3-trifluoromethyl-phenyl)-imidazo[1,2-a]pyridine-2-carboxylic acid ethyl esterHCID 5949614350.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

3-Bromo-5-methyl-imidazo[1,2-a]pyridine-2-carboxylic acid ethyl ester (compound o, 0.6 g, 0.002 mol), potassium carbonate (0.6 g, 0.004 mol), triphenylphosphine (0.06 g, 0.0002 mol), 3-(trifluoromethyl)phenylboronic acid (0.4 g, 0.002 mol) and bis(acetato) bis(triphenylphosphine)palladium (II) (0.08 g, 0.0001 mol) were mixed in a microwave vial. The mixture was purged with argon. Isopropyl alcohol (20 mL) and water (3 mL) was added. The mixture was heated (120° C.) by microwaved for 25 minutes. The solvent removed then water (10 mL) and ethyl acetate (10 mL) was added. The layers were separated and the organic layer dried (magnesium sulfate) then removed. The crude product was chromatographed using 50% ethyl acetate/hexanes to give 350 mg of 5-methyl-3-(3-trifluoromethyl-phenyl)-imidazo[1,2-a]pyridine-2-carboxylic acid ethyl ester as a white solid. Rf 0.42, 50% ethyl acetate/hexanes; MS m/z 349 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018208B2
Source datasetuspto-grants-2015_04
ORD IDord-42e7cf42275145ea8c5c5472de289296
Source noteuspto-grants-2015_04