HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl chloroformate → 5-[2-(Methoxycarbonylamino)ethylthio]imidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-[2-(Amino)ethylthio]imidazo[1,2-a]pyridine | HCID 15229369 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-[2-(Methoxycarbonylamino)ethylthio]imidazo[1,2-a]pyridine | HCID 9816411 | 66.9% |
Reaction Steps
To a solution of 5-[2-(amino)ethylthio]imidazo[1,2-a]pyridine (1.93 g, 10 mmoles) and triethylamine (1.53 ml, 11 mmoles) in methylene chloride (30 ml) was added methyl chloroformate (0.77 ml, 10 mmoles) under ice-cooling with stirring and the mixture was stirred at room temperature for 20 minutes. The reaction mixture was washed in turn with an aqueous sodium bicarborate solution and water, dried over anhydrous magnesium sulfate, and then the solvent was distilled off. The residue was purified by column chromatography (eluent: ethanol/ethyl acetate=1:10) to obtain 1.68 g of the desired product (66.9%, colorless crystals).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05244908 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-a1682d3d63114f3888105607aebf2126 |
| Source note | uspto-grants-1993_09 |