돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1469743생성일: 2026년 10월 25일

Water → N-(2-fluoro-5-(trifluoromethyl)phenyl)-8-nitroquinazolin-4-amine

https://huagongshe.com/reaction/1469743

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2-Fluoro-5-(trifluoromethyl)anilineHCID 136349—
반응물4-Chloro-8-nitroquinazolineHCID 11458471—
용매TetrahydrofuranHCID 8028—
생성물N-(2-fluoro-5-(trifluoromethyl)phenyl)-8-nitroquinazolin-4-amineHCID 7167804698.6%

반응 단계

A solution of 4-chloro-8-nitroquinazoline (Intermediate-7, step-2, 150 mg, 0.72 mmol) and 2-fluoro-5-(trifluoromethyl)aniline (387 mg, 2.16 mmol) in THF (4 mL) was heated at 50° C. for 2 h. Then water was added to the reaction mixture and it was extracted with EtOAc. The organic layer was washed with brine, separated, dried, filtered and concentrated. The residue was purified by column chromatography to afford 250 mg of the title product. 1H NMR (300 MHz, DMSO d6): δ 10.46 (s, 1H), 8.74-8.71 (d, J=8.7 Hz, 1H), 8.63 (s, 1H), 8.43-8.40 (d, J=7.2 Hz, 1H), 8.01 (d, 1H), 7.86-7.81 (m, 2H), 7.66-7.63 (t, J=9.3 Hz, 1H); MS [M+H]+: 353.14.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09006257B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-9052b9a546cd4f4abe4e8d8b7c931ab9
출처 메모uspto-grants-2015_04