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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546598Generated: October 30, 2026

N-(2-Aminoethyl)piperidine → HCID 67198669, compound

https://huagongshe.com/reaction/546598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-Aminoethyl)piperidineHCID 33944—
Reactant3-(4-tert-butylphenyl)-5,5-dimethyl-1-[(2-thioxo-2H-[1,2,4]oxadiazolo[2,3-a]pyridin-7-yl)methyl]imidazolidine-2,4-dioneHCID 57625975—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67198669HCID 67198669—

Reaction Steps

A solution of 100 mg of 3-(4-tert-butylphenyl)-5,5-dimethyl-1-[(2-thioxo-2H-[1,2,4]oxadiazolo[2,3-a]pyridin-7-yl)methyl]imidazolidine-2,4-dione obtained in stage b) of Example 9 in 2 mL of dioxane and 36 μl of 1-(2-aminoethyl)piperidine is heated by microwave at 130° C. for 15 minutes. The reaction mixture is concentrated under reduced pressure and the residue is purified by HPLC (gradient: water/acetonitrile containing 0.1% formic acid) to give 75 mg of 1-(4-{[3-(4-tert-butylphenyl)-5,5-dimethyl-2,4-dioxo-imidazolidin-1-yl]methyl}pyridin-2-yl)-3-(2-piperidin-1-ylethyl)urea, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935819B2
Source datasetuspto-grants-2011_05
ORD IDord-367caf7f67854bd3920efcfad9f1c83e
Source noteuspto-grants-2011_05