HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methyl-2-thiopseudourea sulfate → 4-Trifluoromethyl-2-methylthio-6-(pyridin-2-yl)pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methyl-2-thiopseudourea sulfate | HCID 75270 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 4,4,4-Trifluoro-1-(pyridin-2-yl)butane-1,3-dione | HCID 2771478 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Trifluoromethyl-2-methylthio-6-(pyridin-2-yl)pyrimidine | HCID 66593292 | 17% |
Reaction Steps
To a solution of 4,4,4-trifluoro-1-(pyridin-2-yl)butane-1,3-dione (1.0 g, 4.6 mmol) in ethanol (10 mL) was added 2-methyl-2-thiopseudourea sulfate (0.64 g, 4.6 mmol), followed by sodium ethoxide (3.0 mL of 21 wt. % solution in ethanol, 9 mmol). The mixture was heated at reflux for 9 h, then cooled to room temperature and extracted with EA. The EA was washed with water and the solvent removed under reduced pressure. The crude product was purified by column chromatography, eluting with 49:1 chloroform/MeOH, to give 4-trifluoromethyl-2-methylthio-6-(pyridin-2-yl)pyrimidine (0.21 g, 17% yield) as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08129396B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-df5cfb85256343b4a98440a4d2463762 |
| Source note | uspto-grants-2012_03 |