HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081726Generated: October 26, 2026
Triethylamine → 5-[2-[2-(Hydroxy)benzoylamino]ethylthio]imidazo[1,2-a]pyridine
https://huagongshe.com/reaction/1081726
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-[2-(Amino)ethylthio]imidazo[1,2-a]pyridine | HCID 15229369 | — |
| Reactant | 2-Acetylsalicyloyl chloride | HCID 57361564 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-[2-[2-(Hydroxy)benzoylamino]ethylthio]imidazo[1,2-a]pyridine | HCID 23362977 | 56% |
Reaction Steps
To a solution of 5-[2-(amino)ethylthio]imidazo[1,2-a]pyridine (3.87 g, 20 mmoles) and triethylamine (5.58 ml, 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 strirring 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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05587383 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-1c05986e8943460fbfcf26be8e32b5fa |
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| Source note | uspto-grants-1996_12 |
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