HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492803Generated: November 1, 2026
HCID 15200286, compound → HCID 57211577, compound
https://huagongshe.com/reaction/1492803
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 15200286 | HCID 15200286 | — |
| Reactant | HCID 88456900 | HCID 88456900 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | HCID 57211577 | HCID 57211577 | 69.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05374720 |
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| Source dataset | uspto-grants-1994_12 |
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| ORD ID | ord-23870bb9f9f046d8af2e51aeaf4420f8 |
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| Source note | uspto-grants-1994_12 |
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