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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydantoin | HCID 10006 | — |
| Reactant | Benzyl 2,4-dioxo-1,3,8-triazaspiro[4.5]decane-8-carboxylate | HCID 10425057 | — |
| Reactant | Benzyl 2-oxopiperidine-1-carboxylate | HCID 11096497 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,3,8-Triazaspiro[4.5]decane-2,4-dione | HCID 120989 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06693109B2 |
|---|
| Source dataset | uspto-grants-2004_02 |
|---|
| ORD ID | ord-2ef4ff59461a445fb192db4930473211 |
|---|
| Source note | uspto-grants-2004_02 |
|---|