참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 5-[2-(Amino)ethylthio]imidazo[1,2-a]pyridine | HCID 15229369 | — |
| 반응물 | 2-Acetylsalicyloyl chloride | HCID 57361564 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 5-[2-[2-(Hydroxy)benzoylamino]ethylthio]imidazo[1,2-a]pyridine | HCID 23362977 | 56% |
반응 단계
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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05244908 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-d34a489740ed4a9e8f386753fe5c41ad |
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| 출처 메모 | uspto-grants-1993_09 |
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