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HRID 434409Erstellt: 24. Oktober 2026

Hydrochloric Acid → N-[[ethoxy(4-phenylbutyl)phosphinyl]acetyl]-L-tyrosine, methyl ester

https://huagongshe.com/de/reaction/434409

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
EduktTyrosine Methyl EsterHCID 70652—
Edukt[Ethoxy(4-phenylbutyl)phosphoryl]acetic acidHCID 13136848—
LösungsmittelMethanolHCID 887—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelTriethylamineHCID 8471—
ProduktN-[[ethoxy(4-phenylbutyl)phosphinyl]acetyl]-L-tyrosine, methyl esterHCID 13171305088%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

1,1'-Carbonyldiimidazole (0.56 g) was added portionwise to a cooled (0° C.) solution of [ethoxy(4-phenylbutyl)phosphinyl]acetic acid (0.98 g) in 70 ml of acetonitrile. This reaction mixture was stirred under argon at 0° C. for 1.5 hours. The HCl salt of L-tyrosine methyl ester (0.8 g) was dissolved in methanol and neutralized with triethylamine (0.35 g). This solution was concentrated in vacuo, dissolved in 10 ml of warm acetonitrile and added dropwise to the above solution of activated phosphinic acid ester sidechain. The reaction was stirred overnight under argon and then concentrated in vacuo. A solution of the pot residue in dichloromethane was washed (H2O, aqueous NaHCO3, brine), dried (MgSO4) and filtered to yield 1.4 g of N-[[ethoxy(4-phenylbutyl)phosphinyl]acetyl]-L-tyrosine, methyl ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04396772
Quelldatensatzuspto-grants-1983_08
ORD IDord-37fd470cc21344d8ba7464aa0b158bd6
Quellennotizuspto-grants-1983_08