HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 7-Cyclohexyl-5-methyl-5H,7H-isoxazolo[3,4-d]pyrimidine-4,6-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-cyclohexyl-5H,7H-isoxazolo[3,4-d]pyrimidine-4,6-dione | HCID 13536943 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-Cyclohexyl-5-methyl-5H,7H-isoxazolo[3,4-d]pyrimidine-4,6-dione | HCID 12380624 | 75.5% |
Reaction Steps
In 50 ml of dimethylformamide is dissolved 1 g of the 7-cyclohexyl-5H,7H-isoxazolo[3,4-d]pyrimidine-4,6-dione obtained in Example 18, followed by addition of 800 mg of potassium carbonate and 1 ml of methyl iodide. The mixture is stirred at room temperature for 20 hours, after which the insolubles are filtered off. The filtrate is concentrated to dryness and the concentrate is dissolved in chloroform. After the insolubles are filtered off, the chloroform is removed by distillation and the residue is recrystallized from water-ethanol. By the above procedure is obtained 0.8 g of the captioned compound as pale-white platelets. melting point: 194°-197° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04129654 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-8b75c21ec81841d3bbd7d8f22f4a0bed |
| Source note | uspto-grants-1978_12 |