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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1192839Erstellt: 23. Oktober 2026

N-[(6-chloropyridin-3-yl)methyl]-2,2-difluoroethanamine → N-[(6-chloropyridin-3-yl)methyl]-N-(2,2-difluoroethyl)-4-hydroxy-2-oxo-2,5-dihydrofuran-3-carboxamide

https://huagongshe.com/de/reaction/1192839

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-[(6-chloropyridin-3-yl)methyl]-2,2-difluoroethanamineHCID 44604123—
EduktMethyl 4-hydroxy-2-oxo-2,5-dihydrofuran-3-carboxylateHCID 54677706—
LösungsmittelButyronitrileHCID 8008—
ProduktN-[(6-chloropyridin-3-yl)methyl]-N-(2,2-difluoroethyl)-4-hydroxy-2-oxo-2,5-dihydrofuran-3-carboxamideHCID 86661408—

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

10 g of methyl 4-hydroxy-2-oxo-2,5-dihydrofuran-3-carboxylate are initially introduced in 111 g of butyronitrile and admixed with 5 g of N-[(6-chloropyridin-3-yl)methyl]-2,2-difluoroethanamine. The solution is heated at 65° C. for 3 h. The solution is then extracted with 300 ml of water and then washed with 300 ml of 5% strength hydrochloric acid solution. The organic phase is dried over magnesium sulphate and the solvent is removed in vacuo. For purification, recrystallization from isopropanol is carried out.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08680285B2
Quelldatensatzuspto-grants-2014_03
ORD IDord-33b2f7e565e44cbd870ad14183a7eeae
Quellennotizuspto-grants-2014_03