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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820892Generated: October 26, 2026

Ethyl Acetate → 4-(3,4-Dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/1820892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant1H-Pyrrolo(2,3-b)pyridineHCID 9222—
Reactant3,4-Dimethoxyphenylboronic acidHCID 2734702—
Reactant4-Chloro-1H-pyrrolo[2,3-b]pyridineHCID 11389493—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventPotassium CarbonateHCID 11430—
Product4-(3,4-Dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridineHCID 11999024—

Reaction Conditions

Temperature150 °C

Reaction Steps

In a microwave reaction tube, 4-chloro-7-azaindole (49, 1.362 g, 8.926 mmol), prepared from 7-azaindole following published procedure (Schneller, S. W.; Luo, Jiann-Kuan. J. Org. Chem. 1980, 45, 4045-4048), 3,4-dimethoxyphenyl boronic acid (4.06 g, 22.3 mmol), and tetrakis(triphenylphosphine)palladium(0) (52 mg, 0.45 mmol) were mixed in 1.0 M potassium carbonate in water (27 mL) and tetrahydrofuran (43 mL). The resulting mixture was heated at 150° C. in a CEM Discover microwave unit for 20 minutes. Ethyl acetate and water were added, and the two layers were separated. The aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with brine and dried over anhydrous sodium sulfate. Concentration under reduced pressure afforded the crude material, which was purified by column chromatography (40-70% ethyl acetate in hexane) to yield the desired product in light yellow solid (50, 974 mg, 3.83 mmol). MS(ESI) [M+H+]+=255.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605168B2
Source datasetuspto-grants-2009_10
ORD IDord-315f66e012a74002863f089961bf69cc
Source noteuspto-grants-2009_10