HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 59564353, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | HCID 59564546 | HCID 59564546 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 59564353 | HCID 59564353 | — |
Reaction Steps
To a solution of 2-(3,5-dimethyl-pyrazol-1-yl)-1-{4-[2-(2-methylsulfanyl-pyrimidin-5-yl)-phenyl]-piperazin-1-yl}-ethanone (210 mg, 0.497 mmol) in THF (5 mL) is added a solution of oxone (611 mg, 0.994 mmol) in water (5 mL). The mixture is allowed to stir at room temperature for 4 h. Water (10 mL) is added and the mixture is extracted with EtOAc 3×. The organic extracts are washed with water, brine, dried (Na2SO4) and concentrated. The residue is re-dissolved in dichloromethane (3 mL) and loaded on a 10 g Biotage SNAP column and eluted with 100% EtOAc to provide 2-(3,5-dimethyl-pyrazol-1-yl)-1-{4-[2-(2-methanesulfonyl-pyrimidin-5-yl)-phenyl]-piperazin-1-yl}-ethanone (102 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08450317B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-8bdd9c50a9564f36a0ea36aa3a6050b4 |
| Source note | uspto-grants-2013_05 |