Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2186659Erstellt: 26. Oktober 2026

1,2-Dichloroethane → (1S,2S)-2-[4-(4-methoxyphenyl)butyryl]amino-3-morpholino-1-phenyl-1-propanol

https://huagongshe.com/reaction/2186659

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
EduktTriethylamineHCID 8471—
Edukt4-(4-Methoxyphenyl)butyric acidHCID 78280—
Edukt(1S,2S)-2-amino-3-morpholino-1-phenyl-1-propanolHCID 10513992—
LösungsmittelDichloromethaneHCID 6344—
Produkt(1S,2S)-2-[4-(4-methoxyphenyl)butyryl]amino-3-morpholino-1-phenyl-1-propanolHCID 6982147866,5%

Reaktionsschritte

Methylene chloride (10 ml), 4-(4-methoxyphenyl)butanoic acid (388.0 mg, 2.0 mmol), triethylamine (0.70 ml, 5.0 mmol) and EDC (580 mg, 3.0 mmol) were added to (1S,2S)-2-amino-3-morpholino-1-phenyl-1-propanol (472.0 mg, 2.0 mmol), followed by stirring overnight. Methylene chloride (100 ml) was added to the reaction solution. After washed with a saturated sodium hydrogen carbonate solution (50 ml), water (50 ml) and saturated brine (50 ml) successively, the organic layer was dried over sodium sulfate and filtered, and the solvent was evaporated under reduced pressure. The resulting crude product was purified by silica gel column chromatography (chloroform:ethanol=20:1) to obtain the title compound (549 mg, yield 66%) as colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06407064B2
Quelldatensatzuspto-grants-2002_06
ORD IDord-b04c55622f534f38b9fb8bc490f9daf4
Quellennotizuspto-grants-2002_06