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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018987Generated: October 30, 2026

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

https://huagongshe.com/reaction/1018987

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 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 numberUS06486171B2
Source datasetuspto-grants-2002_11
ORD IDord-b0a5f0e040c14630a5e0b2bf9cefc1c3
Source noteuspto-grants-2002_11