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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327040Generated: October 30, 2026

Piperidine → Piperiacetildenafil

https://huagongshe.com/reaction/327040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-Dihydro-5-[5-bromoacetyl)-2-ethoxyphenyl]-1-methyl-3-propyl-7H-pyrazolo[4,3-d]pyrimidin-7-oneHCID 135738550—
SolventAcetonitrileHCID 6342—
ProductPiperiacetildenafilHCID 13556475728%

Reaction Steps

Piperidine (0.22 ml, 0.0022 mol) was added to a stirred suspension of 5-(5-bromoacetyl-2-ethoxyphenyl)-1-methyl-3-n-propyl-1,6-dihydro-7H-pyrazolo [4,3-d]pyrimidin-7-one (preparation 8, 0.95 g, 0.0022 mol) and anhydrous potassium carbonate (0.6 g, 0.0044 mol) in acetonitrile (50 ml) at room temperature. After 18 hours the mixture was evaporated under vacuum, the residue dissolved in water (50 ml) and the solution extracted with ethyl acetate (3×30 ml). The organic extracts were combined, washed with brine (3×20 ml), dried (Na2SO4) and evaporated under vacuum. The resulting yellow solid was chromatographed in silica gel (12 g), using a methanol in dichloromethane elution gradient (0-2% methanol), to give an off-white solid. Crystallisation from ethyl acetate-hexane gave the title compound as an off-white powder (0.27 g, 28%), m.p. 149°-151° C. Found C,66.13; H,6.90; N,15.95. C24H31N5O5 requires C, 65.88; H,7.14; N,16.01%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05272147
Source datasetuspto-grants-1993_12
ORD IDord-efc34f77f3e04212bb2263d38319b9a1
Source noteuspto-grants-1993_12