HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 5-Bromo-3-(2-(methylsulfonyl)pyrimidin-4-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | 5-Bromo-3-(2-(methylthio)pyrimidin-4-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole | HCID 67959721 | — |
| Product | 5-Bromo-3-(2-(methylsulfonyl)pyrimidin-4-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole | HCID 67959720 | — |
Reaction Steps
To a RT slurry of 5-bromo-3-(2-(methylthio)pyrimidin-4-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (0.855 g, 2.109 mmol) in MeOH (40 mL) was added oxone, monopersulfate compound (6.46 g, 10.51 mmol, Aldrich) and the reaction was stirred overnight. The reaction mixture was concentrated to ˜50% volume and diluted with water. The slurry was neutralized with 5 N NaOH and the solids were filtered, washed consecutively with water and MeOH, and dried in vacuo to give 795 mg of a light-yellow amorphous solid. m/z: 437.9, 439.0 [M+1].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09090593B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-11eabbd11d34485eb77f4dd69e413a77 |
| Source note | uspto-grants-2015_07 |