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HRID 1814100Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/1814100

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1-Dimethoxyethyl(dimethyl)amineHCID 87835—
Edukt1-(4-Fluorobenzyl)-5-methanesulfonylindole-2-carboxamideHCID 22504369—
Produkt1-(4-Fluorobenzyl)-5-methanesulfonyl-2-(3-methyl-[1,2,4]oxadiazol-5-yl)indoleHCID 12094553—

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

A mixture of 1-(4-fluorobenzyl)-5-methanesulfonylindole-2-carboxamide (63 mg) and dimethylacetamide dimethylacetal (1 ml) was stirred at 110° C. for 1 hour. The reaction mixture was concentrated under reduced pressure. A mixture of the resulting residue, hydroxylamine hydrochloride (25 mg), a 2N aqueous sodium hydroxide solution (0.18 ml), 1,4-dioxane (0.4 ml) and acetic acid (0.4 ml) was stirred at 90° C. for 2 hours. 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-89192e409dbb4128a0dfdd7d17f223aa
Quellennotizuspto-grants-2005_04