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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 488421생성일: 2026년 10월 25일

Water → 4-[(3-Bromophenyl)amino]-6-[(4-{N-[(tert-butyloxycarbonyl)methyl]-N-[2-(acetylsulphanyl)ethyl]amino)-1-oxo-2-buten-1-yl)-amino]-7-methoxy-quinazoline

https://huagongshe.com/reaction/488421

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium ethanethioateHCID 23670855—
반응물4-[(3-bromophenyl)amino]-6-[(4-(N-[(tert-butyloxycarbonyl)methyl]-N-[2-(methylsulphonyloxy)ethyl]amino}-1-oxo-2-buten-1-yl)amino]-7-methoxy-quinazolineHCID 57214443—
용매DimethylformamideHCID 6228—
생성물4-[(3-Bromophenyl)amino]-6-[(4-{N-[(tert-butyloxycarbonyl)methyl]-N-[2-(acetylsulphanyl)ethyl]amino)-1-oxo-2-buten-1-yl)-amino]-7-methoxy-quinazolineHCID 73879451—

반응 단계

34 mg of potassium thioacetate are added to 150 mg of 4-[(3-bromophenyl)amino]-6-[(4-(N-[(tert-butyloxycarbonyl)methyl]-N-[2-(methylsulphonyloxy)ethyl]amino}-1-oxo-2-buten-1-yl)amino]-7-methoxy-quinazoline in 1 ml of dimethylformamide at ambient temperature. The reaction mixture is stirred overnight at ambient temperature and then combined with water for working up. The aqueous phase is separated off and extracted with ethyl acetate, the combined organic phases are dried over magnesium sulphate and freed from solvent in the rotary evaporator. Yield: 20 mg (14% of theory), Rf value: 0.62 (silica gel, ethyl acetate/methanol=15:1) Mass spectrum (EI): m/z=643, 645 [M]+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06972288B1
출처 데이터셋uspto-grants-2005_12
ORD IDord-96fe93f0c8294e8a818701511fb4c946
출처 메모uspto-grants-2005_12