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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18535Erstellt: 24. Oktober 2026

Ammonia → 1-(4-Aminophenyl)pyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/de/reaction/18535

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
Edukt1-(4-Nitrophenyl)pyrimidine-2,4-dioneHCID 11276338—
EduktHCID 178418361HCID 178418361—
KatalysatorNickelHCID 935—
LösungsmittelMethanolHCID 887—
Produkt1-(4-Aminophenyl)pyrimidine-2,4(1H,3H)-dioneHCID 67012135—

Reaktionsschritte

To a solution of 1.4 g 1-(4-Nitro-phenyl)-1H-pyrimidine-2,4-dione in 120 mL MeOH, 15 g Raney Nickel (washed three times with MeOH) were introduced under a nitrogen atmosphere. Then 15 mL of a 7 M solution of NH3 in MeOH were added. The nitrogen atmosphere was replaced by a hydrogen atmosphere and the mixture was hydrogenated under normal pressure at RT. After 2 h the reaction mixture was filtered through a pad of celite. The solvents were removed under reduced pressure and the residue was subjected to the next reaction step without further purification. Yield: 502 mg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741341B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-74c37d52c2334b12bb37a8433b13fbdd
Quellennotizuspto-grants-2010_06