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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820896Generated: October 26, 2026

4-(Methanesulfonyl)phenylboronic acid → (2-Ethoxy-naphthalen-1-yl)-[3-(4-methanesulfonyl-phenyl)-pyrrolo[2,3-b]pyridin-1-yl]-methanone

https://huagongshe.com/reaction/1820896

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Methanesulfonyl)phenylboronic acidHCID 2734364—
Reactant3-Bromo-1-(2-ethoxy naphthoyl)-7-azaindoleHCID 49758913—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
SolventPotassium CarbonateHCID 11430—
Product(2-Ethoxy-naphthalen-1-yl)-[3-(4-methanesulfonyl-phenyl)-pyrrolo[2,3-b]pyridin-1-yl]-methanoneHCID 57891760—

Reaction Conditions

Temperature60 °C

Reaction Steps

(3-Bromo-pyrrolo[2,3-b]pyridin-1-yl)-(2-ethoxy-naphthalen-1-yl)-methanone 85 (35 mg, 0.0088 mmol), 4-Methanesulfonyl-phenylboronic acid (35 mg, 0.18 mmol) and tetrakis(triphenylphosphine)palladium(0) (5 mg) were stirred in tetrahydrofuran (16 mL) and potassium carbonate solution (8.0 mL, 1 M aqueous). The reaction mixture was stirred over night at 60° C. The reaction mixture was concentrated under reduced pressure and partitioned between ethyl acetate and brine. The organic portion was dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated and purified by flash chromatography (ethyl acetate:hexanes 20%-100%). The desired product, 84 was obtained as a pale yellow powder (10 mg, 20%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605168B2
Source datasetuspto-grants-2009_10
ORD IDord-49eebb93aa4f4d25af5bc8db85a5d876
Source noteuspto-grants-2009_10