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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1480Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/1480

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktPhenyl chloroformateHCID 15891—
EduktPropargylamineHCID 239041—
EduktN-(5-amino-4-chloro-2-fluorophenyl)acetamideHCID 11769584—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-(5-Acetamido-2-chloro-4-fluorophenyl)-3-(2-propynyl)ureaHCID 53873711—

Reaktionsschritte

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 reaction 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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726126
Quelldatensatzuspto-grants-1998_03
ORD IDord-5a556d937a384abda5eb0822445fcd79
Quellennotizuspto-grants-1998_03