Reaktion #65375

ord-26d7bba25a444fda9c4c5d1935446a9b

Reaktionsgleichung

COc1ccc(Cl)c(Oc2c(CCl)ncnc2NS(=O)(=O)c2ccc(C(C)(C)C)cc2)c1
4-tert-butyl-N-[6-chloromethyl-5-(2-chloro-5-methoxy-phenoxy)-pyrimidin-4-yl]-benzenesulphonamide
NCCO
ethanolamine
→
COc1ccc(Cl)c(Oc2c(CNCCO)ncnc2NS(=O)(=O)c2ccc(C(C)(C)C)cc2)c1
4-tert-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-6-(2-hydroxy-ethylaminomethyl)-pyrimidin-4yl]-benzenesulphonamide

Edukte

COc1ccc(Cl)c(Oc2c(CCl)ncnc2NS(=O)(=O)c2ccc(C(C)(C)C)cc2)c1
4-tert-butyl-N-[6-chloromethyl-5-(2-chloro-5-methoxy-phenoxy)-pyrimidin-4-yl]-benzenesulphonamide
NCCO
ethanolamine

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

By reacting 4-tert-butyl-N-[6-chloromethyl-5-(2-chloro-5-methoxy-phenoxy)-pyrimidin-4-yl]-benzenesulphonamide with ethanolamine there was obtained 4-tert-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-6-(2-hydroxy-ethylaminomethyl)-pyrimidin-4yl]-benzenesulphonamide.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05420129uspto-grants-1995_05