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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120962Generated: November 1, 2026

Hydantoin → 1,3,8-Triazaspiro[4.5]decane-2,4-dione

https://huagongshe.com/reaction/2120962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydantoinHCID 10006—
ReactantBenzyl 2,4-dioxo-1,3,8-triazaspiro[4.5]decane-8-carboxylateHCID 10425057—
ReactantBenzyl 2-oxopiperidine-1-carboxylateHCID 11096497—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
Product1,3,8-Triazaspiro[4.5]decane-2,4-dioneHCID 120989—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 14.6 g (48.1 mmol) benzyl 2,4-dioxo-1,3,8-triaza-spiro[4.5]decan-8-carboxylate (prepared from N-(benzyloxycarbonyl)piperidone by the method from J. Med. Chem. 1995, 38, 3772) in 250 ml dry ethanol were added 500 mg 10% Pd/C, and the mixture was filled into an autoclave. After stirring at 60° C. and 10 atm of hydrogen for 3 h no starting hydantoin could be detected by TLC. A precipitate had been formed which was redissolved by addition of 100 ml acetic acid. The catalyst was removed by filtration and the solution was concentrated in vacuo. Aqueous sodium bicarbonate solution was added until the mixture became a clear solution, and the title compound precipitated in two crops upon concentration in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06693109B2
Source datasetuspto-grants-2004_02
ORD IDord-2ef4ff59461a445fb192db4930473211
Source noteuspto-grants-2004_02