HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1590510Generated: October 31, 2026
(R)-4-Nitrobenzyl 2-diazo-4-((2R,3S)-3-((R)-1-hydroxyethyl)-4-oxoazetidin-2-yl)-3-oxopentanoate → 1-Azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[(1R)-1-hydroxyethyl]-4-methyl-3,7-dioxo-, (4-nitrophenyl)methyl ester, (4R,5R,6S)-
https://huagongshe.com/reaction/1590510
Participants
| Role | Name | HCID | Charge |
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| Reactant | (R)-4-Nitrobenzyl 2-diazo-4-((2R,3S)-3-((R)-1-hydroxyethyl)-4-oxoazetidin-2-yl)-3-oxopentanoate | HCID 57009450 | — |
| Catalyst | Acetic acid, rhodium(2+) salt | HCID 21674 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[(1R)-1-hydroxyethyl]-4-methyl-3,7-dioxo-, (4-nitrophenyl)methyl ester, (4R,5R,6S)- | HCID 9885302 | — |
Reaction Steps
To a solution of 4-nitrobenzyl (4R)-2-diazo-4-[(2R,3S)-3-{(1R)-1-hydroxyethyl}-4-oxoazetidin-2-yl]-3-oxopentanoate (1.50 g) in 1,2-dichloroethane (30 ml) was added rhodium(II) acetate (5 mg) under refluxing. After refluxing for 30 minutes, the reaction mixture was cooled and evaporated in vacuo to give a residue. The residue was dissolved in anhydrous acetonitrile (10 ml) and then evaporated. This operation was repeated once again and the residue was dried in vacuo to give 4-nitrobenzyl (4R,5R,6S)-6-[(1R)-1-hydroxyethyl]-4-methyl-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate. The compound obtained was dissolved in anhydrous acetonitrile (30 ml) and cooled to 0° C. under an atmosphere of nitrogen. To this solution were added diphenyl phosphorochloridate (0.84 ml) and N,N-diisopropyl-N-ethylamine (0.74 ml) successively and the solution was stirred at 0° C. for 40 minutes. To the resulting solution were added dropwise a solution of (2S,4S)-4-mercapto-2-(4-methylpiperazin-1-yl)methyl-1-(4-nitrobenzyloxycarbonyl)pyrrolidine (1.97 g) in acetonitrile (10 ml) and N,N-diisopropyl-N-ethylamine (0.87 ml) with stirring at 5° C., and the stirring was continued at the same temperature for 2 hours. To the reaction mixture was added ethyl acetate (50 ml) and water (20 ml) with stirring, and the organic layer was separated. This layer was washed with saturated aqueous sodium chloride solution (40 ml×3), dried over magnesium sulfate and evaporated. The residue was chromatographed on silica gel (100 g) eluting with a mixture of chloroform and methanol (9:1 V/V). The fractions containing the desired compound were collected and evaporated in vacuo to give 4-nitrobenzyl (4R,5S,6S)-6-[(1R)-1-hydroxyethyl]-3-[(2S,4S)-2-(4-methylpiperazin-1-yl)methyl-1-(4-nitrobenzyloxycarbonyl)pyrrolidin-4-yl]thio-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate (2.38 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05202437 |
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| Source dataset | uspto-grants-1993_04 |
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| ORD ID | ord-a04ef523853b46e580e27737bb5a3eb1 |
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| Source note | uspto-grants-1993_04 |
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