HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156733Generated: October 30, 2026
HCID 12961573, compound → HCID 14782606, compound
https://huagongshe.com/reaction/1156733
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 12961573 | HCID 12961573 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Platinum oxide (PtO) | HCID 82844 | — |
| Solvent | Phosphate | HCID 1061 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 14782606 | HCID 14782606 | 39% |
Reaction Steps
63.4 mg of p-nitrobenzyl 3-(2-pyrimidinylthio)6-ethyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2carboxylate obtained in Example 26 was dissolved in a mixture of 3.2 ml of dioxane and 1.2 ml of a 0.1 M phosphate buffer (pH 6.86). Then, 70 mg of platinum oxide was added, and the reaction was performed at room temperature for 4 hours in a Paar reducing apparatus (hydrogen pressure 4 kg/cm2). The catalyst was removed by filtration. The filtrate and the wash liquid were combined, and after adjusting the pH of the mixture to 7.2, concentrated under reduced pressure to about 2/3 of the initial amount. Sodium chloride (2 g) was added to the concentrated solution, and water was added to adjust the total amount to 70 ml. The resulting solution was applied to a column of Diaion HP-20AG (1.1×20 cm), and eluted with 300 ml in total of an aqueous solution of acetone with the concentration of acetone varying gradually from 0 to 50% (v/v) by a concentration gradient method. The fractions were screened by high-speed liquid chromatography, and fractions having an ultraviolet absorption at λmax 300 nm were collected and lyophilized to afford 16.8 mg of the desired product (yield 39%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04337199 |
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| Source dataset | uspto-grants-1982_06 |
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| ORD ID | ord-94a142e6e3774f66b896b696d808f187 |
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| Source note | uspto-grants-1982_06 |
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