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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1639312생성일: 2026년 10월 27일

Ethyl bromoacetate → Ethyl {3-[(4-bromo-2-fluorophenyl)methyl]-7-chloro-2,4-dioxo-3,4-dihydroquinazolin-1(2H)-yl}acetate

https://huagongshe.com/reaction/1639312

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl bromoacetateHCID 7748—
반응물Potassium CarbonateHCID 11430—
반응물3-(4-bromo-2-fluorobenzyl)-7-chloro-2,4(1H,3H)-quinazolinedioneHCID 14423799—
용매DimethylformamideHCID 6228—
생성물Ethyl {3-[(4-bromo-2-fluorophenyl)methyl]-7-chloro-2,4-dioxo-3,4-dihydroquinazolin-1(2H)-yl}acetateHCID 1143134089.8%

반응 단계

A solution of 3-(4-bromo-2-fluorobenzyl)-7-chloro-1,2,3,4-tetrahydro-2,4-dioxoquinazoline (500 mg), ethyl bromoacetate (218 mg) and potassium carbonate (360 mg) in N,N-dimethylformamide (5 ml) was stirred at 30° C. for 30 minutes. The solution was evaporated and the residue was dissolved in ethyl acetate. The solution was washed in turn with 0.5N aqueous hydrochloric acid and water, and then dried over magnesium sulfate. The solvent was removed in vacuo to give a crystalline residue, which was crystallized from a mixture of ethyl acetate and n-hexane to give ethyl 2-[3-(4-bromo-2-fluorobenzyl)-7-chloro-1,2,3,4-tetrahydro-2,4-dioxoquinazolin-1-yl]acetate (550 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04883800
출처 데이터셋uspto-grants-1989_11
ORD IDord-da1caf00f70f43c8b47dc88d6a12ba1e
출처 메모uspto-grants-1989_11