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HRID 243849생성일: 2026년 10월 24일

Benzoic acid, 2-bromo-5-fluoro-, methyl ester → methyl 5-fluoro-2-(1H-pyrazol-5-yl)benzoate

https://huagongshe.com/ko/reaction/243849

반응식

참여 물질

역할이름HCID투입량
반응물Benzoic acid, 2-bromo-5-fluoro-, methyl esterHCID 138875—
반응물Sodium BicarbonateHCID 516892—
반응물1H-Pyrazole-5-boronic acidHCID 11251979—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물methyl 5-fluoro-2-(1H-pyrazol-5-yl)benzoateHCID 6708667844.9%

반응 조건

온도23 °C

반응 단계

Methyl 2-bromo-5-fluorobenzoate (1.0 g, 4.2 mmol) and (1H-pyrazol-5-yl)boronic acid (485 mg, 4.6 mmol) were combined and dissolved in degassed DME (15 ml) then treated with NaHCO3 (706 mg, 8.4 mmol) in water and the reaction purged with bubbling N2 for 5 minutes. The reaction was treated with Pd(PPh3)4 (243 mg (0.2 mmol) and then purged with bubbling for 5 minutes in a sealed vessel and then heated to reflux for 2 h. The reaction mixture was cooled to 23° C., filtered, and solid rinsed with EtOAc. The organic layers were separated, dried and concentrated. Purification via FCC (ethyl acatate/hexanes, 0-30%) afforded methyl 5-fluoro-2-(1H-pyrazol-5-yl)benzoate (415 mg, 44%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653263B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-bb7166fd3d904c0d84d22df8de72cb8c
출처 메모uspto-grants-2014_02