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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615405Generated: November 2, 2026

Water → 3-Pyridinecarboxylic acid, 6-(4-amino-1-piperidinyl)-, ethyl ester

https://huagongshe.com/reaction/1615405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4-PiperidinamineHCID 424361—
ReactantEthyl 6-chloronicotinateHCID 2799611—
SolventDimethylformamideHCID 6228—
Product3-Pyridinecarboxylic acid, 6-(4-amino-1-piperidinyl)-, ethyl esterHCID 11402429—

Reaction Conditions

Temperature100 °C

Reaction Steps

6-chloronicotinic acid ethyl ester (4.27 g, 23 mmol) was dissolved in DMF (30 ml), and potassium carbonate (4.77 g, 35 mmol) and 4-aminopiperidine (2.76 g, 28 mmol) were added thereto, followed by stirring at 80° C. for 3 hours and at 100° C. for 1 hour. After the reaction mixture was cooled to room temperature, water was added thereto, followed by extraction with ethyl acetate. The organic layer was washed with water and saturated sodium chloride, and then dried over anhydrous sodium sulfate. After the desiccant was filtered off, the solvent was evaporated under reduced pressure, thereby obtaining 6-(4-aminopiperidin-1-yl)nicotinic acid ethyl ester (4.17 g, 73%) as a pale brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765750B2
Source datasetuspto-grants-2014_07
ORD IDord-ddb0f9dd208046abb8126469e67ec51d
Source noteuspto-grants-2014_07