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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755739Generated: October 29, 2026

HCID 15200286, compound → HCID 57261209, compound

https://huagongshe.com/reaction/1755739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15200286HCID 15200286—
ReactantHCID 18657912HCID 18657912—
ProductHCID 57261209HCID 5726120948.9%

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 (155.4 mg, 0.26 mmol) and (2S,4S)-4-mercapto-N-(p-nitrobenzyloxycarbonyl)-2-[3-[(p-nitrobenzyloxycarbonyl)amino]-2-pyrrolidon-4-yl]pyrrolidine (110 mg, 0.197 mmol, compound of Reference Example 20-6) to obtain p-nitrobenzyl (1R,5S,6S)-6-[(R)-1-hydroxyethyl]-1-methyl-2-[(2S,4S)-N-(p-nitrobenzyloxycarbonyl)-2-[3-[(p-nitrobenzyloxycarbonyl)amino]-2-pyrrolidon-4-yl]pyrrolidin-4-ylthio]-1-carbapen-2-em-3-carboxylate (87 mg, yield: 48.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05438054
Source datasetuspto-grants-1995_08
ORD IDord-df140b7f560b40168418d5c70b0148c9
Source noteuspto-grants-1995_08