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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642825Generated: October 30, 2026

HCID 178418361, compound → HCID 178425367, compound

https://huagongshe.com/reaction/642825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178425368HCID 178425368—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 178425367HCID 178425367—

Reaction Steps

67 mg (0.08 mmol) (R)-2-[4-(4-benzyl-piperazin-1-yl)-piperidin-1-yl]-1-(7-methyl-1H-benzimidazol-5-ylmethyl)-2-oxo-ethyl 4-(2-oxo-1,2,4,5,-tetrahydro-1,3-benzodiazepin-3-yl)-piperidine-1-carboxylate were dissolved in 10 mL MeOH and combined with 30 mg 10% Pd/C. The mixture was hydrogenated for 3 h in a Parr apparatus at 50° C. and 50 psi hydrogen pressure. Then the catalyst was filtered off and the filtrate was evaporated down i.vac. The residue was purified by HPLC, the fractions containing the product were combined and lyophilised.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696195B2
Source datasetuspto-grants-2010_04
ORD IDord-4b98a5f73b3945a4880b6513e526ce6a
Source noteuspto-grants-2010_04