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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1903869Erstellt: 25. Oktober 2026

4-Methylmorpholine → Boc-Tyr-(D)Ala-Gly-Phe methioninol

https://huagongshe.com/reaction/1903869

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
EduktEthyl chloroformateHCID 10928—
EduktBoc-tyr-D-ala-gly-OHHCID 7272028—
EduktH-Phe methioninol trifluoroacetateHCID 131712175—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktBoc-Tyr-(D)Ala-Gly-Phe methioninolHCID 131712172—

Reaktionsschritte

4.1 g of Boc-Tyr-(D)Ala-Gly-OH and 1.1 ml of N-methyl-morpholine are dissolved in 50 ml of absolute tetrahydrofuran and 1.0 ml of chloroformic acid ethyl ester added dropwise at -15°. After 5 minutes, a solution of 4.0 g of H-Phe-methioninol trifluoroacetate and 1.2 ml of N-methylmorpholine in 50 ml of DMF is added. After 1 hour's stirring at 0°, the reaction mixture is evaporated and the residue taken up in acetic acid. The solution is repeatedly washed with 10% phosphoric acid and 1 N sodium bicarbonate. After evaporation of the acetic esters, the residue is crystallised from methanol/ether. M.P. 158°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04438103
Quelldatensatzuspto-grants-1984_03
ORD IDord-e0ccf95c06124895bc341f0db4e5e91f
Quellennotizuspto-grants-1984_03