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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755749Generated: October 30, 2026

HCID 15200286, compound → HCID 57291756, compound

https://huagongshe.com/reaction/1755749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15200286HCID 15200286—
ReactantHCID 57074623HCID 57074623—
ProductHCID 57291756HCID 5729175676.3%

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 (185 mg, 0.31 mmol) and (2S,4S)-2-[2-carbamoyl-N-(p-nitrobenzyloxycarbonyl)pyrrolidin-4-yl]-4-mercapto-N-(p-nitrobenzyloxycarbonyl)pyrrolidine diastereomer III (175 mg, 0.31 mmol, compound of Reference Example 33) 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 (218 mg, yield: 76.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05438054
Source datasetuspto-grants-1995_08
ORD IDord-1a6e7706c14d4de2a74b2c98c4a8efb2
Source noteuspto-grants-1995_08