Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750964Generated: October 30, 2026

Chloroacetamide → HCID 58046811, compound

https://huagongshe.com/reaction/1750964

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 numberUS09156840B2
Source datasetuspto-grants-2015_10
ORD IDord-9f28fa57d7094bb89b4bf9fe54c4bf4b
Source noteuspto-grants-2015_10