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HRID 466011作成日:2026年10月25日

Sodium Bicarbonate → 3-(2-Oxo-1,2,5,6-tetrahydropyridin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/466011

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物2,4-PiperidinedioneHCID 10887863—
反応物2-Phenylpyrazolo[1,5-a]pyridineHCID 15620342—
触媒Sulfuric AcidHCID 1118—
溶媒Acetic AcidHCID 176—
生成物3-(2-Oxo-1,2,5,6-tetrahydropyridin-4-yl)-2-phenylpyrazolo[1,5-a]pyridineHCID 15158110—

反応条件

温度135 °C

反応手順

A mixture of 2-phenylpyrazolo[1,5-a]pyridine (0.50 g, 2,4-piperidinedione (0.292 g), concentrated sulfuric acid (1 drop) and acetic acid (0.5 ml) was heated at 135° C. for 13.5 hours. A saturated aqueous solution of sodium hydrogen carbonate (20 ml) was added to the reaction mixture and the mixture was extracted with chloroform (20 ml×2). The combined extract was washed with a saturated aqueous solution of sodium chloride (20 ml) and dried over magnesium sulfate. The solvent was evaporated in vacuo. The residue was purified by column chromatography on silica gel using a mixture of chloroform and ethyl acetate (9:1) and recrystallized from ethyl acetate to give crystals of 3-(2-oxo-1,2,5,6-tetrahydropyridin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05155114
出典データセットuspto-grants-1992_10
ORD IDord-107a60501a1e4e338f58c4fd604a95cb
出典メモuspto-grants-1992_10