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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5396Erstellt: 24. Oktober 2026

4-Methylmorpholine → trans 3-(Acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxamide

https://huagongshe.com/de/reaction/5396

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
EduktEthyl chloroformateHCID 10928—
Edukttrans 3-(Acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxylic acidHCID 86747202—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
Produkttrans 3-(Acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxamideHCID 86747204—

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

Trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxylic acid (0.30 g, 1.05 mmol) is dissolved in tetrahydrofuran (5.0 mL). 4-Methylmorpholine (0.14 mL, 1.05 mmol) is then added, and the reaction is cooled to -20° C. Ethyl chloroformate (0.1 mL, 1.05 mmol) is then added, and the reaction is stirred at -20° C. for 30 minutes. The reaction is then filtered, and the filtrate is concentrated to give a yellow oil. This oil is dissolved in methylene chloride (20.0 mL), and anhydrous ammonia gas is bubbled through the solution for 1 hour. The bubbling is stopped, and the reaction is stirred an additional 1 hour. The solvent is evaporated, and the residue is partitioned between ethyl acetate and water. The aqueous layer is extracted several times with ethyl acetate, the combined organic layers are dried (Na2SO4), and the solvent is evaporated to give trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxamide, MS:M+1=287.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05244889
Quelldatensatzuspto-grants-1993_09
ORD IDord-6d7f78a9e4854515844933e38954e2d1
Quellennotizuspto-grants-1993_09