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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1468014Erstellt: 25. Oktober 2026

5-(Methylsulfonyl)-1H-indole → tert-butyl 4-((6-(5-(methylsulfonyl)-1H-indol-1-yl)pyridin-3-yl)oxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/1468014

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-(Methylsulfonyl)-1H-indoleHCID 14973230—
EduktSodium t-butoxideHCID 23676156—
Edukt4-((6-Chloropyridin-3-yl)oxy)piperidine-1-carboxylateHCID 86696192—
Katalysator2-(2'-Di-tert-butylphosphine)biphenylpalladium(II) acetateHCID 11982262—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkttert-butyl 4-((6-(5-(methylsulfonyl)-1H-indol-1-yl)pyridin-3-yl)oxy)piperidine-1-carboxylateHCID 6780567974,4%

Reaktionsschritte

To a mixture of 4-((6-chloropyridin-3-yl)oxy)piperidine-1-carboxylate (intermediate-6) (0.440 g, 1.4 mmol) and 5-(methylsulfonyl)-1H-indole (intermediate-21) (0.261 g, 1.3 mmol) in anhydrous dioxane (5 mL), 2-(2′-Di-tert-butylphosphine) biphenylpalladium(II)acetate (0.130 g, 0.281 mmol) and NaOtBu (sodium tert.butoxide) (0.312 g, 0.960 mmol) were added. The resultant reaction mixture was refluxed for 4-5 h. The reaction mixture was filtered over celite and filtrate was concentrated in vacuo. The residue was purified by flash column chromatography to give tert-butyl 4-((6-(5-(methylsulfonyl)-1H-indol-1-yl)pyridin-3-yl)oxy)piperidine-1-carboxylate (0.337 g, 50%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09000175B2
Quelldatensatzuspto-grants-2015_04
ORD IDord-f3480cbd231c4f45a147bb0ac3d2f12e
Quellennotizuspto-grants-2015_04