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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693562Generated: November 4, 2026

6-[4-(2-Butoxy-vinyl)-phenyl]-5-(4-chloro-phenyl)-1-phenyl-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-one → 6-[4-(2-Butoxyethyl)-phenyl]-5-(4-chloro-phenyl)-1-phenyl-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-one

https://huagongshe.com/reaction/1693562

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-[4-(2-Butoxy-vinyl)-phenyl]-5-(4-chloro-phenyl)-1-phenyl-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-oneHCID 67281469—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product6-[4-(2-Butoxyethyl)-phenyl]-5-(4-chloro-phenyl)-1-phenyl-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-oneHCID 5789802270.1%

Reaction Steps

To a solution of 6-[4-(2-butoxy-vinyl)-phenyl]-5-(4-chloro-phenyl)-1-phenyl-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-one (5 mg, 0.01 mmol) in EtOH (1 mL) is added Pd/C (2 mg). The system is degassed by alternately applying vacuum and H2 for 3 times. The mixture is then stirred at room temperature under H2 for 24 h. After removing the catalyst by filtration, the filtrate is concentrated and purified by flash column chromatography (silica gel, 0˜30% EtOAc/hexane) to provide the title compound as white solid (3.5 mg, 69%). HPLC-MS calculated C29H25ClN4O2 (M+1+): 497.2. Found: 497.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158634B2
Source datasetuspto-grants-2012_04
ORD IDord-de6936af252949f9b6c5abbce84fd2da
Source noteuspto-grants-2012_04