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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1279186Erstellt: 26. Oktober 2026

4-Methylmorpholine → HCID 178465172, Verbindung

https://huagongshe.com/reaction/1279186

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
Edukt1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
EduktN-HydroxysuccinimideHCID 80170—
Edukttert-Butoxycarbonyl-D-leucineHCID 637604—
EduktHCID 178465175HCID 178465175—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 178465172HCID 17846517292,1%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

H-Leu-Arg(Tos)-Pro-NHEt was dissolved in 80 mL of DMF and 200 mL of THF. With cooling the solution was neutralized with N-methylmorpholine. To the solution, a solution in which 8.86 g of Boc-D-Leu-OH and 23.02 g of HOSu were dissolved in 200 mL of THF, and 36.4 mL of WSC were added. Next the mixture was stirred at 0° C. for 5 minutes and at room temperature overnight. After confirmation with ninhidrin, the reaction mixture was concentrated under reduced pressure. To the residue, 500 mL of water was added, then the mixture was extracted 5 times with 200 mL of n-butanol and washed five times with water. The n-butanol layer was concentrated under reduced pressure, then the residue was solidified by treatment with ether. Thus 21.5 g of Boc-D-Leu-Leu-Arg(Tos)-Pro-NHEt (92.1% yield) was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06448031B1
Quelldatensatzuspto-grants-2002_09
ORD IDord-dbb7accad3824ede81c12eda69c1e149
Quellennotizuspto-grants-2002_09