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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729293Generated: October 30, 2026

HCID 10069734, compound → HCID 10090741, compound

https://huagongshe.com/reaction/1729293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10069734HCID 10069734—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 10090741HCID 1009074183.2%

Reaction Steps

2 g of 1,3-dimethyl-6-[4-(3-[4-nitrophenoxy)propyl)piperazin-1-yl]-2,4(1H,3H)-pyrimidinedione (Compound f) obtained in Reference Example 4 was suspended in 300 ml of methanol and 500 mg of 10% Pd/c solution was added to the suspension, and hydrogenation was then carried out at ordinary pressure for 30 minutes. The catalyst was removed by filtration, and the solvent was distilled off, thereby obtaining 1.54 g of 6-[4-(3-[4-aminophenoxy)propyl)piperazin-1-yl]-1,3-dimethyl-2,4(1H,3H)-pyrimidinedione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05332739
Source datasetuspto-grants-1994_07
ORD IDord-63e02c33739a4d5fb2939d5d55514a68
Source noteuspto-grants-1994_07