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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 848727Erstellt: 25. Oktober 2026

Sodium Iodide → 2-(2-carbamoyl-5-chlorophenylamino)-N-(3,4-dimethoxyphenethyl)acetamide

https://huagongshe.com/reaction/848727

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
Edukt2-Chloro-N-(2-(3,4-dimethoxy-phenyl)-ethyl)-acetamideHCID 26622—
EduktMagnesium monoxideHCID 6850729—
Edukt2-Amino-4-chlorobenzamideHCID 12374837—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(2-carbamoyl-5-chlorophenylamino)-N-(3,4-dimethoxyphenethyl)acetamideHCID 1009188168,2%

Reaktionsschritte

To a mixture of 7.73 g of 2-chloro-N-(3,4-dimetoxyphenethyl)acetamide, 5.12 g of 2-amino-4-chlorobenzamide, 13.5 g of sodium iodide and 3.63 g of magnesium oxide was added 30 ml of dimethylformamide and the resulting mixture was stirred at 90° to 100° C. for 4.5 hours. The reaction solution was concentrated under reduced pressure and the residue was extracted with 500 ml of chloroform. The chloroform extract was washed successively with 10% hydrochloric acid, water, a 5% aqueous sodium carbonate solution, a 5% aqueous sodium sulfite solution and water, dried and then concentrated to dryness under reduced pressure. The residue was recrystallized from methanol to obtain 8.01 g of 2-(2-carbamoyl-5-chlorophenylamino)-N-(3,4-dimethoxyphenethyl)acetamide having a melting point of 167.5°-168.5° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04297357
Quelldatensatzuspto-grants-1981_10
ORD IDord-1b4f0eca18164eb1a151fd9e5085d218
Quellennotizuspto-grants-1981_10