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HRID 243849作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoic acid, 2-bromo-5-fluoro-, methyl esterHCID 138875—
反応物Sodium BicarbonateHCID 516892—
反応物1H-Pyrazole-5-boronic acidHCID 11251979—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物methyl 5-fluoro-2-(1H-pyrazol-5-yl)benzoateHCID 6708667844.9%

反応条件

温度23 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653263B2
出典データセットuspto-grants-2014_02
ORD IDord-bb7166fd3d904c0d84d22df8de72cb8c
出典メモuspto-grants-2014_02