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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643047Generated: October 30, 2026

Triethylamine → HCID 11449562, compound

https://huagongshe.com/reaction/643047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-FluoroethylamineHCID 9996—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant3-(5-Dimethylcarbamoyl-pent-1-ynyl)-benzoic acidHCID 11482335—
SolventDichloromethaneHCID 6344—
ProductHCID 11449562HCID 1144956291%

Reaction Steps

To a solution of 3-(5-dimethylcarbamoyl-pent-1-ynyl)-benzoic acid (0.100 g, 0.38 mmol) in dry dichloromethane (1.5 mL) under a nitrogen atmosphere at room temperature, EDCI (0.0728 g, 0.38 mmol) was added followed by triethylamine (0.162 mL, 1.14 mmol), the resulting mixture was stirred at room temperature for further 5 minutes. 2-Fluoro ethylamine (0.189 g, 1.9 mmol) was then added and the mixture stirred at room temperature for 16 hrs. The reaction mixture was washed with a mixture of saturated brine and saturated sodium bicarbonate (1:1; 2×150 mL) followed by saturated brine solution (100 mL). The organic layer was separated and dried over magnesium sulfate and the solvent evaporated under vacuum. The residue was purified by flash column chromatography on silica gel (DCM:MeOH, 95% to 5% methanol gradient) to afford 3-(5-dimethylcarbamoyl-pent-1-ynyl)-N-(2-fluoro-ethyl)benzamide (26)(0.103 g, 0.34 mmol, 91% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696382B2
Source datasetuspto-grants-2010_04
ORD IDord-b8dda3fd4f2f4b63a69c7c49bfb71375
Source noteuspto-grants-2010_04