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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75109Generated: October 25, 2026

Ethyl Acetate → tert-Butyl 4-[2-(5-carbamoylpyrazin-2-ylamino)ethyl]piperidine-1-carboxylate

https://huagongshe.com/reaction/75109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant5-ChloropyrazinamideHCID 181450—
Reactanttert-Butyl 4-(2-aminoethyl)piperidine-1-carboxylateHCID 1514258—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Producttert-Butyl 4-[2-(5-carbamoylpyrazin-2-ylamino)ethyl]piperidine-1-carboxylateHCID 8964565079.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1.12 g (7.15 mmol) of 5-chloropyrazine-2-carboxamide, 1.95 g (8.58 mmol) of tert-butyl 4-(2-aminoethyl)piperidine-1-carboxylate and 1.18 g (8.58 mmol) of potassium carbonate in 1.4 ml of dimethyl sulphoxide is heated during 5 hours at 100° C. under an argon atmosphere and with stirring. After cooling to ambient temperature, 25 ml of ethyl acetate and 25 ml of water are added. The organic phase is separated by settling and washed 3 times with 25 ml of water and then 25 ml of a saturated aqueous sodium chloride solution. It is dried over sodium sulphate and evaporated to dryness. The residue is purified by chromatography on silica gel, elution being carried out with a 97:3, then 95:5 and 93:7 mixture of dichloromethane and methanol, in order to obtain 1.99 g (5.69 mmol) of product in the form of a light-yellow paste.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835418B2
Source datasetuspto-grants-2014_09
ORD IDord-300b12ca0b2c44e29c34b070319d84be
Source noteuspto-grants-2014_09