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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7629생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/7629

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Sodium HydroxideHCID 14798—
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물HCID 21991771HCID 21991771—
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—
생성물2-[7-(3-Fluoro-benzyloxy)-2-methyl-4-oxo-4H-quinazolin-3-yl]-acetamideHCID 1002018065%

반응 단계

4-(3-Fluoro-benzyloxy)-2-nitro-benzoic acid: A mixture of 4-(3-fluorobenzyloxy)-2-nitro-benzoic acid (3-fluoro-benzyl) ester and 4-(3-fluoro-benzyloxy)-2-nitro-benzoic acid methyl ester (14.0 g, 35.0 mmol) in THF (120 mL) and water (120 mL), containing lithium hydroxide monohydrate (2.94 g, 70.1 mmol) was stirred at rt for 48 h. Then the mixture was poured into sodium hydroxide (2 N, 50 mL) and then the mixture extracted with diethyl ether (3×150 mL). The aqueous phase was then adjusted to pH 2 with HCl. Then the mixture was poured into sodium hydroxide (2 N, 50 mL) and the aqueous phase was then adjusted to pH 5.2 with HCl then the mixture extracted with diethyl ether (3×100 mL). The combined extracts were then washed with brine (100 mL) dried and evaporated to afford title compound (6.6 g, 65%) as a light yellow solid. MS: m/e=290.0 (M−H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087612B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-ad3689421b0444ecba177dceb56a6917
출처 메모uspto-grants-2006_08