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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1838354Erstellt: 27. Oktober 2026

1,4-Dioxane → 1-Benzenesulfonyl-5-methanesulfonyl-2-(3-pyridyl)indole

https://huagongshe.com/reaction/1838354

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,4-DioxaneHCID 31275—
EduktPotassium AcetateHCID 517044—
Edukt3-(Trimethylsilylethynyl)pyridineHCID 4100857—
Edukt1-Benzenesulfonylamino-2-iodo-4-methanesulfonylbenzeneHCID 22504376—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-Benzenesulfonyl-5-methanesulfonyl-2-(3-pyridyl)indoleHCID 2250441463%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 3-trimethylsilylethynylpyridine (1.07 g), 2-benzenesulfonylamino-3-iodo-5-methanesulfonylbenzene (1.75 g), potassium acetate (1.60 g), cuprous iodide (60 mg), dichlorobis(triphenylphosphine)palladium (0.20 g) and 1,4-dioxane (4 ml) was stirred at 100° C. for 12 hours under nitrogen atmosphere. To the reaction solution were added water and ethyl acetate. The insolubles were filtered off. The filtrate was extracted with ethyl acetate, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography (hexane:ethyl acetate=1:3) to obtain 1.04 g of the desired product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06673797B1
Quelldatensatzuspto-grants-2004_01
ORD IDord-7a7a002b8c85481c9a4eb708b7aa9288
Quellennotizuspto-grants-2004_01