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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 83204생성일: 2026년 10월 23일

Sodium Chloride → 6-[3-(3-Fluoro-phenyl)-5-methyl-isoxazol-4-ylmethoxy]-nicotinic acid methyl ester

https://huagongshe.com/ko/reaction/83204

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물Sodium hydrideHCID 24758—
반응물Methyl 6-chloropyridine-3-carboxylateHCID 254249—
반응물(3-(3-Fluorophenyl)-5-methylisoxazol-4-yl)methanolHCID 67157856—
용매TetrahydrofuranHCID 8028—
생성물6-[3-(3-Fluoro-phenyl)-5-methyl-isoxazol-4-ylmethoxy]-nicotinic acid methyl esterHCID 6844189468%

반응 단계

To a suspension of sodium hydride (55% dispersion in mineral oil, 852 mg, 20 mmol) in THF (27 mL) was added a solution of [3-(3-fluoro-phenyl)-5-methyl-isoxazol-4-yl]-methanol (3.68 g, 18 mmol) in THF (54 mL) at 0° C. and the reaction mixture warmed to room temperature over 30 min. Then a solution of methyl 6-chloronicotinate (3.35 g, 20 mmol) in THF (1.5 mL) was added dropwise at 0° C. and the reaction mixture was stirred at room temperature overnight. The reaction mixture was then poured into aqueous sodium chloride (saturated) and the mixture was extracted with ethyl acetate. The combined organic layers were then washed with water and brine and then dried over sodium sulfate, filtered and evaporated. Purification by chromatography (SiO2, heptane:ethyl acetate=7:3) afforded the title compound (4.1 g, 68%) which was obtained as a white solid. MS: m/e=343.1 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846719B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-3ab663b664e245d3bc0f37b160910179
출처 메모uspto-grants-2014_09