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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730662Generated: October 30, 2026

HCID 136347862, compound → HCID 135540794, compound

https://huagongshe.com/reaction/730662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 136347862HCID 136347862—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 135540794HCID 135540794—

Reaction Steps

A solution of 51 mg (0.07 mmol) (R)-2-(1′-benzyl-4,4′-bipiperidinyl-1-yl)-1-(4-hydroxy-3,5-dimethyl-benzyl)-2-oxo-ethyl 4-(5-oxo-3-phenyl-4,5-dihydro-1,2,4-triazol-1-yl)-piperidine-1-carboxylate (Example 2.7) in 10 mL MeOH was combined with 5 mg 10% Pd/C and hydrogenated at RT and 3 bar hydrogen pressure until the reaction came to an end. The catalyst was removed by suction filtering and the residue was purified by HPLC. The fractions containing the product were combined and lyophilised.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582625B2
Source datasetuspto-grants-2009_09
ORD IDord-c907d3b9f7cc4452b6d45a59ff6b3e33
Source noteuspto-grants-2009_09