HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356736Generated: October 26, 2026
Hydrogen Peroxide → 2-Acetamido-6-diphenylcarbamoyl-9-(vinyloxymethyl)purine
https://huagongshe.com/reaction/356736
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Acetamido-6-diphenylcarbamoyl-9-[2-(phenylselenyl)ethoxymethyl]purine | HCID 18939372 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Acetamido-6-diphenylcarbamoyl-9-(vinyloxymethyl)purine | HCID 18939420 | — |
Reaction Steps
To a solution of 2-acetamido-6-diphenylcarbamoyl-9-[2-(phenylselenyl)ethoxymethyl]purine (4.92 g, 8.16 mmol) in dioxane (80 mL) was added 30% H2O2 (4 mL, 35 mmol) and sodium bicarbonate (2.1 g, 24.5 inmol). The mixture was heated at 60° C. for 20 min. The reaction was then concentrated to about 10 mL, diluted with ethyl acetate (100 mL), dried (MgSO4) and the solvents were removed in vacuo. The residue was dissolved in dioxane (40 mL), diisopropylethylamine (1.27 g, 10 mmol) was added and the solution was heated at 80° C. for 30 min under nitrogen. The solvent was evaporated in vacuo and the residual oil was chromatographed on silica gel using CH2Cl2 -ethyl acetate (1:1) as eluent to give the title compound as a yellowish powder: yield 2.3 g (65%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05837871 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-5fee0f087a76409297dd1a6872818ac4 |
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| Source note | uspto-grants-1998_11 |
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