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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260317Generated: October 31, 2026

(2S,4S)-4-Acetylthio-1-allyloxycarbonyl-2-carboxypyrrolidine → (2S,4S)-4-acetylthio-1-allyloxycarbonyl-2-(3(allyloxycarbonylmethoxymethyl)phenylcarbamoyl)pyrrolidine

https://huagongshe.com/reaction/260317

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S,4S)-4-Acetylthio-1-allyloxycarbonyl-2-carboxypyrrolidineHCID 15299255—
ReactantAllyl 3-aminobenzyloxyacetateHCID 22401146—
ReactantAllyl 3-aminophenoxyacetateHCID 22401151—
Product(2S,4S)-4-acetylthio-1-allyloxycarbonyl-2-(3(allyloxycarbonylmethoxymethyl)phenylcarbamoyl)pyrrolidineHCID 57141411—

Reaction Steps

Allyl 3-aminobenzyloxyacetate was condensed with (2S,4S)-4-acetylthio-1-allyloxycarbonyl-2-carboxypyrrolidine by the method described in example 3 for allyl 3-aminophenoxyacetate, except that crude product was purified by chromatography on silica, using a gradient from di-chloromethane to dichloromethane/diethyl ether (85:15), to give (2S,4S)-4-acetylthio-1-allyloxycarbonyl-2-(3(allyloxycarbonylmethoxymethyl)phenylcarbamoyl)pyrrolidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05527791
Source datasetuspto-grants-1996_06
ORD IDord-362d96d2bdfb4c769a021b97d5f960d9
Source noteuspto-grants-1996_06