HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 7-Chloro-4-quinolinyl methyl(phenyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-methyl-3-(methyl-phenyl-carbamoyl)-3H-imidazol-1-ium iodide | HCID 10947884 | — |
| Reactant | HCID 178516426 | HCID 178516426 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7-Chloro-4-quinolinyl methyl(phenyl)carbamate | HCID 749790 | 93% |
Reaction Steps
A solution of 7-chloro-4-hydroxyquinoline (0.54 g, 3.00 mmol), 1-methyl-3-(methyl-phenyl-carbamoyl)-3H-imidazol-1-ium iodide (1.03 g, 3.00 mmol) and triethylamine (0.42 ml, 3.00 mmol) in acetonitrile (15 ml) was stirred at room temperature for 18 hours. The solvent was evaporated in vacuo and the residue was purified by flash column chromatography (SiO2, ethyl acetate:heptane (40:60)) yielding the title compound (0.87 g, 93% yield) as a colourless oil which solidified upon standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07279470B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-99aae05660524676adccca37a4b4483a |
| Source note | uspto-grants-2007_10 |