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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1814102Erstellt: 26. Oktober 2026

Ethanol → 1-(4-Fluorobenzyl)-5-methanesulfonyl-2-(5-methyl-[1,2,4]oxadiazol-3-yl)indole

https://huagongshe.com/reaction/1814102

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktPotassium HydroxideHCID 14797—
EduktHydroxyamine hydrochlorideHCID 443297—
Edukt2-Cyano-1-(4-fluorobenzyl)-5-methanesulfonylindoleHCID 22504448—
Produkt1-(4-Fluorobenzyl)-5-methanesulfonyl-2-(5-methyl-[1,2,4]oxadiazol-3-yl)indoleHCID 22504406—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of the compound obtained in Example 24 (1) (68 mg), hydroxylamine hydrochloride (22 mg), potassium hydroxide (18 mg) and ethanol (1 ml) was heated under reflux for 2 hours. After the insolubles were filtered off, the reaction mixture was concentrated under reduced pressure. A mixture of the resulting residue and dimethylacetamide dimethylacetal (1 ml) was stirred at 100° C. for 1 hour. Water was added thereto, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over sodium sulfate and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography (hexane:ethyl acetate=1:1) to obtain 50 mg of the desired product as a white crystal.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06875770B2
Quelldatensatzuspto-grants-2005_04
ORD IDord-df16cd957b9742c8a68b579f24a7ff3b
Quellennotizuspto-grants-2005_04