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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362888Generated: November 1, 2026

Chloroacetamide → HCID 58046811, compound

https://huagongshe.com/reaction/2362888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetamideHCID 6580—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl 4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decane-8-carboxylateHCID 389488—
SolventDimethylformamideHCID 6228—
ProductHCID 58046811HCID 5804681198%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of tert-butyl 4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decane-8-carboxylate (0.2 g, 0.43 mmol) and potassium carbonate (0.089 g, 0.65 mmol) in N,N-dimethylformamide (3 mL), was added chloroacetamide (0.04 g, 0.43 mmol). After stirring at 65° C. for 18 hours, the reaction mixture was diluted with ethyl acetate (25 mL), washed with dilute citric acid, water and brine. The organic phase was dried over MgSO4, filtered and isolated by Biotage flash chromatography (2-10% methanol/dichloromethane) to obtain the title compound (0.22 g, 98%); 1H NMR (DMSO-d6): δ 1.45 (s, 9H), 1.65 (d, 2H, J=13.2 Hz), 2.32-2.45 (m, 2H), 3.50 (br, 2H), 3.88 (br, 2H), 4.62-4.66 (m, 6H), 6.68 (d, 2H, J=8 Hz), 6.77 (t, 1H, J=7.6 Hz), 7.17 (t, 2H, J=8.4 Hz), 7.30 (s, 1H), 7.54-7.62 (m, 3H), 7.95-7.98 (m, 2H); MS for C28H34N4O6 m/z 523.04 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691836B2
Source datasetuspto-grants-2014_04
ORD IDord-50c45a43119b45da88a20c9b7aab8603
Source noteuspto-grants-2014_04