Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 540802Erstellt: 24. Oktober 2026

Ammonium Hydroxide → Oxane-4-carboxamide

https://huagongshe.com/de/reaction/540802

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium HydroxideHCID 14923—
Edukt2H-Pyran-4-carboxylic acid, tetrahydro-, methyl esterHCID 2773520—
EduktBenzyloxy-4-chloro-3-nitroquinolineHCID 21075762—
EduktBenzyloxy-3-nitroquinolin-4-amineHCID 66649911—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTriethylamineHCID 8471—
ProduktOxane-4-carboxamideHCID 13197203—

Reaktionsschritte

In step (5) of Reaction Scheme I, a benzyloxy-4-chloro-3-nitroquinoline of Formula XIX is treated with an amine of Formula R1—NH2 to provide a benzyloxy-3-nitroquinolin-4-amine of Formula XX. The reaction is conveniently carried out by adding the amine of Formula R1—NH2 to a solution of the benzyloxy-4-chloro-3-nitroquinoline of Formula XIX in a suitable solvent such as dichloromethane or methanol 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. Several mines of Formula R1—NH2 are commercially available; others can be prepared by known synthetic methods. For example, methyl tetrahydro-2H-pyran-4-carboxylate treated with ammonium hydroxide to form tetrahydro-2H-pyran-4-carboxamide, which can then be reduced with lithium aluminum hydride to provide tetrahydro-2H-pyran-4-ylmethylamine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08871782B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-ce9fce475629448ab676fa3dcd87db44
Quellennotizuspto-grants-2014_10