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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783311Generated: October 30, 2026

Water → HCID 135474306, compound

https://huagongshe.com/reaction/1783311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPiperidineHCID 8082—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 23084607HCID 23084607—
SolventAcetonitrileHCID 6342—
ProductHCID 135474306HCID 135474306—

Reaction Steps

After the completion of the reaction, the reaction solution was allowed to cool to room temperature, and the precipitated solid was removed by filtration. The filtrate was concentrated, and the residue was filtrated using silica gel (hexane:ethyl acetate=2:1). The filtrate was concentrated to give 1-bromomethyl-7-fluoro-5-methoxymethoxy-3-methyl-3H-pyrazolo[3,4-c]isoquinoline (0.50 g) as crude crystals. The crude crystals (0.50 g) of 1-bromomethyl-7-fluoro-5-methoxymethoxy-3-methyl-3H-pyrazolo[3,4-c]isoquinoline, piperidine (0.30 g) and potassium carbonate (0.39 g) were dissolved in acetonitrile (20 mL), and the reaction solution was stirred at room temperature for 2 days. After the completion of the reaction, the reaction solution was poured into water and extracted with chloroform. The organic layer was dried over magnesium sulfate, and the solvent was evaporated. The residue was purified by silica gel chromatography (hexane:ethyl acetate=10:1) to give 7-fluoro-3-methyl-1-(pyrrolidin-1-ylmethyl)-3H-pyrazolo[3,4-c]isoquinolin-5(4H)-one (0.079 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501412B2
Source datasetuspto-grants-2009_03
ORD IDord-b3ca704589bc463f87fa7c77d7e5fcbd
Source noteuspto-grants-2009_03