Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755733Generated: October 31, 2026

HCID 15200286, compound → HCID 57291756, compound

https://huagongshe.com/reaction/1755733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15200286HCID 15200286—
ReactantHCID 57074623HCID 57074623—
ReactantHCID 131718807HCID 131718807—
ProductHCID 57291756HCID 57291756—

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 (290 mg, 0.49 mmol) and (2S,4S)-2-[2-carbamoyl-N-(p-nitrobenzyloxycarbonyl)pyrrolidin-4-yl]-4-mercapto-N-(p-nitrobenzyloxycarbonyl)pyrrolidine diastereomer II (280 mg, 0.49 mmol, compound of Reference Example 14) to obtain p-nitrobenzyl (1R,5S,6S)-2-[(2S,4S)-2-[2-carbamoyl-N-(p-nitrobenzyloxycarbonyl)pyrrolidin-4-yl]-N-(p-nitrobenzyloxycarbonyl)pyrrolidin-4-ylthio]-6-[(R)-1-hydroxyethyl]-1-methyl-1-carbapen-2-em-3-carboxylate diastereomer II (419 mg, yield: 93.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05438054
Source datasetuspto-grants-1995_08
ORD IDord-ff78b557f46c46c0858e8ff8426d806d
Source noteuspto-grants-1995_08