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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010898Generated: October 30, 2026

HCID 67313255, compound → HCID 67314727, compound

https://huagongshe.com/reaction/1010898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67313255HCID 67313255—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67314727HCID 6731472736.5%

Reaction Steps

21 mg of the compound [17-1] was dissolved in a mixed solvent of 3 mL of tetrahydrofuran and 3 mL of methanol, then 20 mg of a carbon catalyst of 20% palladium hydroxide was added thereto, and the mixture was stirred for 2 hours at room temperature under hydrogen atmosphere. The catalyst was filtered through celite, and the filtrate was concentrated under reduced pressure. Diethylether was added to the resulting residue, and thus produced solid was taken by filtration to obtain 6 mg of 2-({(1S)-1-[4-(1-hydroxy-2-piperidin-4-ylethyl)phenyl]ethyl}amino)-4-(8-methylimidazo[1,2-a]pyridin-3-yl)pyrimidine-5-carbonitrile [17-2] (hereinafter, referred to as the compound [17-2]).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977336B2
Source datasetuspto-grants-2011_07
ORD IDord-c444c0123c52409d8940ce770051258f
Source noteuspto-grants-2011_07