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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492803Generated: November 1, 2026

HCID 15200286, compound → HCID 57211577, compound

https://huagongshe.com/reaction/1492803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15200286HCID 15200286—
ReactantHCID 88456900HCID 88456900—
SolventAcetonitrileHCID 6342—
SolventDiisopropylethylamineHCID 81531—
ProductHCID 57211577HCID 5721157769.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of p-nitrobenzyl (1R,5S,6S)-2-diphenoxyphosphoryloxy-6-[(R)-1-hydroxyethyl]-1-methyl-1-carbapen-2-em-3-carboxylate (2.50 g, 4.2 mmol) in acetonitrile (60ml), N,N-diisopropylethylamine was dropwise added in a nitrogen stream under cooling with ice, followed by dropwise adding a solution of (2S,4S)-4-mercapto-2-(N-methylpiperidin-4-yl)-N-(p-nitrobenzyloxycarbonyl)pyrrolidine trifluoroacetic acid salt (2.30 g, 4.6 mmol, compound of Reference Example 37 in acetonitrile (60 ml). After the mixture was stirred at 0° C. for 15 hours, the precipitate was collected by filtration, washed with acetonitrile and dried to obtain p-nitrobenzyl (1R,5S,6S)-6-[(R)-1-hydroxyethyl]-1-methyl-2 -[(2S,4S)-2-(N-methylpiperidin-4-yl)pyrrolidin-4-ylthio]-1-carbapen-2-em-3-carboxylate (2.12 g, yield: 69.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05374720
Source datasetuspto-grants-1994_12
ORD IDord-23870bb9f9f046d8af2e51aeaf4420f8
Source noteuspto-grants-1994_12