HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650863Generated: November 1, 2026
HCID 15056065, compound → HCID 57007843, compound
https://huagongshe.com/reaction/1650863
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 15056065 | HCID 15056065 | — |
| Reactant | Sodium Diacetate | HCID 23662384 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57007843 | HCID 57007843 | 42.2% |
Reaction Steps
A mixture of 4-nitrobenzyl (4R,5S,6S)-6-[(1R)-1-hydroxyethyl]-4-methyl-3-[(2S,4S)-1-(4-nitrobenzyloxycarbonyl)-2-{4-(4-nitrobenzyloxycarbonyl)piperazin-1-yl}methylpyrrolidin-4-yl]thio-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate (1.20 g), 20 % palladium hydroxide on carbon (0.6 g), 0.2M sodium acetate-acetic acid buffer (pH=5.8, 50 ml) and tetrahydrofuran (50 ml) was stirred for 5 hours under atmospheric pressure of hydrogen at ambient temperature. After the catalyst was filtered off, the filtrate was evaporated under reduced pressure to remove the organic solvent. The residue was chromatographed on nonionic adsorption resin, "Diaion HP-20" (trademark, made by Mitsubishi Chemical Industries) (30 ml) eluting in turn with water (80 ml) and 5% aqueous acetone (90 ml). The fractions containing the desired compound were collected and lyophilized to give (4R,5S,6S)-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-3-[(2S,4S)-2-(piperazin-1-yl)methylpyrrolidin-4-yl]thio-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid (0.23 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04925838 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-0fe45c93db5042808de7c72ab417108a |
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| Source note | uspto-grants-1990_05 |
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