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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5396Generated: October 25, 2026

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

https://huagongshe.com/reaction/5396

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantEthyl chloroformateHCID 10928—
Reactanttrans 3-(Acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxylic acidHCID 86747202—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Producttrans 3-(Acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxamideHCID 86747204—

Reaction Conditions

Temperature-20 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244889
Source datasetuspto-grants-1993_09
ORD IDord-6d7f78a9e4854515844933e38954e2d1
Source noteuspto-grants-1993_09