Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 647399Erstellt: 24. Oktober 2026

4-Methylmorpholine → HCID 178425962, Verbindung

https://huagongshe.com/de/reaction/647399

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
EduktAminoethylpiperazineHCID 8795—
EduktBoc-Leu-OSuHCID 11023929—
EduktHCID 178425963HCID 178425963—
KatalysatorPalladiumHCID 23938—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 178425962HCID 17842596290,1%

Reaktionsschritte

In 120 ml of dimethylformamide are dissolved 9.5 g (13 millimoles) of Z-Gln-Arg(Mts)-Leu-OH obtained according to the process of Example 20 and 5.2 g (16 millimoles) of Boc-Leu-OSu, and 1.43 ml of N-methylmorpholine is added to the solution. Then 0.5 g of 10% Pd-C is added to the mixture, and the mixture is stirred for 5 hours in a current of H2. The N-(2-aminoethyl)piperazine is added to the mixture, the mixture is stirred for 1 hour. The 10% Pd-C is recovered by filtration, and the mixture is cancentrated under reduced pressure. The residue is added to a liquid mixture of 100 ml of ethyl acetate and 200 ml of a dilute aqueous solution of citric acid. The mixture is sufficiently stirred, and the ethyl acetate layer is recovered, washed with water, dried and concentrated under reduced pressure. Ether is added to the concentrate and the precipitate is recovered by filtration to obtain 9.5 g of intended Boc-Leu-Gln-Arg(Mts)-Leu-OH (the yield being 86.5%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04407745
Quelldatensatzuspto-grants-1983_10
ORD IDord-db098f4765ef44d5a546f26b6cd99fb0
Quellennotizuspto-grants-1983_10