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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1751110Erstellt: 26. Oktober 2026

Sodium Iodide → (R)-tert-butyl 2-(4-oxo-8-(3-(2-oxoindolin-1-yl)propyl)-1-phenyl-1,3,8-triazaspiro[4.5]decan-3-yl)-2-phenylacetate

https://huagongshe.com/reaction/1751110

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktPotassium CarbonateHCID 11430—
Edukt1-(3-Chloropropyl)-3-methylindolin-2-oneHCID 58046779—
Edukt(R)-tert-butyl 2-(4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decan-3-yl)-2-phenylacetateHCID 66652191—
LösungsmittelMethyl Ethyl KetoneHCID 6569—
Produkt(R)-tert-butyl 2-(4-oxo-8-(3-(2-oxoindolin-1-yl)propyl)-1-phenyl-1,3,8-triazaspiro[4.5]decan-3-yl)-2-phenylacetateHCID 5804677728%

Reaktionsbedingungen

Temperatur81 °C

Reaktionsschritte

A mixture of (R)-tert-butyl 2-(4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decan-3-yl)-2-phenylacetate (250 mg, 0.60 mmol, 1 equiv), 1-(3-chloropropyl)-3-methylindolin-2-one (125.8 mg, 0.60 mmol, 1 equiv), sodium iodide (36 mg, 0.24 mmol, 0.4 equiv), and potassium carbonate (166 mg, 1.2 mmol, 2 equiv) in 2-butanone was stirred at 81° C. for 16 h. After cooling the reaction mixture, the crude mixture was partitioned between ethyl acetate and water. The organic layer was dried over MgSO4, filtered, concentrated, and the crude residue was purified using preparative thin layer chromatography in 10% methanol in dichloromethane to afford the title compound as a cream solid (100 mg, 28%); MS for C36H42N4O4 m/z 595.32 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09156840B2
Quelldatensatzuspto-grants-2015_10
ORD IDord-6f83f9c1c39442cb9b294857931332dd
Quellennotizuspto-grants-2015_10