Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 44706Erstellt: 23. Oktober 2026

Triethylamine → 1-{[(3-Nitroquinolin-4-yl)amino]methyl}cyclobutanol

https://huagongshe.com/de/reaction/44706

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt4-Chloro-3-nitroquinolineHCID 11275808—
Edukt1-(Aminomethyl)cyclobutan-1-olHCID 28260009—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-{[(3-Nitroquinolin-4-yl)amino]methyl}cyclobutanolHCID 57457811—

Reaktionsschritte

To a solution of 1-(aminomethyl)cyclobutanol (62.5 mmol) in dichloromethane (312 mL) was added triethylamine (8.71 mL, 62.5 mmol) and 4-chloro-3-nitroquinoline (13.04 g, 62.5 mmol). More triethylamine (3 mL) was added almost immediately. The reaction was stirred under N2 for 10 d at rt, then was diluted with dichloromethane and washed with 1 M aqueous NaOH. A solid formed and was isolated by filtration. The organic layer was washed with water and brine, dried over Na2SO4, filtered, and concentrated to a solid that was crystallized from isopropanol. The resulting crystals were combined with the solid that was isolated from the extraction and the mixture was triturated with hot isopropanol. The solid was isolated by filtration, washed with diethyl ether, and air dried to yield 1-{[(3-nitroquinolin-4-yl)amino]methyl}cyclobutanol as yellow crystals. (12.83 g, 75%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541438B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-220d0047b7ff4594bc9afa7e60146efa
Quellennotizuspto-grants-2013_09