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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 521665생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/521665

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물N-methyl-2-pyrrolidoneHCID 13387—
반응물4-Chloro-2-(2-ethylsulfanylphenyl)-7-trifluoromethylquinazolineHCID 118205819—
반응물HCID 178418573HCID 178418573—
촉매Ferric acetylacetonateHCID 5483663—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물2-(2-Ethylsulfanylphenyl)-4-methyl-7-trifluoromethylquinazolineHCID 118205822—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09328121B1
출처 데이터셋uspto-grants-2016_05
ORD IDord-93135b4fd11e4d62bfc95a20d705c658
출처 메모uspto-grants-2016_05