Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269682Generated: October 29, 2026

Benzyl[(1S)-4-[(tert-butoxycarbonyl)amino]-1-({[(1S)-2-[(tert-butoxycarbonyl)amino]-1-(hydroxymethyl)ethyl]amino}carbonyl)butyl]carbamate → N5-(tert-Butoxycarbonyl)-N-[(1S)-2-[(tert-butoxycarbonyl)amino]-1-(hydroxymethyl)ethyl]-L-ornithinamide

https://huagongshe.com/reaction/269682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl[(1S)-4-[(tert-butoxycarbonyl)amino]-1-({[(1S)-2-[(tert-butoxycarbonyl)amino]-1-(hydroxymethyl)ethyl]amino}carbonyl)butyl]carbamateHCID 131727171—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN5-(tert-Butoxycarbonyl)-N-[(1S)-2-[(tert-butoxycarbonyl)amino]-1-(hydroxymethyl)ethyl]-L-ornithinamideHCID 86619443—

Reaction Steps

40 mg of palladium on activated carbon (10%) are added to a mixture of 0.216 g (0.40 mmol) of the compound from Example 252A in 10 ml of ethanol, and the mixture is then hydrogenated under atmospheric pressure for 12 h. The reaction mixture is filtered through kieselguhr, and the filtrate is concentrated in vacuo and dried under high vacuum. The crude product is reacted without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446102B2
Source datasetuspto-grants-2008_11
ORD IDord-78b71b2091d740ad9f2b7c7527e96b08
Source noteuspto-grants-2008_11