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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854073Generated: October 30, 2026

Sodium Hydroxide → HCID 68295077, compound

https://huagongshe.com/reaction/1854073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantPyBOPHCID 2724699—
Reactant3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridin-2-oneHCID 7063844—
ReactantHCID 68351184HCID 68351184—
SolventDimethyl SulfoxideHCID 679—
SolventEthanolHCID 702—
ProductHCID 68295077HCID 6829507750%

Reaction Conditions

Temperature60 °C

Reaction Steps

Aqueous NaOH (0.065 g, 1.634 mmol) was added to a solution of ethyl 6-(1-(tert-butoxycarbonyl)piperidin-4-yl)-1-isopropyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylate (0.34 g, 0.817 mmol) in EtOH (4 mL) and stirred at 60° C. for 1 h. After completion of the reaction, ethanol was removed under reduced pressure and it was acidified using 10% citric acid solution. Extraction was carried out using ethyl acetate; the combined organic layers were washed with water, brine and dried over anhydrous Na2SO4; filtered and concentrated under reduced pressure. The crude acid (0.3 g, 0.773 mmol) was then dissolved in DMSO (3 mL) and 3-(aminomethyl)-4,6-dimethylpyridin-2(1H)-one (0.235 g, 1.546 mmol) was added to it. The reaction mixture was stirred at room temperature for 15 min before PYBOP (0.603 g, 1.159 mmol) was added to it and stirring was continued overnight. After completion of the reaction, reaction mass was poured into ice to obtain solid, which was filtered and washed with acetonitrile followed by ether to provide the desired intermediate (0.2 g, 50.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962620B2
Source datasetuspto-grants-2015_02
ORD IDord-bcf8461f09e14572a0696a6c14b9cb3b
Source noteuspto-grants-2015_02