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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 634677생성일: 2026년 10월 26일

Hexane → 7-Acetoxy4-(5-benzyloxy-2-fluoro-4-methylanilino)-6-methoxyquinazoline

https://huagongshe.com/reaction/634677

반응식

참여 물질

역할이름HCID투입량
반응물HexaneHCID 8058—
반응물Thionyl ChlorideHCID 24386—
반응물5-Benzyloxy-2-fluoro-4-methylanilineHCID 21991068—
반응물7-Acetoxy-6-methoxy-3,4-dihydroquinazolin-4-oneHCID 135697905—
촉매DimethylformamideHCID 6228—
용매IsopropanolHCID 3776—
생성물7-Acetoxy4-(5-benzyloxy-2-fluoro-4-methylanilino)-6-methoxyquinazolineHCID 2126031243%

반응 단계

A mixture of 7-acetoxy-6-methoxy-3,4-dihydroquinazolin-4-one (1.69 g, 7.2 mmol), thionyl chloride (50 ml) and DMF (3 drops) was heated at reflux for 2 hours. The excess thionyl chloride was removed by evaporation and the residue azeotroped with toluene. The residue was partitioned between methylene chloride and saturated aqueous sodium hydrogen carbonate solution. The organic phase was separated, dried (MgSO4) and the solvent removed by evaporation. 5-Benzyloxy-2-fluoro-4-methylaniline (1.8 g, 7.8 mmol) in isopropanol (50 ml) was added to the residue and the mixture heated at reflux for 2 hours. The mixture was allowed to cool, hexane added and the precipitated product collected by filtration to give 7-acetoxy-4-(5-benzyloxy-2-fluoro-4-methylanilino)-6-methoxyquinazoline (1.34 g, 43%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06184225B2
출처 데이터셋uspto-grants-2001_02
ORD IDord-ebb58f8a97c24a4e87a477c597871eff
출처 메모uspto-grants-2001_02