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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976974Generated: October 29, 2026

Triethylamine → 1-(5-Acetamido-2-chloro-4-fluorophenyl)-3-(2-propynyl)urea

https://huagongshe.com/reaction/976974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenyl chloroformateHCID 15891—
ReactantPropargylamineHCID 239041—
ReactantN-(5-amino-4-chloro-2-fluorophenyl)acetamideHCID 11769584—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1-(5-Acetamido-2-chloro-4-fluorophenyl)-3-(2-propynyl)ureaHCID 53873711—

Reaction Steps

A solution of 5'-amino-4'-chloro-2'-fluoroacetanilide (11.25 g, 55.6 mmol), and triethylamine (7.70 mL, 55.6 mmol) in tetrahydrofuran is added dropwise to a stirred solution of phenylchloroformate (8.70 mL, 69.4 mmol) in tetrahydrofuran while maintaining the reaction mixture temperature at 25°-30° C. After the addition is complete, the rection mixture is stirred at room temperature for 75 minutes, and poured into ethyl acetate. The organic mixture is washed sequentially with water, saturated sodium hydrogen carbonate solution and brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo to obtain a tan solid. A solution of the solid in tetrahydrofuran is treated with propargylamine (9.52 mL, 139 mmol), refluxed for 1 hour, and poured into water. The aqueous mixture is filtered to obtain a solid which is washed sequentially with water, 0.5N hydrochloric acid and water, and dried overnight to give the title product as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05612481
Source datasetuspto-grants-1997_03
ORD IDord-6e164b38933b4bb8a4e014101cd34a9a
Source noteuspto-grants-1997_03