Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644340Generated: October 30, 2026

HCID 10101472, compound → HCID 11764742, compound

https://huagongshe.com/reaction/644340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10101472HCID 10101472—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 11764742HCID 11764742—

Reaction Steps

A solution of 100 mg (0.14 mmol) 4-(2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl)-piperidine-1-carboxylic acid [(R)-2-[4-(1-benzyl-piperidin-4-yl)-piperazin-1-yl]-2-oxo-1-(5,6,7,8-tetrahydro-naphthalen-2-ylmethyl)-ethyl]-amide (Example 50) in 10 mL MeOH was hydrogenated in the presence of 20 mg Pd/C (10%) at 50° C. and 3 bar hydrogen pressure until the calculated volume of hydrogen had been taken up. The catalyst was filtered off, the solvent eliminated under reduced pressure and the residue purified by chromatography on silica gel. The product fractions were evaporated down under reduced pressure and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700589B2
Source datasetuspto-grants-2010_04
ORD IDord-0eacfc883a9042bdb809ddd98dd3432f
Source noteuspto-grants-2010_04