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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184803Generated: October 31, 2026

Ammonium formate → 4-(1-Acetylpiperidin-4-yl)furo[3,2-c]pyridine

https://huagongshe.com/reaction/2184803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant4-(1-Acetyl-1,2,3,6-tetrahydropyridin-4-yl)furo[3,2-c]pyridineHCID 18399776—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-(1-Acetylpiperidin-4-yl)furo[3,2-c]pyridineHCID 18399729—

Reaction Steps

0.7 g of Pd/C (10%) is added to a solution of 3.4 g of the product obtained in Step C and 4.4 g of ammonium formate in 150 ml of anhydrous methanol under a stream of argon. After refluxing for 45 minutes, the reaction mixture is cooled, 4.4 g of ammonium formate 5 and 0.2 g of Pd/C (10%) are added, and the reaction mixture is then heated at reflux for 30 minutes. After returning to ambient temperature, filtration over Celite and concentration under reduced pressure, the residue is taken up in water and then extracted with dichloromethane. The expected product is isolated by extraction, drying, filtration and concentration under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06399616B1
Source datasetuspto-grants-2002_06
ORD IDord-ea629e2966e64f38bae43c969242f85d
Source noteuspto-grants-2002_06