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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186173Generated: November 2, 2026

HCID 86586605, compound → HCID 23447342, compound

https://huagongshe.com/reaction/2186173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86586605HCID 86586605—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 23447342HCID 2344734271%

Reaction Steps

In ethanol (30 ml) was dissolved 4-(tert-butoxycarbonyl)-1-[1-(6-chloro-4-pyrimidinyl)-4-hydroxypiperidin-4-ylmethyl]piperazin-2-one (808 mg), and to the solution was added 10% palladium on carbon (containing 50% water, 242 mg). Under hydrogen atmosphere, the mixture was vigorously stirred overnight, and the catalyst was removed. The solvent was evaporated under reduced pressure, and the residue was purified with silica gel column chromatography (eluent:methanol/ethyl acetate=1/10) to give colorless amorphous of 4-(tert-butoxycarbonyl)-1-[4-hydroxy-1-(4-pyrimidinyl)piperidin-4-ylmethyl]piperazin-2-one (527 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403595B1
Source datasetuspto-grants-2002_06
ORD IDord-e7d3e7f43e934ee3bb7cd676e202893f
Source noteuspto-grants-2002_06