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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353135Generated: October 30, 2026

HCID 9911005, compound → HCID 22707383, compound

https://huagongshe.com/reaction/353135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 9911005HCID 9911005—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 22707383HCID 2270738329%

Reaction Steps

In 50 ml of ethanol was suspended 1.5 g (3.7 mmol) of 4-(6,7-dimethoxy-4-quinazolinyl)-N-(4-nitrophenyl)-1-piperazinecarboxamide obtained in Example 77, and a suspension of 500 mg of 10% palladium-carbon in 10 ml of water and 10 ml of ethanol was added thereto, followed by stirring in a stream of hydrogen at room temperature for 5 hours. After the catalyst was separated by filtration using Celite, the solvent was evaporated. Then, the residue was purified by silica gel chromatography and recrystallized from ethyl acetate to give the desired compound as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06750218B2
Source datasetuspto-grants-2004_06
ORD IDord-f7483eb7e12e4a77b06fad046cc2ab49
Source noteuspto-grants-2004_06