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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645312Generated: November 1, 2026

4-{4-[(5S)-5-(acetylamino-methyl)-2-oxo-oxazolidin-3-yl]-2-fluorophenoxymethyl}-4-hydroxy-piperidine-1-carboxylic acid benzylester → HCID 11164924, compound

https://huagongshe.com/reaction/1645312

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-{4-[(5S)-5-(acetylamino-methyl)-2-oxo-oxazolidin-3-yl]-2-fluorophenoxymethyl}-4-hydroxy-piperidine-1-carboxylic acid benzylesterHCID 66772711—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 11164924HCID 11164924—

Reaction Conditions

Temperature40 °C

Reaction Steps

A suspension of 31 g of 4-{4-[(5S)-5-(acetylaminomethyl)-2-oxo-oxazolidin-3-yl]-2-fluorophenoxymethyl}-4-hydroxypiperidin-1-carboxylic acid benzyl ester (MW: 515.54, 60.13 mmol) and 2.5 g of palladium (10% on activated carbon) in 310 ml of methanol and 150 ml of ethyl acetate was stirred for 4 h under a hydrogen atmosphere. The course of the reaction was monitored by TLC (ethyl acetate). The suspension was diluted with 300 ml of methanol, heated to 40° C., and the catalyst was filtered off through a fibreglass filter paper. The filtrate was concentrated to 150 ml, diluted with 300 ml of ethyl acetate and concentrated again to 200 ml. 200 ml of diethyl ether were added and the suspension was cooled, with stirring, to 0° C. The solid material was collected and dried. Yield: 21.6 g, 94.3%. MS: 382.6 (M+H)+, Method: ESI+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124772B2
Source datasetuspto-grants-2012_02
ORD IDord-83d7da9f38c241f79b3d82276a7e65ba
Source noteuspto-grants-2012_02