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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 233373Erstellt: 25. Oktober 2026

benzyl (2S)-2-aminopropanoate → N-(2-acetylthiomethyl-1-oxo-3-phenylbutyl)alanine benzyl ester

https://huagongshe.com/reaction/233373

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktbenzyl (2S)-2-aminopropanoateHCID 726858—
Edukt2-Acetylthiomethyl-3-phenylbutanoic acidHCID 10060778—
ProduktN-(2-acetylthiomethyl-1-oxo-3-phenylbutyl)alanine benzyl esterHCID 1040950368%

Reaktionsschritte

Using the procedure described in Example 60, starting with 2-acetylthiomethyl-3-phenylbutanoic acid and alanine benzyl ester, and after purification by chromatography, eluting with a cyclohexane/ethyl acetate (75:25 by volume) mixture, N-(2-acetylthiomethyl-1-oxo-3-phenylbutyl)alanine benzyl ester is obtained in a 68% yield, the characteristics of which are as follows: Rf =0.31 [hexane/ethyl acetate (75:25 by volume)].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05591891
Quelldatensatzuspto-grants-1997_01
ORD IDord-9b5dcb10338a4a08b8c4c2a7531a5a67
Quellennotizuspto-grants-1997_01