Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2394321Erstellt: 23. Oktober 2026

Water → N1-[2-(4-cyanophenoxy)-1-methylethyl]-N2-phenoxycarbonyl-L-valinamide

https://huagongshe.com/de/reaction/2394321

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt4-MethylmorpholineHCID 7972—
Edukt3-Methoxyphenyl carbonochloridateHCID 22019180—
EduktN1-[2-(4-cyanophenoxy)-1-methylethyl]L-valinamide hydrochlorideHCID 22866849—
LösungsmittelDichloromethaneHCID 6344—
ProduktN1-[2-(4-cyanophenoxy)-1-methylethyl]-N2-phenoxycarbonyl-L-valinamideHCID 5371342013,1%

Reaktionsschritte

1.0 g of N-methylmorpholine was added to a solution containing 1.5 g of N1 -[2-(4-cyanophenoxy)-1-methylethyl]-L-valinamide hydrochloride dissolved in 100 ml of methylene chloride, at -20° C. After 0.9 g of 3-methoxyphenyl chloroformate was added to the mixture at -20° C., the reaction mixture was allowed to sit and warm naturally to room temperature while being stirred. The whole mixture was stirred for 2 hours at room temperature. Water was subsequently added to the reaction mixture. After the methylene chloride layer was washed with water, the organic layer was dried over anhydrous magnesium sulfate and the methylene chloride was removed under reduced pressure. The residue was purified by column chromatography on silica gel, thus yielding 0.25 g of the desired product in the form of a white plated crystal (yield: 12%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05811424
Quelldatensatzuspto-grants-1998_09
ORD IDord-a8975b2b51594056ad5e9bacda32a3b1
Quellennotizuspto-grants-1998_09