関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 2,4-Piperidinedione | HCID 10887863 | — |
| 反応物 | 2-Phenylpyrazolo[1,5-a]pyridine | HCID 15620342 | — |
| 触媒 | Sulfuric Acid | HCID 1118 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | 3-(2-Oxo-1,2,5,6-tetrahydropyridin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine | HCID 15158110 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05155114 |
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| 出典データセット | uspto-grants-1992_10 |
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| ORD ID | ord-107a60501a1e4e338f58c4fd604a95cb |
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| 出典メモ | uspto-grants-1992_10 |
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