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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780239Generated: October 30, 2026

(2S,3S)-3-(N2-benzyloxycarbonyl-L-asparaginyl)amino-2-hydroxy-4-phenylbutyric acid → (2S)-N-((1S,2S)-3-{(2S,4S)-2-[N-(tert-butyl)carbamoyl]-4-bromopyrrolidinyl}-2-hydroxy-3-oxo-1-benzylpropyl)-3-carbamoyl-2-[(phenylmethoxy)carbonylamino]propanamide

https://huagongshe.com/reaction/1780239

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S,3S)-3-(N2-benzyloxycarbonyl-L-asparaginyl)amino-2-hydroxy-4-phenylbutyric acidHCID 57125825—
Reactant(4S)-N-t-butoxycarbonyl-4-bromo-N-t-butyl-L-prolinamideHCID 67722360—
Product(2S)-N-((1S,2S)-3-{(2S,4S)-2-[N-(tert-butyl)carbamoyl]-4-bromopyrrolidinyl}-2-hydroxy-3-oxo-1-benzylpropyl)-3-carbamoyl-2-[(phenylmethoxy)carbonylamino]propanamideHCID 473125—

Reaction Steps

A procedure similar to that described in Example 1 was repeated, except that (2S,3S)-3-(N2 -benzyloxycarbonyl-L-asparaginyl)amino-2-hydroxy-4-phenylbutyric acid (prepared as described in Preparation 1) and (4S)-N-t-butoxycarbonyl-4-bromo-N-t-butyl-L-prolinamide (prepared as described in Preparation 8) were used as starting materials, in relative proportions similar to those used in that Example, to obtain the title compound as colorless powdery crystals, melting at 100°-105° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05629406
Source datasetuspto-grants-1997_05
ORD IDord-71246c0a28f240f2b93d0172df1018b1
Source noteuspto-grants-1997_05