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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7628생성일: 2026년 10월 23일

Potassium Carbonate → 2-[7-(3-Fluoro-benzyloxy)-2-methyl-4-oxo-4H-quinazolin-3-yl]-acetamide

https://huagongshe.com/ko/reaction/7628

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물3-Fluorobenzylic alcoholHCID 68008—
반응물Methyl 4-fluoro-2-nitrobenzoateHCID 14941412—
반응물4-(3-Fluoro-benzyloxy)-2-nitro-benzoic acid methyl esterHCID 69594337—
반응물4-(3-Fluorobenzyloxy)-2-nitro-benzoic acid (3-fluoro-benzyl) esterHCID 86593646—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-[7-(3-Fluoro-benzyloxy)-2-methyl-4-oxo-4H-quinazolin-3-yl]-acetamideHCID 1002018076%

반응 조건

온도65 °C

반응 단계

4-(3-Fluoro-benzyloxy)-2-nitro-benzoic acid (3-fluoro-benzyl) ester and 4-(3-fluoro-benzyloxy)-2-nitro-benzoic acid methyl ester: A mixture of 4-fluoro-2-nitro-benzoic acid methyl ester (9.2 g, 46.3 mmol), 3-fluorobenzyl alcohol (16.7 g, 132.4 mmol) and potassium carbonate (12.8 g, 92.6 mmol) in DMF (210 mL) was heated at 65° C. for 48 h. After cooling to rt, the mixture was poured into water (400 mL), and extracted with diethyl ether (3×100 mL). The combined extracts were washed with brine (100 mL) dried and evaporated. Purification by chromatography on silica gel eluting with ethyl acetate:hexane (1:1) afforded the title compound (14.0 g, 76%) as a light yellow liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087612B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-f243056d574b4911b9c3d4786237c32f
출처 메모uspto-grants-2006_08