Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 580454Erstellt: 26. Oktober 2026

Diisopropyl Ether → 2-Amino-7-(2-morpholinoethoxy)-1,8-naphthyridine

https://huagongshe.com/reaction/580454

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropyl EtherHCID 7914—
EduktPotassium HydroxideHCID 14797—
Edukt7-Chloro-1,8-naphthyridin-2-amineHCID 85199—
Edukt1-MorpholinoethanolHCID 3029376—
KatalysatorEthanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]-HCID 112414—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelChlorobenzeneHCID 7964—
Produkt2-Amino-7-(2-morpholinoethoxy)-1,8-naphthyridineHCID 13983449—

Reaktionsschritte

Tris(3,6-dioxaheptyl)amine (1.47 g), pulverized potassium hydroxide (80% pure, 6.75 g) and morpholinoethanol (12 g) are added to a suspension of 2-amino-7-chloro-1,8-naphthyridine (16.2 g) in chlorobenzene (450 cc). The mixture is brought to 120° C. and maintained at this temperature for 3 hours. The suspension obtained after cooling is separated by filtration. The separated product is washed with chlorobenzene (3×50 cc) and water (3×50 cc). The solid obtained is redissolved in methylene chloride (400 cc). The insoluble material which remains is removed by filtration. The filtrate is dried over magnesium sulphate and concentrated to dryness at 40° C. under reduced pressure (4 kPa). The crude product obtained (23.5 g; m.p. 164° C.) is stirred in the presence of isopropyl ether (100 cc), filtered and dried at 30° C. under reduced pressure (0.07 kPa). 2-Amino-7-(2-morpholinoethoxy)-1,8-naphthyridine (13.9 g), m.p. 164° C., is obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04753933
Quelldatensatzuspto-grants-1988_06
ORD IDord-dbfe5bddf81c406cbadf904a890272a0
Quellennotizuspto-grants-1988_06