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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1820876Erstellt: 25. Oktober 2026

Potassium Carbonate → 1-benzenesulfonyl-3-(3,4-dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/1820876

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt3,4-Dimethoxyphenylboronic acidHCID 2734702—
Edukt3-Bromo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridineHCID 45588134—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-benzenesulfonyl-3-(3,4-dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridineHCID 57891789—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

1-Benzenesulfonyl-3-bromo-1H-pyrrolo[2,3-b]pyridine (4, 1.00 g, 2.96 mmol) was dissolved in tetrahydrofuran (16 mL) and 3,4-dimethoxyphenyl boronic acid (1.35 g, 7.41 mmol), tetrakis(triphenylphosphine)palladium(0) (200 mg, 0.1 mmol), and 1 M potassium carbonate (8 mL) were added. The reaction mixture was heated in a CEM Discover microwave at 120° C. for 10 minutes. The reaction mixture was concentrated under reduced pressure and partitioned between ethyl acetate and water. The organic portions were dried with anhydrous magnesium sulfate, filtered, and the filtrate was adsorbed onto silica. The mixture was purified by flash chromatography (30% ethyl acetate:hexanes) to provide the desired product, 5, (909 mg, 78%). MS(ESI) [M+H+]+=394.9.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07605168B2
Quelldatensatzuspto-grants-2009_10
ORD IDord-cd4a665d843e4f7793eede53cb126882
Quellennotizuspto-grants-2009_10