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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1163909Erstellt: 24. Oktober 2026

N-Ethyltryptamine → N-ethyl-N-(N-benzyloxycarbonylglycyl)-tryptamine

https://huagongshe.com/de/reaction/1163909

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-EthyltryptamineHCID 6092—
EduktTriethylamineHCID 8471—
EduktBenzyloxycarbonylglycineHCID 14349—
EduktIsobutyl chloroformateHCID 62365—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-ethyl-N-(N-benzyloxycarbonylglycyl)-tryptamineHCID 20513176101,6%

Reaktionsbedingungen

Temperatur-15 °C

Reaktionsschritte

30 ml of anhydrous tetrahydrofuran and 1.05 g of triethylamine are added to 2.17 g of N-benzyloxycarbonyl-glycine, and 1.43 g of isobutyl chloroformate are added dropwise thereto at -15° C. under stirring. A solution of 1.96 g of N-ethyl-tryptamin (i.e., 3-(2-ethylamino)ethylindole) in 40 ml of anhydrous tetrahydrofuran is added dropwise to the mixture at the same temperature, and said mixture is stirred at 0° C. for one hour and further stirred at room temperature for 16 hours. After the reaction, the reaction mixture is evaporated to remove solvent. The residue (oil) is purified by silica gel chromatography (Solvent: ethyl acetate-chloroform (1:1). 4.0 g of N-ethyl-N-(N-benzyloxycarbonylglycyl)-tryptamine are thereby obtained as a colorless oil. Yield: 100%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04367230
Quelldatensatzuspto-grants-1983_01
ORD IDord-c07ad14976464c3099faf93d61d2dd8f
Quellennotizuspto-grants-1983_01