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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 346546생성일: 2026년 10월 25일

Water → tert-Butyl 4-(((4-((4-bromo-2-fluorophenyl)amino)-6-methoxyquinazolin-7-yl)oxy)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/346546

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물1-(tert-Butoxycarbonyl)-4-((p-toluenesulfonyloxy)methyl)piperidineHCID 10642851—
반응물4-[(4-Bromo-2-fluorophenyl)amino]-6-methoxy-7-quinazolinolHCID 135503852—
용매DimethylformamideHCID 6228—
생성물tert-Butyl 4-(((4-((4-bromo-2-fluorophenyl)amino)-6-methoxyquinazolin-7-yl)oxy)methyl)piperidine-1-carboxylateHCID 1104999979%

반응 단계

Potassium carbonate (414 mg, 3 mmol) was added to a suspension of 4-(4-bromo-2-fluoroanilino)-7-hydroxy-6-methoxyquinazoline (546 mg, 1.5 mmol) in DMF (5 ml). After stirring for 10 minutes at ambient temperature, 1-(tert-butoxycarbonyl)-4-(4-methylphenylsulphonyloxymethyl)piperidine (636 mg, 1.72 mmol) was added and the mixture was heated at 95° C. for 2 hours. After cooling, the mixture was poured onto cooled water (20 ml). The precipitate was collected by filtration, washed with water, and dried under vacuum to give 4-(4-bromo-2-fluoroanilino)-7-(1-(tert-butoxycarbonyl)piperidin-4-ylmethoxy)-6-methoxyquinazoline (665 mg, 79%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07173038B1
출처 데이터셋uspto-grants-2007_02
ORD IDord-13efda41b1ca4c5182df8e333cec06fd
출처 메모uspto-grants-2007_02