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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 279574생성일: 2026년 10월 25일

4-Chloro-2-fluorophenol → 7-Benzyloxy-4-(4-chloro-2-fluorophenoxy)-6-methoxyquinazoline

https://huagongshe.com/reaction/279574

반응식

참여 물질

역할이름HCID투입량
반응물4-Chloro-2-fluorophenolHCID 181975—
반응물7-(Benzyloxy)-4-chloro-6-methoxyquinazoline hydrochlorideHCID 22030836—
용매PyridineHCID 1049—
생성물7-Benzyloxy-4-(4-chloro-2-fluorophenoxy)-6-methoxyquinazolineHCID 2187482577%

반응 단계

4-Chloro-2-fluoro-phenol (264 mg, 1.8 mmol) was added to a solution of 7-benzyloxy-4-chloro-6-methoxyquinazoline hydrochloride (506 mg, 1.5 mmol), (prepared as described for the starting material in Example 1), in pyridine (8 ml) and the mixture heated at reflux for 45 minutes. The solvent was removed by evaporation and the residue partitioned between ethyl acetate and water. The organic layer was washed with 0.1M hydrochloric acid, water and brine, dried (MgSO4) and the solvent removed by evaporation. The solid residue was triturated with petroleum ether and the crude product collected by filtration and purified by flash chromatography eluting with methylene chloride/ether (9/1) to give 7-benzyloxy-4-(4-chloro-2-fluorophenoxy)-6-methoxyquinazoline (474 mg, 77%) as a cream solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06362336B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-8df83238fa9745758f57a2fcb0296b6a
출처 메모uspto-grants-2002_03