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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730691Generated: October 29, 2026

HCID 67273259, compound → HCID 57832557, compound

https://huagongshe.com/reaction/730691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67273259HCID 67273259—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductHCID 57832557HCID 57832557—

Reaction Steps

A suspension of 222 mg (0.30 mmol) (R)-2-[4-(4-benzyl-piperazin-1-yl)-piperidin-1-yl]-1-(4-hydroxy-3-methoxy-5-methyl-benzyl)-2-oxo-ethyl 4-(2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl)-piperidine-1-carboxylate (Example 10.3) and 60 mg 10% Pd/C in 10 mL EtOH and 6 mL MeOH was hydrogenated at 60 psi and RT for 72 h. The catalyst was filtered off and the crude product was purified by HPLC-MS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582625B2
Source datasetuspto-grants-2009_09
ORD IDord-4bed8d2e46884ff2b92133c73e4ab966
Source noteuspto-grants-2009_09