HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → N-(5-cyano-2-methylsulfanyl-pyrimidin-4-yl)-N-methyl-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-(5-cyano-2-methylsulfanyl-pyrimidin-4-yl)-acetamide | HCID 57929456 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | N-(5-cyano-2-methylsulfanyl-pyrimidin-4-yl)-N-methyl-acetamide | HCID 57929481 | 72% |
Reaction Steps
To a solution of N-(5-cyano-2-methylsulfanyl-pyrimidin-4-yl)-acetamide (562 mg, 2.70 mmol) and methyl iodide (1.7 mL, 27.0 mmol) in anhydrous DMSO (14 mL) was added NaH (60% wt. dispersion in mineral oil, 130 mg, 3.23 mmol) at 0° C. The reaction mixture was stirred at RT for 16 h and was then quenched by adding water (50 mL). The resulting mixture was extracted with EtOAc (2×100 mL). The combined organic layers were washed with brine (2×100 mL), dried over MgSO4, filtered, and concentrated under reduced pressure. The crude residue was purified by flash chromatography (from 0 to >33% EtOAc/hexane in 5 min.) to afford 431 mg (72% yield) of N-(5-cyano-2-methylsulfanyl-pyrimidin-4-yl)-N-methyl-acetamide as an off-white solid. MS=223 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08268840B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-bff7b245a6974a6393aa42a5b22fc82d |
| Source note | uspto-grants-2012_09 |