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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490361Generated: November 2, 2026

HCID 11143993, compound → 4-Nitrobenzyl (1R, 5S,6S)-2-[(3S,5S)-5-[3-(S)-(4-nitrobenzyloxycarbonyl)aminopyrrolidin-1-ylcarbonyl]-1-methylpyrrolidin-3-ylthio)-6-[1(R)-hydroxyethyl]-1-methyl-1-carbapen-2-em-3-carboxylate

https://huagongshe.com/reaction/1490361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11143993HCID 11143993—
ReactantHCID 57036270HCID 57036270—
Product4-Nitrobenzyl (1R, 5S,6S)-2-[(3S,5S)-5-[3-(S)-(4-nitrobenzyloxycarbonyl)aminopyrrolidin-1-ylcarbonyl]-1-methylpyrrolidin-3-ylthio)-6-[1(R)-hydroxyethyl]-1-methyl-1-carbapen-2-em-3-carboxylateHCID 1100716360%

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 (2S,4S)-4-mercapto-2-[3(S)-(4-nitrobenzyloxycarbonyl)aminopyrrolidin-1-yl-carbonyl]-1-methylpyrrolidine 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 60%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05681951
Source datasetuspto-grants-1997_10
ORD IDord-128b023cb37b44219393c423c1ead0e0
Source noteuspto-grants-1997_10