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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269673Generated: October 29, 2026

Benzyl{(1S)-4-[(tert-butoxycarbonyl)amino]-1-[({(3S)-3-[(tert-butoxycarbonyl)amino]-4-hydroxybutyl}amino)carbonyl]butyl}carbamate → N5-(tert-Butoxycarbonyl)-N-{(3S)-3-[(tert-butoxycarbonyl)amino]-4-hydroxybutyl}-L-ornithinamide

https://huagongshe.com/reaction/269673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl{(1S)-4-[(tert-butoxycarbonyl)amino]-1-[({(3S)-3-[(tert-butoxycarbonyl)amino]-4-hydroxybutyl}amino)carbonyl]butyl}carbamateHCID 131727168—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN5-(tert-Butoxycarbonyl)-N-{(3S)-3-[(tert-butoxycarbonyl)amino]-4-hydroxybutyl}-L-ornithinamideHCID 86619439—

Reaction Steps

17 mg of palladium on activated carbon (10%) are added to a mixture of 0.088 g (0.16 mmol) of the compound from Example 238A 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-104f176c034a47a08122586e1a4db39e
Source noteuspto-grants-2008_11