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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273574Generated: October 31, 2026

Triethylamine → HCID 50913358, compound

https://huagongshe.com/reaction/2273574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-AminopyridineHCID 10009—
ReactantThionyl ChlorideHCID 24386—
Reactant3-Cyclopropyl-1,2-oxazole-4-carboxylic acidHCID 45084772—
CatalystDimethylformamideHCID 6228—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 50913358HCID 50913358—

Reaction Conditions

Temperature65 °C

Reaction Steps

400 mg (2.6 mmol) of 3-cyclopropyl-isoxazole-4-carboxylic acid were suspended in 10 mL of toluene and one drop of dimethylformamide was added to the mixture. 0.24 mL of thionylchloride (3.3 mmol) were added at room temperature and the reaction mixture was stirred at 65° C. for two hours. After removal of the solvent, toluene was added and the evaporation was repeated. The obtained residue was then dissolved in 5 mL of dichloromethane and the solution was added dropwise to a solution containing 246 mg pyridin-3-ylamine (2.6 mmol) and 0.45 ml triethyl amine (3.3 mmol) in 5 ml dichloromethane. The mixture was stirred at room temperature for 16 h and the solvent was removed under vacuum. The residue was purified by flash column chromatography (silica, gradient elution cyclohexane→ethyl acetate→methanol) and the solvent was removed under vacuum to give 436 mg (69%, 95% purity) of the title compound as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09125414B2
Source datasetuspto-grants-2015_09
ORD IDord-f8f8674537ee42e1b1cc591479683bb9
Source noteuspto-grants-2015_09