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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156733Generated: October 30, 2026

HCID 12961573, compound → HCID 14782606, compound

https://huagongshe.com/reaction/1156733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 12961573HCID 12961573—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventPhosphateHCID 1061—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 14782606HCID 1478260639%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04337199
Source datasetuspto-grants-1982_06
ORD IDord-94a142e6e3774f66b896b696d808f187
Source noteuspto-grants-1982_06