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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269669Generated: October 27, 2026

Benzyl {(1S)-1-[2-({(2S)-2,5-bis[(tert-butoxycarbonyl)amino]pentyl}amino)-2-oxoethyl]-4-[(tert-butoxycarbonyl)amino]butyl}carbamate → Tert-butyl[(4s)-4-amino-6-({(2s)-2,5-bis[(tert-butoxycarbonyl)amino]pentyl}amino)-6-oxohexyl]carbamate

https://huagongshe.com/reaction/269669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl {(1S)-1-[2-({(2S)-2,5-bis[(tert-butoxycarbonyl)amino]pentyl}amino)-2-oxoethyl]-4-[(tert-butoxycarbonyl)amino]butyl}carbamateHCID 86625285—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductTert-butyl[(4s)-4-amino-6-({(2s)-2,5-bis[(tert-butoxycarbonyl)amino]pentyl}amino)-6-oxohexyl]carbamateHCID 89222684—

Reaction Steps

22 mg of palladium on activated carbon (10%) are added to a mixture of 0.146 g (0.22 mmol) of the compound from Example 234A 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-5f354d0193994eb287d5042339751210
Source noteuspto-grants-2008_11