HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5-[2-(Methylcarbamoyloxy)ethylthio]imidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | 5-[2-(Hydroxy)ethylthio]imidazo[1,2-a]pyridine | HCID 14456849 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-[2-(Methylcarbamoyloxy)ethylthio]imidazo[1,2-a]pyridine | HCID 23362817 | 85.2% |
Reaction Steps
To a solution of 5-[2-(hydroxy)ethylthio]imidazo[1,2-a]pyridine (971 mg, 5 mmoles) and trietylamine (0.91 ml, 6.53 mmoles) in methylene chloride (40 ml) was added methyl isocyanate (0.65 ml, 11 mmoles) under ice-cooling with stirring and the mixture was stirred at room temperature for 12 hours. The reaction mixture was washed with saturated saline and dried over anhydrous magnesium sulfater. After the solvent was distilled off, the residue was purified by column chromatography (eluent: methanol/chloroform=1:20) to obtain 1.07 g of the desired product (85.2%, colorless crystals).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05244908 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-38cd054a169a4254b93577d431c563a5 |
| Source note | uspto-grants-1993_09 |