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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516189Generated: October 30, 2026

Ethyl Acetate → HCID 89870901, compound

https://huagongshe.com/reaction/516189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantTert-butyl (3R)-3-(methanesulfonyloxy)pyrrolidine-1-carboxylateHCID 10934372—
ReactantHCID 178508725HCID 178508725—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 89870901HCID 89870901—

Reaction Conditions

Temperature85 °C

Reaction Steps

A suspension of 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine (446 mg), (R)-tert-butyl 3-(methylsulfonyloxy)pyrrolidine-1-carboxylate (450 mg), potassium carbonate (692 mg) in DMF (5.0 ml) was stirred at 85° C. for 6 hours. Ethyl acetate and water were added thereto to separate the organic layer. The organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The resulting residue was purified by basic silica gel column chromatography (developing solvent: hexane/ethyl acetate) to obtain the title compound as a light-yellow, amorphous substance (354 mg). Physical properties: m/z [M+H]+ 431.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108973B2
Source datasetuspto-grants-2015_08
ORD IDord-d022aebc7ccd4e8c852dfffd0cb1ebc3
Source noteuspto-grants-2015_08