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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269625Generated: November 2, 2026

benzyl{(1S)-3-[(tert-butoxycarbonyl)amino]-1-[({3-[(tert-butoxycarbonyl)amino]-2-hydroxypropyl}amino)carbonyl]propyl}carbamate → Tert-butyl[3-({(2s)-2-amino-4-[(tert-butoxycarbonyl)amino]butanoyl}amino)-2-hydroxypropyl]carbamate

https://huagongshe.com/reaction/269625

Reaction equation

Participants

RoleNameHCIDCharge
Reactantbenzyl{(1S)-3-[(tert-butoxycarbonyl)amino]-1-[({3-[(tert-butoxycarbonyl)amino]-2-hydroxypropyl}amino)carbonyl]propyl}carbamateHCID 131727150—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductTert-butyl[3-({(2s)-2-amino-4-[(tert-butoxycarbonyl)amino]butanoyl}amino)-2-hydroxypropyl]carbamateHCID 89225963—

Reaction Steps

38 mg (0.12 mmol) of the compound from Example 98A are dissolved in 10 ml of methanol, and 10 mg of palladium on activated carbon (10%) are added. The mixture is hydrogenated under atmospheric pressure for 2 h and filtered through kieselguhr, and the mother liquor is concentrated in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446102B2
Source datasetuspto-grants-2008_11
ORD IDord-2ca48361dea845028d87750143e1add3
Source noteuspto-grants-2008_11