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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879233Generated: October 26, 2026

(3R,4S,5S)-tert-butyl 4-((S)-2-(((benzyloxy)carbonyl)amino)-N,3-dimethylbutanamido)-3-methoxy-5-methylheptanoate → (3R,4S,5S)-tert-butyl 4-((S)-2-amino-N,3-dimethylbutanamido)-3-methoxy-5-methylheptanoate

https://huagongshe.com/reaction/879233

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3R,4S,5S)-tert-butyl 4-((S)-2-(((benzyloxy)carbonyl)amino)-N,3-dimethylbutanamido)-3-methoxy-5-methylheptanoateHCID 10529182—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(3R,4S,5S)-tert-butyl 4-((S)-2-amino-N,3-dimethylbutanamido)-3-methoxy-5-methylheptanoateHCID 10546343—

Reaction Steps

500 mg (1 mmol) tert.-butyl-(3R,4S,5S)-4-[{N-[(benzyloxy)carbonyl]-L-valyl}(methyl)amino]-3-methoxy-5-methylheptanoate (intermediate 1) were dissolved in 50 ml Methanol and, after adding 100 mg 10% Palladium on activated carbon, was hydrated at RT for 1 h under atmospheric pressure. The catalyst was then filtered off and the solving agents was removed in a vacuum. 370 mg (quant.) of the title compound were obtained an almost colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987209B2
Source datasetuspto-grants-2015_03
ORD IDord-7426568f3f024c88a76476761a50338d
Source noteuspto-grants-2015_03