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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269641Generated: October 26, 2026

Benzyl {(1S)-1-[({(2S)-2,5-bis[(tert-butoxycarbonyl)amino]pentyl}amino)carbonyl]-4-[(tert-butoxycarbonyl)amino]butyl}carbamate → Tert-butyl[(4s)-4-amino-5-({(2s)-2,5-bis[(tert-butoxycarbonyl)amino]pentyl}amino)-5-oxopentyl]carbamate

https://huagongshe.com/reaction/269641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl {(1S)-1-[({(2S)-2,5-bis[(tert-butoxycarbonyl)amino]pentyl}amino)carbonyl]-4-[(tert-butoxycarbonyl)amino]butyl}carbamateHCID 86624497—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductTert-butyl[(4s)-4-amino-5-({(2s)-2,5-bis[(tert-butoxycarbonyl)amino]pentyl}amino)-5-oxopentyl]carbamateHCID 86624530—

Reaction Steps

Preparation takes place in analogy to Example 81A from 132 mg (0.20 mmol) of benzyl{(1S)-1-[({(2S)-2,5-bis[(tert-butoxycarbonyl)amino]pentyl}amino)carbonyl]-4-[(tert-butoxycarbonyl)amino]butyl}carbamate (Example 119A) in 50 ml of ethanol with the addition of 13 mg of palladium on activated carbon (10%). The product is reacted without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446102B2
Source datasetuspto-grants-2008_11
ORD IDord-d298cf61992643f98bff20aa0711c269
Source noteuspto-grants-2008_11