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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614286Generated: October 25, 2026

Ro 31-8875 → 2-[3(S)-[(L-asparaginyl)amino]-2(R)-hydroxy-4-phenylbutyl]-N-tert.butyl-decahydro(4aS,8aS)-isoquinoline-3(S)-carboxamide

https://huagongshe.com/reaction/1614286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantRo 31-8875HCID 453680—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-[3(S)-[(L-asparaginyl)amino]-2(R)-hydroxy-4-phenylbutyl]-N-tert.butyl-decahydro(4aS,8aS)-isoquinoline-3(S)-carboxamideHCID 1009802399.5%

Reaction Steps

A solution of 195 mg of 2-[3(S)-[[N-(benzyloxycarbonyl)-L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N-tert.butyl-decahydro-(4aS,8aS)-isoquinoline-3(S)-carboxamide in 20 ml of ethanol was hydrogenated at room temperature and atmospheric pressure for 18 hours over 10 mg of 10% palladium-on-charcoal. The catalyst was filtered off and the filtrate was evaporated under reduced pressure to give 154 mg of 2-[3(S)-[(L-asparaginyl)amino]2(R)-hydroxy-4-phenylbutyl]-N-tert.butyl-decahydro-(4aS,8aS)-isoquinoline-3(S)-carboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05196438
Source datasetuspto-grants-1993_03
ORD IDord-f14bc7487ffc4ec9b2c49e712db6ed79
Source noteuspto-grants-1993_03