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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026947Generated: November 2, 2026

Acetonitrile → HCID 67541052, compound

https://huagongshe.com/reaction/1026947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantSodium ThiosulfateHCID 24477—
ReactantPotassium hydroxy sulfiteHCID 23707502—
ReactantHCID 67539587HCID 67539587—
SolventWaterHCID 962—
ProductHCID 67541052HCID 6754105271%

Reaction Conditions

Temperature40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729264B2
Source datasetuspto-grants-2014_05
ORD IDord-a1a84e93e84e4dcfa569cef3d3e3dc58
Source noteuspto-grants-2014_05