HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 67383868, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium ethanethiolate | HCID 4459711 | — |
| Reactant | HCID 67383776 | HCID 67383776 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67383868 | HCID 67383868 | — |
Reaction Steps
To a solution of methyl 7-(ethyloxy)-6-fluoro-3-methyl-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate (9.35 g, 22.95 mmol) in dimethyl sulfoxide (150 mL) was added sodium ethanethiolate (6.44 g, 68.9 mmol) and the resulting mixture was stirred at room temperature overnight. Iodomethane (7.18 mL, 115 mmol) was added, and the mixture was stirred for 2 h. The mixture was diluted with water and extracted with methylene chloride. The organic extracts were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo to afford methyl 7-(ethyloxy)-6-(ethylthio)-3-methyl-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate. This material was used without further purification. MS (m/z) 450.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08658636B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-e3ada61207a84f969e35b4c23d45e15a |
| Source note | uspto-grants-2014_02 |