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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912754Generated: October 31, 2026

HCID 23155053, compound → HCID 23155220, compound

https://huagongshe.com/reaction/1912754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23155053HCID 23155053—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductHCID 23155220HCID 23155220—

Reaction Steps

In 20 mL of methanol, 33 mg (0.1237 mmol) of 1-(4-nitrophenyl)-1H-imidazo[4,5-c]pyridine prepared in Step A was dissolved and the solution was stirred on 5 mg of 10% palladium carbon in a hydrogen atmosphere at room temperature at normal pressures for one hour. After removal of the palladium carbon by filtration, the solvent was distilled under reduced pressure, and the obtained product was vacuum dried to obtain 4-(imidazo[4,5-c]-pyridin-1-yl)aniline as a white solid. This product was used in process C without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609656B2
Source datasetuspto-grants-2013_12
ORD IDord-995224077a1b424a9c6c9df482385450
Source noteuspto-grants-2013_12