HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 72944631, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 72696793 | HCID 72696793 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 72944631 | HCID 72944631 | — |
Reaction Steps
0.03 g of 60% sodium hydride (oil-based) and 0.14 g of methyl iodide were added to a mixture of 0.15 g of 2-ethylsulfanyl-N-(5-trifluoromethyl-pyridin-2-yl)-benzamide and 2 mL of THF, and the mixture was stirred at room temperature for 5 hours. A saturated aqueous sodium bicarbonate solution was poured to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure, and the resulting residue was applied to a silica gel column chromatography to obtain 0.10 g of 2-ethylsulfanyl-N-methyl-N-(5-trifluoromethyl-pyridin-2-yl)-benzamide (hereinafter, referred to as Compound of Present Invention 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09392791B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-ddde53dd7e514c229206177247561e3c |
| Source note | uspto-grants-2016_07 |