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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490890Generated: October 27, 2026

Ethanol → Ethyl 4-ethoxy-1-ethyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylate

https://huagongshe.com/reaction/490890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodiumHCID 5360545—
Reactantethyl 4-chloro-1-ethyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylateHCID 10491120—
ProductEthyl 4-ethoxy-1-ethyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylateHCID 13072976—

Reaction Steps

Sodium (0.55 g, 23.7 mmol) was added portionwise to anhydrous ethanol (25 ml) at 20° C. under an atmosphere of nitrogen. After stirring for 1 hour the solution was added to Intermediate 1 (4.622 g, 18.22 mmol) and the reaction mixture heated at reflux for 2 hours. The mixture was evaporated in vacuo and the residue partitioned between dichloromethane and water. The organic phase was washed with brine, dried (Na2SO4) and evaporated in vacuo. The residue was purified on SPE cartridges (silica, 4×20 g) eluting with dichloromethane, ethyl acetate:petroleum ether (1:4, 1:2 then 1:1) followed by ethyl acetate). Appropriate fractions were combined and evaporated in vacuo to afford Intermediate 35 as white solid (4.33 g). LCMS showed MH+=264, TRET=2.77 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528148B2
Source datasetuspto-grants-2009_05
ORD IDord-af0ff26590244ea78297c1316267f1e6
Source noteuspto-grants-2009_05