HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737260Generated: October 27, 2026
Triphenylphosphine → 4(3H)-Pteridinone, 2-methyl-3-(o-tolyl)-
https://huagongshe.com/reaction/1737260
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 3-Acetamidopyrazine-2-carboxylic acid o-toluamide | HCID 69709772 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4(3H)-Pteridinone, 2-methyl-3-(o-tolyl)- | HCID 210797 | — |
Reaction Steps
To a mixture of 3-acetamidopyrazine-2-carboxylic acid o-toluamide (1.0 g, 3.70 mmol), triphenylphosphine (2.91 g, 11.1 mmol), and 4-dimethylaminopyridine (0.045 g, about 10 mol %) in dioxane (45 mL) was added diethyl azodicarboxylate (1.75 mL, 11.1 mmol) dropwise via syringe. The reaction was refluxed overnight, cooled to ambient temperature and concentrated. The residue was partitioned between methylene chloride and water. The phases were separated and the organic layer was washed with brine, dried and concentrated. The residue was flash chromatographed on silica gel (2.25×4 inches, packed in hexane) with elution proceeding as follows: 20%-80% ethyl acetate/hexane, forerun; 85% ethyl acetate/hexane (1000 mL), 0.71 g (76%) of 2-methyl-3-(2-methyl-phenyl)-3H-pteridin-4-one which was suitable for use without further purification. A sample was recrystallized from ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05962457 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-4f7b91f867c54121b08b32faa9dbbf07 |
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| Source note | uspto-grants-1999_10 |
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