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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755735Generated: November 1, 2026

HCID 15200286, compound → HCID 15200292, compound

https://huagongshe.com/reaction/1755735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15200286HCID 15200286—
ReactantHCID 15200299HCID 15200299—
ProductHCID 15200292HCID 1520029292%

Reaction Steps

The same procedure as in Example 1-1 was carried out by using p-nitrobenzyl (1R,5S,6S)-2-diphenoxyphosphoryloxy-6-[(R)-1-hydroxyethyl]-1-methyl-1-carbapen-2-em-3-carboxylate (1.75 g, 2.94 mmol) and (2S,4S)-4-mercapto-N-(p-nitrobenzyloxycarbonyl)-2-[N-(p-nitrobenzyloxycarbonyl)pyrrolidin-3-yl]pyrrolidine diastereomer A (1.56 g, 2.94 mmol, compound of Reference Example 15-7) to obtain p-nitrobenzyl (1R,5S,6S)-6-[(R)-1-hydroxyethyl]-1-methyl-2-[(2S,4S)-N-(p-nitrobenzyloxycarbonyl)-2-[N-(p-nitrobenzyloxycarbonyl)pyrrolidin-3-yl]pyrrolidin-4-ylthio]-1-carbapen-2-em-3-carboxylate diastereomer A (2.37 g, yield: 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05438054
Source datasetuspto-grants-1995_08
ORD IDord-459c1e60871e41b5b908f2947291c8da
Source noteuspto-grants-1995_08