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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489409Generated: October 28, 2026

HCID 178471076, compound → ethyl 3-[4-(2-chlorophenyl)-5-cyano-2,4-dihydro-1H-pyrazolo[3,4-b]pyridin-6-yl]propanoate

https://huagongshe.com/reaction/489409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178471076HCID 178471076—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Productethyl 3-[4-(2-chlorophenyl)-5-cyano-2,4-dihydro-1H-pyrazolo[3,4-b]pyridin-6-yl]propanoateHCID 17847107861.2%

Reaction Steps

A suspension of 4-(2-chlorophenyl)-5-cyano-4,7-dihydro-6-(trans-2-ethoxycarbonylethenyl)-2H-pyrazolo[3,4-b]pyridine (260 mg) and 5% palladium on carbon (110 mg) in ethanol was subjected to catalytic hydrogenation at room temperature for 5 hours. The reaction mixture was filtered through Celite and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent:hexane-ethyl acetate (1:1)) to give a yellow solid. The yellow solid was crystallized from ethyl acetate-diisopropyl ether to give the title compound (160 mg) as pale-yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06977262B2
Source datasetuspto-grants-2005_12
ORD IDord-13b0b2f7300e4613b79e4751d1360db9
Source noteuspto-grants-2005_12