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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577766Generated: October 27, 2026

Water → 6-(cyclopentylmethyl-ethyl-amino)-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carbaldehyde

https://huagongshe.com/reaction/577766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Chloro-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carbaldehydeHCID 16228660—
ReactantN-(cyclopentylmethyl)-N-ethylamineHCID 43163716—
SolventDimethylformamideHCID 6228—
Product6-(cyclopentylmethyl-ethyl-amino)-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carbaldehydeHCID 57486804—

Reaction Steps

A suspension of 6-chloro-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carbaldehyde (5 g, 0.023 mol) and potassium carbonate (9.9 g, 0.0717 mol) in DMF (75 mL) was stirred for 20 min at RT. Cyclopentylmethyl ethyl amine (4.25 g, 33.0 mmol) was then added and the reaction was refluxed for 8 h. After cooling the reaction to RT, water (500 mL) was added to the reaction mixture and extracted with ethyl acetate (3×400 mL) and the combined organic layers were dried and concentrated. The residue was purified by silica gel (100-200 mesh) column chromatography. Elution with 10% ethyl acetate in hexanes gave the pure product as a colorless, gummy mass (76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040558B2
Source datasetuspto-grants-2015_05
ORD IDord-535836a3781a447b9c51e84b536077d9
Source noteuspto-grants-2015_05