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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570129Generated: October 25, 2026

Potassium Carbonate → 6-(4-Fluorophenyl)-2,3-dimethyl-2,3-dihydropyrazolo[5,1-b][1,3]oxazole

https://huagongshe.com/reaction/570129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-Butanediol, dimethanesulfonateHCID 99909—
Reactant3-(4-fluorophenyl)-1H-pyrazol-5-olHCID 178515624—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product6-(4-Fluorophenyl)-2,3-dimethyl-2,3-dihydropyrazolo[5,1-b][1,3]oxazoleHCID 8948831271.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 3-(4-fluorophenyl)-1H-pyrazol-5-ol (3 g, 16.8 mmol) in DMF (15 mL) was added K2CO3 (9.3 g, 67.4 mmol) and butane-2,3-diyl dimethanesulfonate (4.8 g, 18.5 mmol) (prepared as described in US2010/41748) at room temperature and then stirred for 16 h at 60° C. Thereafter, the reaction mixture was diluted with cold water and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulphate and concentrated to get the crude product. Purification by column chromatography over silica gel (eluent 5-10% ethyl acetate in petrol ether) yielded 6-(4-fluorophenyl)-2,3-dimethyl-2,3-dihydropyrazolo[5,1-b][1,3]oxazole (2.8 g, 71%) as yellow oil and a mixture of diastereoisomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023844B2
Source datasetuspto-grants-2015_05
ORD IDord-5fdc646e557142ff9c0d88ee8192ca33
Source noteuspto-grants-2015_05