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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289041Generated: October 31, 2026

p-nitrobenzyl (1R,5R,6S)-2-(di-phenylphosphoryloxy)-6-[(R)-1-hydroxyethyl]-1-methyl-carbapen-2-em-3-carboxylate → HCID 178462281, compound

https://huagongshe.com/reaction/2289041

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-nitrobenzyl (1R,5R,6S)-2-(di-phenylphosphoryloxy)-6-[(R)-1-hydroxyethyl]-1-methyl-carbapen-2-em-3-carboxylateHCID 15871605—
ReactantHCID 178511205HCID 178511205—
ProductHCID 178462281HCID 17846228173.3%

Reaction Steps

By using 4-nitrobenzyl (1R,5R,6S)-6-[(1R)-1-hydroxyethyl]-1-methyl-2-(diphenylphosphoryloxy)-1-carbapen-2-em-3-carboxylate (563.2 mg) and (2S,4S)-2-[1-hydroxy-2-[(3S)-3-(4-nitrobenzyloxycarbonylacetimidoylamino)pyrrolidin-1-ylcarbonyl]ethyl]-4-mercapto-1-(4-nitrobenzyloxycarbonyl)pyrrolidine (594.3 mg), reaction and purification were carried out in a similar manner to that described in Example 40-(1), whereby 4-nitrobenzyl (1R,5S,6S)-6-[(1R)-1-hydroxyethyl]-2-[(2S,4S)-2-[(3S)-3-(4-nitrobenzyloxycarbonylacetimidoylamino)pyrrolidin-1-ylcarbonyl]ethyl-1-(4-nitrobenzyloxycarbonyl)pyrrolidin-4-ylthio]-1-methyl-1-carbapen-2-em-3-carboxylate (653.2 mg) was obtained as an amorphous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090802
Source datasetuspto-grants-2000_07
ORD IDord-74d3174de25e477dadd623cad659d976
Source noteuspto-grants-2000_07