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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010563Generated: October 31, 2026

(3S,4S)-1-Benzyloxycarbonyl-3-(tert-butoxycarbonyl)amino-4-cyclopropylpyrrolidine → (3S,4S)-3-(tert-Butoxycarbonyl)amino-4-cyclopropylpyrrolidine

https://huagongshe.com/reaction/1010563

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3S,4S)-1-Benzyloxycarbonyl-3-(tert-butoxycarbonyl)amino-4-cyclopropylpyrrolidineHCID 53837949—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
Product(3S,4S)-3-(tert-Butoxycarbonyl)amino-4-cyclopropylpyrrolidineHCID 22871839—

Reaction Steps

A 10% palladium carbon catalyst (50 mg) was added to a solution of (3S,4S)-1-benzyloxycarbonyl-3-(tert-butoxycarbonyl)amino-4-cyclopropylpyrrolidine (408 mg, 1.13 mmol) in ethanol (5 mL), followed by stirring in a hydrogen atmosphere under an ordinary pressure at 45° C. for 12 hours. After filtration, the filtrate was concentrated under reduced pressure, to thereby yield the title compound as a colorless oily substance (255 mg, quantitative amount). The product was employed, without further purification, in the subsequent step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977327B2
Source datasetuspto-grants-2011_07
ORD IDord-8d3baf5dce114a699c08afdc76681bd1
Source noteuspto-grants-2011_07