HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium peroxymonosulphate → Methyl 6-(2,6-difluoro-4-(methylsulfinyl)phenyl)-5-fluoropicolinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium peroxymonosulphate | HCID 10313463 | — |
| Reactant | Methyl 6-(2,6-difluoro-4-(methylthio)phenyl)-5-fluoropicolinate | HCID 66652477 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 6-(2,6-difluoro-4-(methylsulfinyl)phenyl)-5-fluoropicolinate | HCID 70655092 | 23.5% |
Reaction Steps
To a solution of methyl 6-[2,6-difluoro-4-(methylthio)phenyl]-5-fluoropyridine-2-carboxylate (150 mg, 0.479 mmol) in DCM (3.0 mL) was added potassium peroxymonosulfate (147 mg, 0.958 mmol) at room temperature. The reaction mixture was stirred at room temperature for 2 h. The solution was partitioned between EtOAc and water. The organic layer was dried, filtered. The filtrate was concentrated and then purified by silica gel column chromatography using CombiFlash® (0 to 100% EtOAc in hexanes) to give the sub-title compound as a white powder (37 mg, 23%). LCMS calc. for C14H11F3NO3S (M+H)+: m/z=330.0. Found: 330.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09200004B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-0469b486c1ca45c284decceab0b7368a |
| Source note | uspto-grants-2015_12 |