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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215872Generated: October 29, 2026

{4-[3-((R)-1-Benzyl-pyrrolidin-3-yl)-ureido]-cyclohexyl}-carbamic acid tert-butyl ester → [4-((R)-3-Pyrrolidin-3-ylureido)-cyclohexyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/215872

Reaction equation

Participants

RoleNameHCIDCharge
Reactant{4-[3-((R)-1-Benzyl-pyrrolidin-3-yl)-ureido]-cyclohexyl}-carbamic acid tert-butyl esterHCID 67022947—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
Product[4-((R)-3-Pyrrolidin-3-ylureido)-cyclohexyl]-carbamic acid tert-butyl esterHCID 58025036—

Reaction Steps

To a solution of {4-[3-((R)-1-Benzyl-pyrrolidin-3-yl)-ureido]-cyclohexyl}-carbamic acid tert-butyl ester in ethanol under an inert atmosphere of argon is added palladium hydroxide on carbon. The reaction mixture is purged with argon and placed under an atmosphere of hydrogen for over night. The mixture is filtered and the catalyst washed with ethanol. The organic portions are combined and concentrated in vacuo to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193164B2
Source datasetuspto-grants-2012_06
ORD IDord-a54a53c6fcf44a1295e36d51b740b374
Source noteuspto-grants-2012_06