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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725739Generated: October 30, 2026

HCID 67301686, compound → HCID 16041972, compound

https://huagongshe.com/reaction/1725739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67301686HCID 67301686—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 16041972HCID 16041972—

Reaction Steps

A solution of 54 mg (0.08 mmol) of (R)-2-[4-(1-benzyl-piperidin-4-yl)-piperazin-1-yl]-1-(4-hydroxy-3,5-dimethyl-benzyl)-2-oxo-ethyl 4-(2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl)-piperidine-1-carboxylate (Example 78) in 5 mL MeOH were combined with 20 mg of 10% Pd/C and shaken at RT and 3 bar hydrogen until the reaction stopped. The catalyst was suction filtered and the solvent evaporated down i.vac. The residue was triturated with DIPE, suction filtered and dried under a high vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491717B2
Source datasetuspto-grants-2009_02
ORD IDord-446e7b93d8344b2b9a85b028d3de530e
Source noteuspto-grants-2009_02