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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1008340생성일: 2026년 10월 25일

Chloroform → 4-{[7-(Benzyloxy)-6-methoxy-4-quinazolinyl]oxy}-2-chloroaniline

https://huagongshe.com/reaction/1008340

반응식

참여 물질

역할이름HCID투입량
반응물ChloroformHCID 6212—
반응물Sodium HydroxideHCID 14798—
반응물7-(Benzyloxy)-4-chloro-6-methoxyquinazolineHCID 10661998—
반응물4-Amino-3-chlorophenol hydrochlorideHCID 12598190—
촉매Tetrabutylammonium ChlorideHCID 70681—
용매AcetoneHCID 180—
용매WaterHCID 962—
생성물4-{[7-(Benzyloxy)-6-methoxy-4-quinazolinyl]oxy}-2-chloroanilineHCID 2266723290%

반응 단계

7-(Benzyloxy)-4-chloro-6-methoxyquinazoline (30.0 g) and tetrabutylammonium chloride (13.9 g) were dissolved in acetone (400 ml), and the solution was stirred at room temperature. A solution of 4-amino-3-chlorophenol hydrochloride (36.0 g) in a 20% aqueous sodium hydroxide solution (64 ml) was added thereto. The mixture was then heated under reflux for 3 hr. The reaction solution was cooled to room temperature, and chloroform and water were added to the cooled reaction solution, followed by extraction with chloroform. The extract was washed with a saturated aqueous sodium hydrogencarbonate solution and saturated brine and was then dried over anhydrous sodium sulfate. Next, sodium sulfate was removed, and the solvent was then removed by distillation. The residue was washed with methanol, and the washed solid was subjected to evaporation to dryness in vacuo through a vacuum pump to give 36.6 g (yield 90%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06797823B1
출처 데이터셋uspto-grants-2004_09
ORD IDord-2f79078892f0406ba85cbcd90b3c5a14
출처 메모uspto-grants-2004_09