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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1903872Erstellt: 25. Oktober 2026

Ethylmorpholine → Boc-Tyr-(D)Ala-Gly-MePhe methioninol

https://huagongshe.com/reaction/1903872

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylmorpholineHCID 7525—
EduktIsobutyl chloroformateHCID 62365—
EduktBoc-tyr-D-ala-gly-OHHCID 7272028—
EduktH-MePhe methioninolHCID 131713440—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelH-Tyr-(D)Ala-Gly-Phe methioninolHCID 131712171—
ProduktBoc-Tyr-(D)Ala-Gly-MePhe methioninolHCID 131712177—

Reaktionsschritte

1.23 g of Boc-Tyr-(D)Ala-Gly-OH is dissolved in 30 ml of THF and cooled to 15°. 0.38 ml of ethylmorpholine are added with stirring followed by 0.39 ml of chloroformic acid iso-butyl ester and stirring continued for 10 minutes. A cold solution of 14 g of TFA.H-MePhe-methioninol and 0.45 ml of N-ethylmorpholine in 12 ml of TFA are added with stirring at -15°. The mixture is stirred for 20 hours at 0°, diluted with 250 ml of acetic acid and washed repeatedly with water, 1 N citric acid, 10% KHCO3 and 30% NaCl solution. The liquid is dried over Na2SO4 and evaporated. The residue is purified chromatographically on kieselgel using a mixture of methanol/CH2Cl2 /50% acetic acid, whereby the title compound is obtained. Decomp. 160°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04438103
Quelldatensatzuspto-grants-1984_03
ORD IDord-56049c7444b54325a9f1bc890210a4f4
Quellennotizuspto-grants-1984_03