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HRID 9182作成日:2026年10月24日

Water → 7-(2,4-Dichlorophenyl)-2-ethylpyrazolo[1,5-a]pyridine

https://huagongshe.com/ja/reaction/9182

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium CarbonateHCID 10340—
反応物2,4-Dichlorophenylboric acidHCID 21984477—
反応物7-Bromo-2-ethylpyrazolo[1,5-a]pyridineHCID 21984510—
触媒HCID 178418397HCID 178418397—
溶媒EthanolHCID 702—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物7-(2,4-Dichlorophenyl)-2-ethylpyrazolo[1,5-a]pyridineHCID 2198463597.9%

反応条件

温度80 °C

反応手順

After dissolving 7-bromo-2-ethylpyrazolo[1,5-a]pyridine (300 mg) in ethanol (2 mL) and toluene (4 mL), 2,4-dichlorophenylboric acid (508 mg), tetrakis(triphenylphosphine)palladium (0) complex (154 mg) and 2 M aqueous sodium carbonate (1.33 mL) were added and the mixture was heated and stirred at 80° C. for 3 hours under a nitrogen stream. Water was added to the reaction mixture, extraction was performed with ethyl acetate and the organic layer was washed with brine. After drying over anhydrous magnesium sulfate and filtration, the solvent was concentrated under reduced pressure, the residue was purified by silica gel column chromatography, and the title compound (380 mg) was obtained from the n-hexane:ethyl acetate (100:1) fraction as a light yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091215B2
出典データセットuspto-grants-2006_08
ORD IDord-f014e611ef1f44afbd81fa386b31f468
出典メモuspto-grants-2006_08