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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353138Generated: October 29, 2026

HCID 22707433, compound → HCID 22707738, compound

https://huagongshe.com/reaction/353138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22707433HCID 22707433—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 22707738HCID 2270773845%

Reaction Steps

To a solution of 455.6 mg (0.97 mmol) of 4-(7-nitro-4-quinazolinyl)-N-(4-phenoxyphenyl)-1-piperazinecarboxamide obtained in Example 322 in 10 ml of ethanol was added a suspension of 100 mg of 10% palladium-carbon in 5 ml of ethanol and 2 ml of water, followed by stirring in a stream of hydrogen at room temperature for 4 hours. After the catalyst was separated by filtration using Celite, the solvent was evaporated. The residue was purified by silica gel chromatography 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-b4aadf4c14584f28b5fbfa79e127c78e
Source noteuspto-grants-2004_06