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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 467597생성일: 2026년 10월 24일

Acetic Acid → 7-Fluoroquinazolin-4(3H)-one

https://huagongshe.com/ko/reaction/467597

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물FormamidineHCID 68047—
반응물4-Fluoroanthranilic acidHCID 2724967—
반응물4-Chloro-7-fluoro-6-nitroquinazolineHCID 10609358—
용매2-MethoxyethanolHCID 8019—
생성물7-Fluoroquinazolin-4(3H)-oneHCID 135398496—

반응 단계

4-Chloro-7-fluoro-6-nitroquinazoline (7) can be prepared by methods similar to those described in J. Med. Chem. 1996, 39, 918-928. Generally, 2-amino-4-fluoro-benzoic acid (1) can be reacted with formamidine (2) and acetic acid (3) in the presence of 2-methoxyethanol to provide 7-Fluoro-3H-quinazolin-4-one (4). The 7-fluoro-3H-quinazolin-4-one (4) can then be nitrated to 7-fluoro-6-nitro-3H-quinazolin-4-one (5), which can be treated with thionyl chloride to yield 4-chloro-6-nitro-7-fluoro-3H-quinazoline (6). The 4-chloro-quinazoline compound (6) can be combined with a desirably substituted aniline, represented above by 4-fluoro-3-chloro-aniline, in the presence of a tertiary amine and isopropanol to provide the 4-anilino-6-nitro-7-fluoro-quinazoline (7).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08623883B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-5939c849420149fa8a0b323f9319daef
출처 메모uspto-grants-2014_01