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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926111Generated: November 1, 2026

Dimethylformamide → 2-{2-[7-(methylthio)-1H-pyrazolo[4,3-d]pyrimidin-1-yl]ethoxy}ethyl benzoate

https://huagongshe.com/reaction/1926111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant7-(methylthio)-1H-pyrazolo[4,3-d]pyrimidineHCID 55295894—
Reactant2-{2-[(Methylsulfonyl)oxy]ethoxy}ethyl benzoateHCID 86615775—
SolventWaterHCID 962—
Product2-{2-[7-(methylthio)-1H-pyrazolo[4,3-d]pyrimidin-1-yl]ethoxy}ethyl benzoateHCID 6752085033.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 7-(methylthio)-1H-pyrazolo[4,3-d]pyrimidine (747 mg), 2-{2-[(methylsulfonyl)oxy]ethoxy}ethyl benzoate (1.43 g), potassium carbonate (931 mg) and N,N-dimethylformamide (12 mL) was stirred at 60° C. for 4 hrs. The reaction mixture was poured into water (30 mL), and the mixture was extracted with ethyl acetate (50 mL×2). The organic layers were combined, washed with saturated brine and dried over anhydrous magnesium sulfate. After concentration under reduced pressure, the residue was purified by silica gel column chromatography (eluent, hexane:ethyl acetate=80:20→20:80), and further purified by basic silica gel column chromatography (eluent, hexane:ethyl acetate=90:10→40:60) to give the title compound (533 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178543B2
Source datasetuspto-grants-2012_05
ORD IDord-a990ffbe4e2d43da8d5a3f212ff70cf5
Source noteuspto-grants-2012_05