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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1638989Erstellt: 25. Oktober 2026

Ethyl cysteinate hydrochloride → HCID 14600711, Verbindung

https://huagongshe.com/reaction/1638989

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl cysteinate hydrochlorideHCID 2723617—
EduktSodium ethoxideHCID 2723922—
EduktSodiumHCID 5360545—
EduktBenzyl 4-(2-iodoethyl)piperidine-1-carboxylateHCID 14600697—
LösungsmittelEthanolHCID 702—
ProduktHCID 14600711HCID 1460071192,4%

Reaktionsschritte

In a nitrogen gas flow, 8.3 g of L-cysteine ethyl ester hydrochloride is added to a sodium ethoxide solution prepared by adding 2 g of metallic sodium to 80 ml of absolute ethanol. After stirring for 1 hours at room temperature, 80 ml of an ethanol solution containing 18.4 g of 2-(1-benzyloxycarbonyl-4-piperidyl)ethyl iodide is added dropwise to this reaction mixture. After stirring for 1 hour at room temperature, the reaction liquid is concentrated under reduced pressure. To the resulting residue, ice-cold water is added. After extracting with ether, the organic layer is washed with water, and dried over magnesium sulfate. Thereafter, the solvent is distilled off under reduced pressure to give 16.3 g of oily S-[2-(1-benzyloxycarbonyl-4-piperidyl)ethyl]-L-cysteine ethyl ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04882326
Quelldatensatzuspto-grants-1989_11
ORD IDord-c92e75a3332149228b45d799ac941ab9
Quellennotizuspto-grants-1989_11