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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334550Generated: October 30, 2026

Trifluoroacetic acid → N-(4-Fluorophenyl)-5-(2-pyridinyl)-4-pentynamide

https://huagongshe.com/reaction/334550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 66598279HCID 66598279—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-(4-Fluorophenyl)-5-(2-pyridinyl)-4-pentynamideHCID 1161596183.3%

Reaction Steps

tert-Butyl-5-(pyridin-2-yl)pent-4-ynoyl-4-fluorophenylcarbamate (299 mg, 0.81 mmol) was dissolved in DCM (4 mL) with 0.01% w/w of water. 4 mL of trifluoroacetic acid was added at room temperature to the solution. The resulting mixture was stirred at R.T. for 2 h. The solvent was removed under reduced pressure. The brown oil was dissolved in saturated NaHCO3 until pH=8. The aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over MgSO4 and the solvent was removed under reduced pressure. The brownish solid was triturated in a mixture Et2O/Pentane: 50/50. The solid was collected by filtration and washed with a mixture Et2O/Pentane: 50/50. The solid was dried by lyophilisation to afford 181 mg of N-(4-fluorophenyl)-5-(pyridine-2-yl)pent-4-ynamide (Yield: 83%) as a colorless solid (M.P.=189.9-190.2° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883826B2
Source datasetuspto-grants-2014_11
ORD IDord-441218fe86e74590922fe418f69562d1
Source noteuspto-grants-2014_11