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HRID 1161145Erstellt: 24. Oktober 2026

Lithium Carbonate → 1-{2-Hydroxy-4-[3-(3-iodo-benzyl)-[1,2,4]oxadiazol-5-ylmethoxy]-3-methyl-phenyl}-ethanone

https://huagongshe.com/de/reaction/1161145

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktLithium CarbonateHCID 11125—
Edukt3-(3-Amino-1,2,4-oxadiazol-5-yl)-1-azabicyclo(2.2.1)heptaneHCID 163938—
Edukt1-(2,4-Dihydroxy-3-methylphenyl)ethan-1-oneHCID 592139—
Edukt5-Chloromethyl-3-(3-iodo-benzyl)-[1,2,4]oxadiazoleHCID 57438412—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-{2-Hydroxy-4-[3-(3-iodo-benzyl)-[1,2,4]oxadiazol-5-ylmethoxy]-3-methyl-phenyl}-ethanoneHCID 6669962153,8%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

Add lithium carbonate (49 mg, 0.66 mmol) and 5-chloromethyl-3-(3-iodo-benzyl)-[1,2,4]oxadiazole (200 mg, 0.60 mmol) to a solution of 1-(2,4-dihydroxy-3-methyl-phenyl)-ethanone (110 mg, 0.66 mmol) in anhydrous dimethylformamide (20 mL) 4]oxadiazole (200 mg, 0.60 mmol). Heat the reaction mixture at 60° C. overnight. Cool the reaction mixture to RT, pour into H2O, and extract with diethyl ether (3×). Combine the organic layers, wash with brine, dry over sodium sulfate, and concentrate to provide the title compound (150 mg). LC-MS (m/e): 463 (M−1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07816523B2
Quelldatensatzuspto-grants-2010_10
ORD IDord-0894953b1a8b4ccaaaacef27a1a9f109
Quellennotizuspto-grants-2010_10