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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 521665Erstellt: 24. Oktober 2026

Tetrahydrofuran → 2-(2-Ethylsulfanylphenyl)-4-methyl-7-trifluoromethylquinazoline

https://huagongshe.com/de/reaction/521665

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktN-methyl-2-pyrrolidoneHCID 13387—
Edukt4-Chloro-2-(2-ethylsulfanylphenyl)-7-trifluoromethylquinazolineHCID 118205819—
EduktHCID 178418573HCID 178418573—
KatalysatorFerric acetylacetonateHCID 5483663—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-(2-Ethylsulfanylphenyl)-4-methyl-7-trifluoromethylquinazolineHCID 118205822—

Reaktionsschritte

2.1 ml of methylmagnesium bromide (a 1 M THF solution) was added to a mixture of 380 mg of 4-chloro-2-(2-ethylsulfanylphenyl)-7-trifluoromethylquinazoline, 72 mg of iron(III) acetylacetonate, 8 ml of THF and 0.8 ml of NMP, and the mixture was stirred at room temperature for 1 hour. Ethyl acetate and water were added to the reaction mixture, and the mixture was filtered. The aqueous layer of the filtrate was extracted with ethyl acetate, combined with the organic layer of the filtrate, sequentially washed with 0.5 N hydrochloric acid, water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The mixture was concentrated under reduced pressure, and the resulting residue was applied to a silica gel column chromatography to obtain 123 mg of 2-(2-ethylsulfanylphenyl)-4-methyl-7-trifluoromethylquinazoline (Compound of Present Invention 13).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09328121B1
Quelldatensatzuspto-grants-2016_05
ORD IDord-93135b4fd11e4d62bfc95a20d705c658
Quellennotizuspto-grants-2016_05