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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 419282Erstellt: 26. Oktober 2026

Hydroxylamine → Benzyloxy-3-nitro[1,5]naphthyridin-4-amine

https://huagongshe.com/reaction/419282

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydroxylamineHCID 787—
EduktBenzyloxy-4-chloro-3-nitroquinolineHCID 21075762—
EduktBenzyloxy-4-chloro-3-nitro[1,5]naphthyridineHCID 66650176—
ProduktBenzyloxy-3-nitro[1,5]naphthyridin-4-amineHCID 66649873—
ProduktBenzyloxy-3-nitroquinolin-4-amineHCID 66649911—

Reaktionsschritte

In step (5) of Reaction Scheme I, a benzyloxy-4-chloro-3-nitroquinoline or benzyloxy-4-chloro-3-nitro[1,5]naphthyridine of Formula XIX is treated with an amino alcohol of formula HO—(CH2)c—CH2—NH2 to provide a benzyloxy-3-nitroquinolin-4-amine or benzyloxy-3-nitro[1,5]naphthyridin-4-amine of Formula XX. The reaction is conveniently carried out by adding the amino alcohol of formula HO—(CH2)c—CH2—NH2 to a solution of a compound of Formula XIX in a suitable solvent such as dichloromethane in the presence of a tertiary amine such as triethylamine. The reaction can be carried out at ambient temperature or at an elevated temperature such as, for example, the reflux temperature of the solvent. The reaction product can be isolated using conventional methods.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08093390B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-8e73153255434929bf0f88c1d544d9d9
Quellennotizuspto-grants-2012_01