Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | HCID 67539587 | HCID 67539587 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67541052 | HCID 67541052 | 71% |
Reaction Steps
N-[7-(2-Methylthiophenylamino)-6-(4-phenylpiperidine-1-carbonyl)pyrazolo[1,5-a]pyrimidine-3-carbonyl]ethanesulfonamide (0.02 g, 0.03 mmol) obtained in Example 45, step 3 was dissolved in acetonitrile (1 mL) and water (0.5 mL), OXONE (0.05 mg, 0.08 mmol) was added, and the mixture was stirred at 40° C. for 1 hr. Aqueous sodium thiosulfate solution was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with water, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (chloroform/methanol=95/5) to give the title compound (0.02 g, 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729264B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-a1a84e93e84e4dcfa569cef3d3e3dc58 |
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| Source note | uspto-grants-2014_05 |
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