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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245657Generated: October 29, 2026

Triethylamine → N-((3-chloropyrazin-2-yl)methyl)-4-oxocyclohexanecarboxamide

https://huagongshe.com/reaction/245657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-OxocyclohexanecarboxylateHCID 5460131—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant(3-Chloropyrazin-2-yl)methanamine hydrochlorideHCID 42614233—
SolventDichloromethaneHCID 6344—
ProductN-((3-chloropyrazin-2-yl)methyl)-4-oxocyclohexanecarboxamideHCID 86674630104.7%

Reaction Steps

To a stirred suspension of 2-aminomethyl-3-chloropyrazine hydrochloride (3.89 mmol, 0.70 g) in dichloromethane (25 mL) at room temperature was subsequently added triethylamine (7.78 mmol, 1.08 mL), O-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluroniumhexafluorophosphate (4.67 mmol, 1.77 g) and finally 4-oxocyclohexanecarboxylate (3.89 mmol, 553 mg). After stirring for 16 hours, the suspension filtered over decalite. The decalite was washed with dichloromethane. The filtrate was washed with water, dried (sodium sulfate) and concentrated in vacuo. The resulting crude product was purified by column chromatography on silica gel (ethyl acetate). The product was dissolved in dichloromethane, washed with water and concentrated in vacuo to afford 1.09 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658794B2
Source datasetuspto-grants-2014_02
ORD IDord-aa3acf190c714b1faa396a1e1c0a9852
Source noteuspto-grants-2014_02