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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022730Generated: November 1, 2026

Triethylamine → 3-[(6R,7S)-7-(3,4-dichlorophenyl)-1,4-oxazepan-6-yl]imidazolidine-2,4-dione monohydrochloride

https://huagongshe.com/reaction/1022730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl isocyanatoacetateHCID 76283—
Reactanttert-butyl (6R,7S)-6-amino-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylateHCID 66975508—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product3-[(6R,7S)-7-(3,4-dichlorophenyl)-1,4-oxazepan-6-yl]imidazolidine-2,4-dione monohydrochlorideHCID 66976155—

Reaction Steps

To a solution of tert-butyl (6R,7S)-6-amino-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylate (100 mg) in THF (3 mL) were added triethylamine (0.058 ml) and ethyl isocyanatoacetate (0.047 mL) at room temperature, and the mixture was stirred at room temperature overnight. The reaction mixture was diluted with ethyl acetate. The diluted solution was washed with distilled water and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, 2.0 M hydrogen chloride-ethanol solution (8 mL) was added to the obtained residue at room temperature, and the mixture was stirred at 80° C. for 3 weeks. The residue obtained by concentration under reduced pressure was washed with diethyl ether to give the title compound (89 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722662B2
Source datasetuspto-grants-2014_05
ORD IDord-4ac44ee4f40b4853a598afe7c3d4cd19
Source noteuspto-grants-2014_05