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HRID 1814113Erstellt: 24. Oktober 2026

Water → 6-(1-Benzenesulfonyl-5-methylthio-1h-pyrrolo[2,3-b]pyridin-2-yl)nicotinic acid ethyl ester

https://huagongshe.com/de/reaction/1814113

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPotassium AcetateHCID 517044—
Edukt2-Benzenesulfonylamino-3-iodo-5-methylthiopyridineHCID 15486851—
Edukt5-Ethoxycarbonyl-2-trimethylsilylethynylpyridineHCID 22504397—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt6-(1-Benzenesulfonyl-5-methylthio-1h-pyrrolo[2,3-b]pyridin-2-yl)nicotinic acid ethyl esterHCID 6844473998,5%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of 2-benzenesulfonylamino-5-methylthio-3-iodo-pyridine (100 mg) in 1,4-dioxane (2.5 ml), 5-ethoxycarbonyl-2-trimethylsilylethynylpyridine (185 mg), bistriphenylphosphine palladium dichloride (9 mg), cuprous iodide (5 mg) and potassium acetate (37 mg) were added successively and the mixture was stirred in a sealed tube at 100° C. for 15 hours. After cooling, the reaction solution was poured into water, extracted with ethyl acetate, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was separated using silica gel preparative thin-layer chromatography (hexane:ethyl acetate=2:1) to obtain 110 mg of the desired product as an orange oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06875770B2
Quelldatensatzuspto-grants-2005_04
ORD IDord-0f1fd7e7c0f54fbc91234c3ff00dc5b1
Quellennotizuspto-grants-2005_04