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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711193Generated: November 4, 2026

HCID 68775359, compound → HCID 68775158, compound

https://huagongshe.com/reaction/1711193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68775359HCID 68775359—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 68775158HCID 6877515894.4%

Reaction Steps

To a solution of (3-{4-[(R)-3-(2-nitro-phenyl)-2-oxo-5-phenyl-imidazolidin-1-yl]-piperidin-1-yl}-butyl)-carbamic acid tert-butyl ester (180 mg, 0.334 mmol) in CH3OH (3 ml) was added Pd/C (20 mg, 50%). The mixture was hydrogenated under H2 (2 atm.) for 10 min. Filtration and concentration gave (3-{4-[(R)-3-(2-amino-phenyl)-2-oxo-5-phenyl-imidazolidin-1-yl]-piperidin-1-yl}-butyl)-carbamic acid tert-butyl ester (160 mg, 94%). Treatment with TFA (1 ml) and CH2Cl2 (1 ml) according to general procedure C gave (R)-3-[1-(3-amino-1-methyl-propyl)-piperidin-4-yl]-1-(2-amino-phenyl)-4-phenyl-imidazolidin-2-one (114 mg, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790747B2
Source datasetuspto-grants-2010_09
ORD IDord-acf151cbc5444e8fb26a99b896581955
Source noteuspto-grants-2010_09