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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant3-Acetamidopyrazine-2-carboxylic acid o-toluamideHCID 69709772—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,4-DioxaneHCID 31275—
Product4(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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962457
Source datasetuspto-grants-1999_10
ORD IDord-4f7b91f867c54121b08b32faa9dbbf07
Source noteuspto-grants-1999_10