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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18535Generated: October 25, 2026

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

https://huagongshe.com/reaction/18535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant1-(4-Nitrophenyl)pyrimidine-2,4-dioneHCID 11276338—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Product1-(4-Aminophenyl)pyrimidine-2,4(1H,3H)-dioneHCID 67012135—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741341B2
Source datasetuspto-grants-2010_06
ORD IDord-74c37d52c2334b12bb37a8433b13fbdd
Source noteuspto-grants-2010_06