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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1156267Erstellt: 27. Oktober 2026

5-Nitroso-2,4,6-pyrimidinetriamine → 2,4,7-Triamino-6-(p-acetoxyphenyl)-pteridine

https://huagongshe.com/reaction/1156267

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-Nitroso-2,4,6-pyrimidinetriamineHCID 70504—
EduktSodiumHCID 5360545—
Eduktp-AcetoxybenzylcyanideHCID 15628731—
LösungsmittelGlycol monoethyl etherHCID 8076—
Produkt2,4,7-Triamino-6-(p-acetoxyphenyl)-pteridineHCID 20535715—

Reaktionsschritte

410 mg metallic sodium were dissolved while stirring in 100 ml of 2-ethoxy ethanol. Thereafter, 1100 mg 2,4,6-Triaminonitrosopyrimidine are added while stirring together with 1140 mg p-acetoxybenzylcyanide and the mixture is heated while stirring up to the boiling point. The color of the mixture changed from violet to brown. After two hours boiling under reflux, the heat is turned off and the reaction mixture is allowed to cool. Thereafter, 70 to 80% of the 2-ethoxyethanol is distilled under the vacuum of the water system, and the residue is taken up in 500 mls of water. After four-fold extraction with ether the pH is adjusted to pH 5 with 2 N hydrochloric acid. The precipitate is filtered, it is washed with a small amount of ice-cold acetone and recrystallized from 10% acetic acid. Further purification can be carried out over a silica gel column. The title compound obtained melts at 319°-321° C. (carbonization).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04335119
Quelldatensatzuspto-grants-1982_06
ORD IDord-55bfc357f67043e7bcb11c0e856a2e0e
Quellennotizuspto-grants-1982_06