HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Peroxide → 7-Chloro-2-(2,6-dichlorophenyl)-2H-pyrazolo[4,3-c]pyridine-5-oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | 7-Chloro-2-(2,6-dichlorophenyl)-2H-pyrazolo[4,3-c]pyridine | HCID 69671438 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Catalyst | HCID 178477782 | HCID 178477782 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-Chloro-2-(2,6-dichlorophenyl)-2H-pyrazolo[4,3-c]pyridine-5-oxide | HCID 69671692 | 89% |
Reaction Steps
To a solution of 7-chloro-2-(2,6-dichlorophenyl)-2H-pyrazolo[4,3-c]pyridine (2.7 g, 9.0 mmol) and methyltrioxorhenium (31 mg, 0.09 mmol) in DCM (6 mL) was added hydrogen peroxide (30% aq., 1.75 mL, 18.0 mmol) and the resulting mixture stirred at room temperature for 18 hours. A catalytic amount of MnO2 was added to the mixture and stirring was continued for 1 hour. The reaction mixture was concentrated under reduced pressure. The residue was triturated in toluene to afford the title compound as a beige solid (2.5 g, 89% yield). LCMS (Method D): RT=2.57 min, m/z: 314 [M+H+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09309240B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-37b6a6f2f8fc41b5882ba09611e0de6b |
| Source note | uspto-grants-2016_04 |