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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1155499Generated: November 2, 2026

Triethylamine → 1-(6-Chloropyrazin-2-yl)piperidin-4-one

https://huagongshe.com/reaction/1155499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
Reactant2,6-DichloropyrazineHCID 78504—
SolventAcetonitrileHCID 6342—
Product1-(6-Chloropyrazin-2-yl)piperidin-4-oneHCID 1280221571%

Reaction Conditions

Temperature10 °C

Reaction Steps

A solution of 3.0 g (20 mmol) 2,6-dichloropyrazine, 2.0 g (20 mmol) triethylamine, and 2.9 g (20 mmol) 1,4-dioxa-8-azaspiro[4.5]decane in 60 ml acetonitrile is refluxed 17 hours. The solvent is removed in vacuo, and the residue is dissolved in ethylacetate. After washing with water and brine, the organic fraction is dried (MgSO4) and evaporated to an oil. The oil is dissolved in 30 ml acetone and mixed with 30 ml 1N HCl. After heating this solution on the steam bath 30 minutes, the acetone is evaporated, and the concentrate is cooled to 10° C. A solid separates which is filtered and dried to afford 3 g (71%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04302455
Source datasetuspto-grants-1981_11
ORD IDord-6d37a1a7e98e4d088599128897cb034a
Source noteuspto-grants-1981_11