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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073021Generated: October 27, 2026

Triethylamine → HCID 15070166, compound

https://huagongshe.com/reaction/1073021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(Trifluoromethyl)anilinium chlorideHCID 2723961—
Reactant2-(4-((6-Chloro-2-quinoxalinyl)oxy)phenoxy)propanoyl chlorideHCID 13370018—
SolventAcetonitrileHCID 6342—
ProductHCID 15070166HCID 15070166—

Reaction Steps

A solution of 7.25 mmol of 2-(4-((6-chloro-2-quinoxalinyl)oxy)phenoxy)propionyl chloride, prepared using substantially the procedure of Step A of Example 1 from the corresponding acid, in 20 ml of acetonitrile was added to solution of 1.43 g (7.25 mmol) of 4-aminobenzotrifluoride, hydrochloride and 1.83 g (18.1 mmol) of triethylamine in 10 ml of acetonitrile. The reaction mixture was warmed at reflux for a period of 4 hours and then poured over crushed ice. The resulting precipitate was collected by filtration and then recrystallized from acetonitrile to give 2.40 g (68 percent of theoretical) of the above-named product as a tan solid which melted at 176°-178° C. The structure of the product was confirmed by its IR and NMR spectrum. (Compound 5)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968343
Source datasetuspto-grants-1990_11
ORD IDord-2c9e7a373d2d492894c8e89dd98de2f0
Source noteuspto-grants-1990_11