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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269680Generated: October 25, 2026

Benzyl{(1S)-4-[(tert-butoxycarbonyl)amino]-1-[({(4S)-4-[(tert-butoxycarbonyl)amino]-5-hydroxypentyl}amino)carbonyl]butyl}carbamate → N5-(tert-Butoxycarbonyl)-N-{(4S)-4-[(tert-butoxycarbonyl)amino]-5-hydroxypentyl}-L-ornithinamide

https://huagongshe.com/reaction/269680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl{(1S)-4-[(tert-butoxycarbonyl)amino]-1-[({(4S)-4-[(tert-butoxycarbonyl)amino]-5-hydroxypentyl}amino)carbonyl]butyl}carbamateHCID 86625287—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN5-(tert-Butoxycarbonyl)-N-{(4S)-4-[(tert-butoxycarbonyl)amino]-5-hydroxypentyl}-L-ornithinamideHCID 86619441—

Reaction Steps

30 mg of palladium on activated carbon (10%) are added to a mixture of 0.164 g (0.29 mmol) of the compound from Example 248A 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-3057f601b94b4d54af34d1cdd699eb3b
Source noteuspto-grants-2008_11