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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 840528Erstellt: 24. Oktober 2026

Methyl iodide → HCID 22610929, Verbindung

https://huagongshe.com/de/reaction/840528

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktSodium hydrideHCID 24758—
EduktEthyl 3-amino-4,4,4-trifluoro-2-butenoateHCID 136209—
Edukt2-Ethoxycarbonylamino-3-fluoro-5-chloropyridineHCID 22610930—
EduktHCID 178418361HCID 178418361—
Lösungsmittel1-MethylpyrrolidineHCID 8454—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 22610929HCID 22610929—

Reaktionsschritte

Under a nitrogen atmosphere, while cooling and stirring, a solution of 22.7 g 4,4,4-trifluoro-3-amino-2-butenoic acid ethyl ester is added dropwise to 5.1 g of a sodium hydride dispersion (60%) in 60 ml N-methylpyrrolidine at 0-5° C. and stirred at 22° C. until hydrogen evolution is complete. Then 23.7 g 2-ethoxicarbonylamino-3-fluoro-5-chloropyridine (Example H1) is added and the reaction mixture heated for about 5 hours to 120° C. The mixture is then cooled, 16.7 g methyl iodide is added dropwise and stirring is continued overnight at 22° C. After the reaction mixture has been taken up in ethyl acetate, it is washed with ice water, dried over sodium sulfate, filtered, and concentrated by evaporation. The residue obtained is recrystallized from ethyl acetate/n-hexane. The title compound is obtained with a melting point of 133-134° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06369002B1
Quelldatensatzuspto-grants-2002_04
ORD IDord-3dfbdfd7f56740fe8ffc76e0afe2a60c
Quellennotizuspto-grants-2002_04