Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010902Generated: October 29, 2026

HCID 67314324, compound → HCID 67313969, compound

https://huagongshe.com/reaction/1010902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67314324HCID 67314324—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
ProductHCID 67313969HCID 6731396971.5%

Reaction Steps

118 mg of the compound [25-2] was dissolved in 4 mL of ethanol, then 50 mg of a carbon catalyst of 20% palladium hydroxide was added thereto, and the mixture was stirred overnight at room temperature under hydrogen atmosphere. The catalyst was filtered through celite, the filtrate was concentrated under reduced pressure, and then the resulting residue was purified by preparative thin-layer chromatography, to obtain 66 mg of 4-(8-ethylimidazo[1,2-a]pyridin-3-yl)-2-[((1S)-1-{4-[hydroxy(piperidin-4-yl)methyl]phenyl}ethyl)amino]pyrimidine-5-carbonitrile [25-3] (hereinafter, referred to as the compound [25-3]).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977336B2
Source datasetuspto-grants-2011_07
ORD IDord-320f806d193743b391383f63318e8aa8
Source noteuspto-grants-2011_07