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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863353Generated: October 29, 2026

4-Sulfanylpyrrolidin-2-one → 4-Nitrobenzyl (1R,5S,6S)-2-[(RS)-5-oxo-3-pyrrolidinylthio]-6-[1(R)-hydroxyethyl]-1-methyl-1-carbapen-2-em-3-carboxylate

https://huagongshe.com/reaction/863353

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Sulfanylpyrrolidin-2-oneHCID 10129935—
ReactantHCID 57036270HCID 57036270—
Product4-Nitrobenzyl (1R,5S,6S)-2-[(RS)-5-oxo-3-pyrrolidinylthio]-6-[1(R)-hydroxyethyl]-1-methyl-1-carbapen-2-em-3-carboxylateHCID 5720821659%

Reaction Steps

Following a procedure similar to that described in Example 27(b), but using 4-nitrobenzyl (1R,5S,6S)-2-(2-diethylcarbamoylphenylsulfinyl)-1-methyl-6-[1(R)-hydroxyethyl]-1-carbapen-2-em-3-carboxylate [prepared as described in Example 27(a)] and 4-mercapto-2-oxopyrrolidine as starting materials, in relative proportions similar to those used in that Example, the title compound was obtained as a powder in a yield of 59%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05719275
Source datasetuspto-grants-1998_02
ORD IDord-ba5a63acf9f543e2b81de40aa8147ea4
Source noteuspto-grants-1998_02