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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72482생성일: 2026년 10월 24일

3-Chlorophenol → 2-(3-(3-Chlorophenoxy)azetidin-1-yl)-5-fluoronicotinic acid

https://huagongshe.com/ko/reaction/72482

반응식

참여 물질

역할이름HCID투입량
반응물3-ChlorophenolHCID 7933—
반응물Potassium CarbonateHCID 11430—
반응물Sodium HydroxideHCID 14798—
반응물Methyl 5-fluoro-2-(3-((methylsulfonyl)oxy)azetidin-1-yl)nicotinateHCID 86697878—
용매DimethylformamideHCID 6228—
생성물2-(3-(3-Chlorophenoxy)azetidin-1-yl)-5-fluoronicotinic acidHCID 67958151—

반응 조건

온도160 °C

반응 단계

To a solution of 3-chlorophenol (0.035 ml, 0.328 mmol) in dimethylformamide (1 ml), potassium carbonate (45.42 mg, 0.328 mmol) and the reaction mixture was stirred 2 h at 80° C. Methyl 5-fluoro-2-(3-((methylsulfonyl)oxy)azetidin-1-yl)nicotinate (D71) (100 mg, 0.328 mmol) was added and the resulting reaction mixture was heated 12 h at 160° C. After cooling at room temperature 1N NaOH (0.656 ml, 0.656 mmol) was added and the reaction mixture heated 2 h at 120° C. Solvents were evaporated in vacuo and the residue was loaded on SPE-SCX cartridge (5 g). Ammonia fractions after solvent evaporation afforded a residue that was further purified by Biotage column SNAP-C18 (30 g) eluting with water/acetic acid (0.1%)/acetonitrile-acetic acid (0.1%) from 70/30 to 0/100.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08828987B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-96a034a9baf64bcea343537b99407cc2
출처 메모uspto-grants-2014_09