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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643165Generated: October 28, 2026

HCID 68673613, compound → HCID 68673858, compound

https://huagongshe.com/reaction/643165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68673613HCID 68673613—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventTriethylamineHCID 8471—
ProductHCID 68673858HCID 68673858—

Reaction Steps

A suspension of 7.60 g (12.98 mmol) (S)-2-(4-benzyloxy-3-methoxy-5-methyl-benzyl)-4-oxo-4-[4-(2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl)-piperidin-1-yl]-butanoic acid and 0.76 g 10% Pd/C in 2 mL triethylamine and 150 mL MeOH was hydrogenated at RT and 2620 hPa hydrogen pressure for 16 h. To complete the reaction a further 0.38 g 10% Pd/C were added and the mixture was again hydrogenated for 3 h at RT. The catalyst was filtered off through Celite and the filtrate was concentrated by evaporation i.vac. The product was further reacted without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696209B2
Source datasetuspto-grants-2010_04
ORD IDord-d809daf0ae7c4fbf9d2c8975f62345a2
Source noteuspto-grants-2010_04