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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425994Generated: October 30, 2026

Ammonium formate → HCID 57867990, compound

https://huagongshe.com/reaction/425994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant2-[(1-benzylpiperidin-4-yl)amino]-N-(1-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-7-yl)-4-(trifluoromethyl)benzamideHCID 66703828—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductHCID 57867990HCID 57867990—

Reaction Steps

Palladium-carbon and ammonium formate were added to a methanol solution of 2-[(1-benzylpiperidin-4-yl)amino]-N-(1-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-7-yl)-4-(trifluoromethyl)benzamide, followed by heating under reflux for 2 hours. After spontaneous cooling, Celite filtration was carried out and then the filtrate was concentrated under a reduced pressure. By purifying the residue by silica gel column chromatography, N-(1-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-7-yl)-2-(piperidin-4-ylamino)-4-(trifluoromethyl)benzamide was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106190B2
Source datasetuspto-grants-2012_01
ORD IDord-a48f162131e74623add66c301965ef07
Source noteuspto-grants-2012_01