HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 58541669, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Persulfate | HCID 24412 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | HCID 58541652 | HCID 58541652 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 58541669 | HCID 58541669 | — |
Reaction Steps
To a solution of 6-(4-fluorophenyl)-5-[2-(methylsulfanyl)pyrimidin-4-yl]imidazo[2,1-b][1,3]oxazole (E) (2.0 g, 6.13 mmol) in methanol (250 mL) is slowly added Oxone™ (potassium monopersulfate) (11.3 g, 18.4 mmol) in water (50 mL). The mixture is stirred at room temperature for 24 hours. The solvent is removed in vacuo and the residue dissolved in dichloromethane, washed with water, and dried over anhydrous sodium sulfate. The solids are removed by filtration and the solvent removed in vacuo. The residue is purified by silica gel column chromatography to provide 6-(4-fluorophenyl)-5-[2-(methylsulfonyl)pyrimidin-4-yl]imidazo[2,1-b][1,3]oxazole (F) (Compound XI, Table 1)) as a white solid (1.8 g, 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07902192B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-3510c02de09c41d68e482869215ca6ec |
| Source note | uspto-grants-2011_03 |