Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725733Generated: November 1, 2026

HCID 86608967, compound → HCID 57529525, compound

https://huagongshe.com/reaction/1725733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86608967HCID 86608967—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 57529525HCID 57529525—

Reaction Steps

A solution of 64 mg (0.08 mmol) of (R)-2-[4-(4-benzyl-piperazin-1-yl)-piperidin-1-yl]-1-(3,5-bis-trifluoromethyl-benzyl)-2-oxo-ethyl 4-(2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl)-piperidine-1-carboxylate (Example 52) in 10 mL MeOH was combined with 50 mg 10% Pd/C and shaken for 3 h at RT and 50 psi hydrogen. The catalyst was suction filtered, the solvent was evaporated down i.vac., the residue was combined with acetonitrile and water and lyophilised.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491717B2
Source datasetuspto-grants-2009_02
ORD IDord-2ca53ecd7bbc4e2aa4e822bdad3c7b7d
Source noteuspto-grants-2009_02