関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 5-[2-(Amino)ethylthio]imidazo[1,2-a]pyridine | HCID 15229369 | — |
| 反応物 | 2-Acetylsalicyloyl chloride | HCID 57361564 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 5-[2-[2-(Hydroxy)benzoylamino]ethylthio]imidazo[1,2-a]pyridine | HCID 23362977 | 56% |
反応手順
To a solution of 5-[2-(amino)ethylthio]imidazo[1,2-a]pyridine (3.87 g, 20 mmoles) and triethylamine (5.58 ml, 40 mmoles) in methylene chloride (200 ml) was added o-acetylsalicyloyl chloride (4.77 g, 24 mmoles) under ice-cooling with stirring and the mixture was stirred at room temperature for 30 minutes. After the solvent was distilled off, ethanol (60 ml) and 1N NaOH (40 ml) were added to the residue, followed by stirring for 1 hour. 1N HCl (40 ml) was added and ethanol was distilled off, and then the residue was extracted with chloroform and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography (eluent: ethyl acetate/ethanol=10:1) to obtain 3.51 g of the desired product (56.0%, colorless solid).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05244908 |
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| 出典データセット | uspto-grants-1993_09 |
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| ORD ID | ord-d34a489740ed4a9e8f386753fe5c41ad |
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| 出典メモ | uspto-grants-1993_09 |
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