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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22664Generated: October 26, 2026

Methanol → 2-(4-fluorophenyl)-3-(2-methanesulfonyl-pyrimidin-4-yl)-6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-1-one

https://huagongshe.com/reaction/22664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium peroxymonosulphateHCID 10313463—
Reactant2-(4-fluorophenyl)-3-(2-methylsulfanyl-pyrimidin-4-yl)-6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-1-oneHCID 12991404—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventSodium BicarbonateHCID 516892—
Product2-(4-fluorophenyl)-3-(2-methanesulfonyl-pyrimidin-4-yl)-6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-1-oneHCID 12991405—

Reaction Steps

To a solution of 2-(4-fluorophenyl)-3-(2-methylsulfanyl-pyrimidin-4-yl)-6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-1-one, 4, (1.3 g. 3.8 mmol) in THF: methanol (56 mL of a 1:1 mixture) is added dropwise a solution of Oxone® (potassium peroxymonosulfate) (9.34 g, 15.2 mmol) in water (42 mL). The reaction is stirred 1 hour at room temperature, diluted with aqueous NaHCO3 and extract three times with ethyl acetate. The organic layers are combined, dried, and concentrated in vacuo too afford the crude desired product which is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849627B2
Source datasetuspto-grants-2005_02
ORD IDord-3c4a936328eb405499a9954e76af0c30
Source noteuspto-grants-2005_02