HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → HCID 68739684, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | HCID 68739064 | HCID 68739064 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Sulfite | HCID 24437 | — |
| Product | HCID 68739684 | HCID 68739684 | — |
Reaction Steps
A solution of 7-allyl-5-bromo-1-(2,4-difluorophenyl)-1H-pyrazolo[3,4-b]pyridin-6(7H)-one (265 mg, 0.724 mmol) in tert-BuOH (5 mL) and water (5 mL) at RT was treated with 4-methylmorpholine N-oxide (127 mg, 1.09 mmol) and potassium osmate dihydrate (10 mg, 0.027 mmol). The resulting mixture was allowed to stir for 16 h at RT, then diluted with an aqueous solution of sodium sulfite (10 mL) and extracted with EtOAc (3×25 mL). The organic extracts were dried over MgSO4, filtered and concentrated. The crude residue was purified on the ISCO 12 g column (0-5% MeOH:DCM) affording the title compound as a white amorphous solid. MS (ESI, pos.ion) m/z: 399.0/401.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07846944B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-05ea2388d69a43aa97d2f515b3bef084 |
| Source note | uspto-grants-2010_12 |