HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 3-(4-Chloro-indazol-1-yl)-1-methyl-6-trifluoromethylpyrimidine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(4-chloro-indazol-1-yl)-6-trifluoromethyl-1H-pyrimidine-2,4-dione | HCID 22614262 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(4-Chloro-indazol-1-yl)-1-methyl-6-trifluoromethylpyrimidine-2,4-dione | HCID 11450793 | 39.7% |
Reaction Steps
A mixture of 168B (100 mg, 0.3 mmol), dry acetonitril (3 mL), potassium carbonate (0.05 g, 0.33 mmol) and methyl iodide (0.1 g, 0.7 mmol) is stirred overnight at room temperature. The solids are removed by filtration. The motherliquor is concentrated under reduced pressure. The residue obtained is purified by flash chromatography (ethyl acetate/petrol ether 3/7) which yields the product as an orange semi-solid (41 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06376426B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-9c1a77e972fb40a085e49424b87461d6 |
| Source note | uspto-grants-2002_04 |