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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333979Generated: October 29, 2026

Hydrochloric Acid → N-Methyl-4-piperazin-1-yl-pyridine-2-carboxamide hydrochloride

https://huagongshe.com/reaction/333979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPiperazineHCID 4837—
Reactant1,4-DioxaneHCID 31275—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Chloro-N-methylpicolinamideHCID 1476814—
Solvent1-ButanolHCID 263—
SolventEthanolHCID 702—
ProductN-Methyl-4-piperazin-1-yl-pyridine-2-carboxamide hydrochlorideHCID 6683594833.2%

Reaction Steps

A mixture of 4-Chloro-N-methyl-pyridine-2-carboxamide (400 mg, 2.345 mmol), piperazine (808 mg, 9.38 mmol) and sodium bicarbonate (591 mg, 7.03 mmol) in 1-butanol (4 ml) was heated under reflux for 18 hours. The mixture was filtered, the filtrate was concentrated under reduced pressure and the residue was purified by column chromatography (silica, 1-5% MeOH—basified with ammonia—in DCM) to give a colourless oil. The oil was dissolved in 2 ml ethanol and 4N HCl in dioxane (1.11 ml, 4.4 mmol) was added. The mixture was stirred for 1 hour at room temperature and filtered. The filter residue was rinsed with DCM and ethanol, dried under reduced pressure to give 200 mg of a white solid (0.779 mmol, 33%). MS (ESI) m/z=221.2 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883791B2
Source datasetuspto-grants-2014_11
ORD IDord-e94cb864eb404ae4a129d9471dbda4ba
Source noteuspto-grants-2014_11