Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642823Generated: October 30, 2026

HCID 178418361, compound → HCID 178425364, compound

https://huagongshe.com/reaction/642823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178425365HCID 178425365—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 178425364HCID 178425364—

Reaction Steps

75 mg (0.09 mmol) (R)-2-(1′-benzyl-4,4′-bipiperidinyl-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 2 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696195B2
Source datasetuspto-grants-2010_04
ORD IDord-dbaf7e8e00ad42eb82763194428660e2
Source noteuspto-grants-2010_04