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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269627Generated: October 26, 2026

Benzyl[(1S)-2-({3-[(tert-butoxycarbonyl)amino]-2-hydroxypropyl}amino)-1-(hydroxymethyl)-2-oxoethyl]carbamate → N-{3-[(tert-Butoxycarbonyl)amino]-2-hydroxypropyl}-L-serinamide

https://huagongshe.com/reaction/269627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl[(1S)-2-({3-[(tert-butoxycarbonyl)amino]-2-hydroxypropyl}amino)-1-(hydroxymethyl)-2-oxoethyl]carbamateHCID 131727151—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN-{3-[(tert-Butoxycarbonyl)amino]-2-hydroxypropyl}-L-serinamideHCID 86619427—

Reaction Steps

131 mg (0.318 mmol) of benzyl[(1S)-2-({3-[(tert-butoxycarbonyl)amino]-2-hydroxypropyl}amino)-1-(hydroxymethyl)-2-oxoethyl]carbamate (Example 100A) are dissolved in 20 ml of ethanol. 20 mg of palladium on activated carbon (10%) are added thereto, and the mixture is hydrogenated under atmospheric pressure for 15 h. The reaction mixture is filtered through prewashed kieselguhr, and the filtrate is concentrated in vacuo on a rotary evaporator. 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-cf54cee1f4db40239d57e0ac1d8884b1
Source noteuspto-grants-2008_11