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HRID 489831作成日:2026年10月27日

Potassium Phosphate, Tribasic → 5-Amino-1-(4-fluorophenyl)-4-[3-(pyridin-3-yl)benzoyl]pyrazole

https://huagongshe.com/reaction/489831

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium Phosphate, TribasicHCID 62657—
反応物3-Pyridinylboronic acidHCID 2734378—
反応物3-(1,3,2-Dioxaborinan-2-yl)pyridineHCID 4198005—
反応物5-Amino4-(3-bromobenzoyl)-1-(4-fluorophenyl)pyrazoleHCID 11451237—
溶媒1,4-DioxaneHCID 31275—
溶媒Sodium chloride; waterHCID 57417360—
生成物5-Amino-1-(4-fluorophenyl)-4-[3-(pyridin-3-yl)benzoyl]pyrazoleHCID 9950664—

反応条件

温度85 °C

反応手順

A mixture of 5-amino-4-(3-bromobenzoyl)-1-(4-fluorophenyl)pyrazole (0.9 g, 2.5 mmol) [prepared as described in Example 1 above], pyridine-3-boronic acid, 1,3-propanediol cyclic ester (0.5 g, 3 mmol), potassium phosphate (0.8 g, 3.73 mmol) and tetrakistriphosphine palladium (0.3 g, 0.25 mmol) in dioxane (20 ml) was heated at 85° C. under argon. After 16 h, the reaction mixture was cooled to room temperature and poured into brine. The product was extracted into ethyl acetate, dried over sodium sulfate and filtered. The organic layer was removed in vacuo and the residue was purified by flash chromatography (elution gradient: 40-80% ethyl acetate/hexane) to give 5-amino-1-(4-fluorophenyl)-4-[3-(pyridin-3-yl)benzoyl]pyrazole (0.50 g) which was recrystallized from ethyl acetate (mpt. 222.2-223.0).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06979693B2
出典データセットuspto-grants-2005_12
ORD IDord-f9e79f097ffd47f197aedf3dcceed4b3
出典メモuspto-grants-2005_12