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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 346408생성일: 2026년 10월 25일

4,5-Dichloro-2-fluoroaniline → 4-[(3,4-Dichloro-6-fluorophenyl)amino]-6-nitroquinazoline

https://huagongshe.com/reaction/346408

반응식

참여 물질

역할이름HCID투입량
반응물4,5-Dichloro-2-fluoroanilineHCID 223091—
반응물4-Chloro-6-nitroquinazolineHCID 11356257—
생성물4-[(3,4-Dichloro-6-fluorophenyl)amino]-6-nitroquinazolineHCID 15480998—

반응 단계

In one particular, 3,4-dichloro-6-fluoroaniline is reacted with 4-chloro-6-nitroquinazoline, so as to produce 4-[(3,4-dichloro-6-fluorophenyl)amino]-6-nitroquinazoline, which is reduced, by means of an ethanolic solution of hydrazine hydrate and Raney®Nickel, so as to produce 4-[(3,4-dichloro-6-fluorophenyl)amino]-6-aminoquinazoline. Then, the 4-[(3,4-dichloro-6-fluorophenyl)amino]-6-aminoquinazoline is reacted with 4-bromocrotonyl chloride, so as to produce 4-bromo-N-{4-[(3,4-dichloro-6-fluorophenyl)amino]quinazoline-6-yl}-2-butenamide, which is then reacted with methylamine, so as to produce N-{4-[(3,4-dichloro-6-fluorophenyl)amino]quinazoline-6-yl}-4-(methylamino)-2-butenamide. The obtained methylamino derivative of the butenamide is reacted with a carbon-11 labeled methyliodide, so as to produce a carbon-11 labeled N-{4-[(3,4-dichloro-6-fluorophenyl)amino]quinazoline-6-yl}-4-(dimethylamino)-2-butenamide (carbon-11 labeled Compound 4).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07172749B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-bfff5b6aa96840d1911371df5d83a26c
출처 메모uspto-grants-2007_02