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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182895Generated: November 1, 2026

Triethylamine → HCID 178461109, compound

https://huagongshe.com/reaction/1182895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-(1-Fluoroethyl)-6,7-dichloro-[1,2,4]triazolo[1,5-a]pyrimidineHCID 86036549—
ReactantHCID 178445676HCID 178445676—
CatalystTetrabutylammonium IodideHCID 67553—
SolventTolueneHCID 1140—
ProductHCID 178461109HCID 178461109—

Reaction Steps

0.220 g (2.2 mmol) Triethylamine, a spatula tip of tetrabutylammonium iodide and 0.340 g (2.2 mmol) of cis-4-tert-butylcyclohexylamine were added successively to a solution of 0.470 g (2.0 mmol) of 5-(1-fluoroethyl)-6,7-dichloro-[1,2,4]triazolo[1,5-a]pyrimidine in 15 ml of toluene under stirring. The reaction mixture was heated at reflux for 5 hours and then stirred for another 12 hours at room temperature. The solvent was evaporated under reduced pressure and dichloromethane was added to the resulting residue. The resulting reaction mixture was washed with 2N hydrochloric acid and water. The organic phase was separated, dried and the solvent was evaporated under reduced pressure. Treatment of the resulting residue with hexane yielded 0.540 g (1.5 mmol, 76% of theory) of the title compound having a melting point of 138-139° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664235B2
Source datasetuspto-grants-2014_03
ORD IDord-b3856b4e115446bdb110b713d9e0fb18
Source noteuspto-grants-2014_03