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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1838562생성일: 2026년 10월 27일

Methanol → 4-(4-Bromo-2-fluoroanilino)6-methoxy-7-(3-methylsulphonylpropoxy)quinazoline

https://huagongshe.com/reaction/1838562

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물4-(4-Bromo-2-fluoroanilino)-6-methoxy-7-(3-methylthiopropoxy)quinazolineHCID 22478281—
반응물Potassium hydroxy sulfiteHCID 23707502—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물4-(4-Bromo-2-fluoroanilino)6-methoxy-7-(3-methylsulphonylpropoxy)quinazolineHCID 1875344773%

반응 단계

A solution of OXONE, (trade mark of E.I. du Pont de Nemours & Co.,Inc), (800 mg) in water (4.5 ml) was added to a solution of 4-(4-bromo-2-fluoroanilino)-6-methoxy-7-(3-methylthiopropoxy)quinazoline (300 mg, 0.66 mmol), (prepared as described in Example 31), in methanol (15 ml) and the mixture was stirred for 4 hours at ambient temperature. The mixture was diluted with methylene chloride, was washed with aqueous sodium hydrogen carbonate solution, dried (MgSO4) and the solvent was removed by evaporation. The residue was triturated with ethyl acetate/hexane, collected by filtration and dried to give 4-(4-bromo-2-fluoroanilino)-6-methoxy-7-(3-methylsulphonylpropoxy)quinazoline (235 mg, 73%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06673803B2
출처 데이터셋uspto-grants-2004_01
ORD IDord-b2450a5c16e2458e99ab36c13258c680
출처 메모uspto-grants-2004_01