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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492323Generated: October 31, 2026

HCID 15200286, compound → HCID 57212754, compound

https://huagongshe.com/reaction/1492323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15200286HCID 15200286—
ReactantHCID 131718795HCID 131718795—
ProductHCID 57212754HCID 5721275457.3%

Reaction Steps

The same procedure as in Example 1-1) was carried out by using (2S, 4S)-2-[3-hydroxymethyl-N-(p-nitrobenzyloxycarbonyl)pyrrolidin-4-yl]-4-mercapto-N-(p-nitrobenzyloxycarbonyl)pyrrolidine diastereomer A (3.34 g, 5.42 mmol, compound of Reference Example 5) and p-nitrobenzyl (1R, 5S, 6S)-2-diphenoxyphosphoryloxy-6-[(R)-1-hydroxyethyl]-1-methyl-1-carbapen-2-em-3-carboxylate (3.22 g, 5.42 mmol) to obtain p-nitrobenzyl (1R, 5S, 6S)- 6-[(R)-1-hydroxyethyl]-2-[(2S,4S)-2-[3-hydroxymethyl-N-(p-nitrobenzyloxycarbonyl)pyrrolidin-4-yl]-N-(p-nitrobenzyloxycarbonyl)pyrrolidin-4-ylthio]-1-methyl-1-carbapen-2-em-3-carboxylate diastereomer A (2.81 g, yield: 57.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05373002
Source datasetuspto-grants-1994_12
ORD IDord-e0b770d52d0a429288a272b041f5964c
Source noteuspto-grants-1994_12