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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446059Generated: October 26, 2026

Piperidine → HCID 86675361, compound

https://huagongshe.com/reaction/446059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantHCID 43155822HCID 43155822—
ReactantEthyl-2-(5-oxo-2-thioxoimidazolidin-1-yl)acetateHCID 43995697—
SolventDichloromethaneHCID 6344—
ProductHCID 86675361HCID 8667536143.6%

Reaction Conditions

Temperature25 °C

Reaction Steps

5-(3-Iodophenyl)furan-2-carbaldehyde (30 mg, 0.1 mmol) synthesized by the same method as in Example 1 and ethyl-2-(5-oxo-2-thioxoimidazolidin-1-yl)acetate (20 mg, 0.1 mmol) were dissolved in dichloromethane (7 mL), piperidine (20 μL) was added thereto, and the mixture was stirred at room temperature (25° C.) overnight. After the reaction was completed the solvent was removed by evaporation under reduced pressure, and the residue was subjected to silica gel column chromatography using ethyl acetate/hexane (3/7 (volume ratio)) as an eluent, to give compound 2 in a yield of 21 mg (yield 43.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476449B2
Source datasetuspto-grants-2013_07
ORD IDord-8b5708c1b379492382885c12243bcee2
Source noteuspto-grants-2013_07