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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080324Generated: October 31, 2026

HCID 57730432, compound → HCID 11528121, compound

https://huagongshe.com/reaction/2080324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57730432HCID 57730432—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 11528121HCID 1152812168.3%

Reaction Steps

To a solution of phenylmethyl (2S)-4-[(2′-fluoro-5′-{[({3-[(1-methyl-4-piperidinyl)methyl]phenyl}carbonyl)amino]methyl)-3-biphenylyl)methyl]-2-methyl-1-piperazinecarboxylate (120 mg, 0.18 mmol) in 5 mL of MeOH, was added 10% Pd/C (60 mg). The mixture was hydrogenated using a hydrogen balloon for 12 hours. After flittering off the catalyst, the mixture was concentrated and the residue was purified by Gilson reverse phase HPLC, eluting with acetonitrile/water/0.1% TFA (10/90 to 70/30, v/v, over 12 min), to give the title compound (65 mg, 41%). LC/MS: m/z, 529 (M+H), 1.29 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932247B2
Source datasetuspto-grants-2011_04
ORD IDord-8f09e0d0552b45a7b548ee30ee7517d7
Source noteuspto-grants-2011_04