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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1194615Erstellt: 25. Oktober 2026

Triethylamine → N-(Morpholinocarbonyl)-L-phenylalanine S-methyl-L-cysteine methyl ester

https://huagongshe.com/reaction/1194615

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktCP 84364HCID 664657—
EduktMethyl (2R)-2-amino-3-(methylsulfanyl)propanoateHCID 1277655—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelEthyl AcetateHCID 8857—
ProduktN-(Morpholinocarbonyl)-L-phenylalanine S-methyl-L-cysteine methyl esterHCID 6786590578%

Reaktionsschritte

To a solution of 0.96 g N-(morpholinocarbonyl)-L-phenylalanine 3 and 0.55 g S-methyl-L-cysteine methyl ester in 50 mL anhydrous methylene chloride at ambient temperature was added 0.50 mL triethylamine, 0.51 g 1-hydroxybenzotrazole and 0.70 g 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide hydrochloride. After being stirred for 4 h, the solution was diluted with 100 mL ethyl acetate and was washed with 2×35 mL 0.1N hydrochloric acid solution and 2×35 mL 0.1N sodium hydroxide solution. The organic phase was dried over magnesium sulfate, filtered and concentrated in vacuo to afford 1.15 g of the desired solid dipeptide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04814342
Quelldatensatzuspto-grants-1989_03
ORD IDord-f7dd55f03cf84449a8fb4ff2a54d0efc
Quellennotizuspto-grants-1989_03