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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238661Generated: November 2, 2026

HCID 68686560, compound → HCID 68688595, compound

https://huagongshe.com/reaction/2238661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68686560HCID 68686560—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68688595HCID 6868859518.1%

Reaction Steps

83 mg of the 4-[8-(difluoromethyl)imidazo[1,2-a]pyridin-3-yl]-2-{[(1S)-1-(4-nitrophenyl)ethyl]amino}pyrimidine-5-carbonitrile [103-1] was dissolved in a mixture solvent of 2 mL of ethanol and 3 mL of tetrahydrofuran, then 40 mg of 10% palladiumcarbon catalyst was added, and stirred overnight at room temperature in a hydrogen atmosphere. The insolubles were filtered through celite and the filtrate was concentrated under reduced pressure to obtain a residue. The residue was purified by preparative thin-layer chromatography, and 14 mg of 2-{[(1S)-1-(4-aminophenyl)ethyl]amino}-4-[8-(difluoromethyl)imidazo[1,2-a]pyridin-3-yl]pyrimidin-5-carbonitrile [103-2] was obtained as pale yellow amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718801B2
Source datasetuspto-grants-2010_05
ORD IDord-b35a96a3d855460e8d115b8b2be381b6
Source noteuspto-grants-2010_05