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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362901Generated: October 30, 2026

Dimethylformamide → HCID 58046633, compound

https://huagongshe.com/reaction/2362901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl 4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decane-8-carboxylateHCID 389488—
Reactant2-Chloro-1-(4-methylpiperazin-1-yl)ethanoneHCID 818173—
SolventEthyl AcetateHCID 8857—
ProductHCID 58046633HCID 5804663362%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of 2-chloro-1-(4-methylpiperazin-1-yl)ethanone in N,N-dimethylformamide (3 mL), was added tert-butyl 4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decane-8-carboxylate (0.2 g, 0.43 mmol) and potassium carbonate (0.119 g, 0.86 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 (2-20% methanol/dichloromethane) to obtain the title compound (0.16 g, 62%); 1H NMR (DMSO-d6): δ 1.45 (s, 9H), 1.64 (t, 2H, J=12.8 Hz), 2.18 (s, 3H), 2.25-2.45 (m, 6H), 3.41-3.50 (m, 6H), 3.85 (br, 2H), 4.60-4.65 (m, 4H), 5.05 (s, 2H), 6.64-6.69 (m, 2H), 6.76-6.79 (m, 1H), 7.13-7.19 (m, 2H), 7.54-7.60 (m, 2H), 7.91-7.93 (m, 2H); MS for C33H43N5O6 m/z 606.08 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691836B2
Source datasetuspto-grants-2014_04
ORD IDord-025e705f23de4d8b9994c3dae4bfc71d
Source noteuspto-grants-2014_04