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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 346413생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/346413

반응식

참여 물질

역할이름HCID투입량
반응물4,5-Dichloro-2-fluoroanilineHCID 223091—
반응물4-Chloro-6-nitroquinazolineHCID 11356257—
용매IsopropanolHCID 3776—
생성물4-[(3,4-Dichloro-6-fluorophenyl)amino]-6-nitroquinazolineHCID 15480998—

반응 단계

3,4-Dichloro-6-fluoroaniline (1 equivalent, prepared as described in U.S. Pat. No. 6,126,917) was reacted with 4-chloro-6-nitroquinazoline (3.5 equivalents, prepared by reacting 6-nitroquinazoline with thionyl chloride, according to known procedures), in iso-propylalcohol. After filtration, 4-[(3,4-dichloro-6-fluorophenyl)amino]-6-nitroquinazoline (compound 1) was obtained in 60% yield. m.p.=270–271° C.; MS (m/z): 353.2, 355.2 (M+); 1H-NMR: δ=6.97 (d, 1H), 7.345 (d, 1H), 7.885 (d, 1H), 8.405 (d, 1H), 8.554 (dd, 1H), 8.8 (d, 1H) ppm. HPLC conditions: C-18 column, 55% acetate buffer, PH=3.8/45% acetonitrile, flow=1 ml/min; r.t.=7.15 minutes.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07172749B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-83e5d3a1fcd541d29990cc006885a035
출처 메모uspto-grants-2007_02