돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7627생성일: 2026년 10월 23일

Hydrochloric Acid → 2-[7-(4-Fluoro-benzyloxy)-4-oxo-4H-quinazolin-3-yl]-acetamide

https://huagongshe.com/ko/reaction/7627

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium hydrideHCID 24758—
반응물4-Fluorobenzylic alcoholHCID 68022—
반응물7-Fluoroquinazolin-4(3H)-oneHCID 135398496—
반응물7-(4-Fluoro-benzyloxy)-3H-quinazolin-4-oneHCID 135752715—
용매DimethylformamideHCID 6228—
생성물2-[7-(4-Fluoro-benzyloxy)-4-oxo-4H-quinazolin-3-yl]-acetamideHCID 1008781366%

반응 조건

온도140 °C

반응 단계

7-(4-Fluoro-benzyloxy)-3H-quinazolin-4-one: A mixture of sodium hydride (55%, 3.2 g, 73 mmol), 4-fluorobenzyl alcohol (9.2 g, 73 mmol) and 7-fluoro-3H-quinazolin-4-one (3.0 g, 18 mmol) in DMF (75 mL) was heated at 140° C. for 2 h. The resulting suspension was cooled to rt and the mixture acidified to pH 3 with HCl (conc.). The resulting precipitate was then filtered off, washed with water and diethylether. Partial purification by chromatography on silica gel eluting with ethyl acetate:hexane (2:1) afforded the title compound (3.2 g, 66%) as an off-white solid. MS: m/e=271.3 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087612B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-02ebb08f2555436889139e7598c8df89
출처 메모uspto-grants-2006_08