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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018988Generated: October 31, 2026

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

https://huagongshe.com/reaction/1018988

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(1-Acetylpiperidin-4-yl)furo[3,2-c]pyridineHCID 18399729—
SolventHydrochloric AcidHCID 313—
Product4-(4-Piperidinyl)furo[3,2-c]pyridineHCID 18399775—

Reaction Steps

A solution of 2.7 g of the product obtained in Step D in 80 ml of HCl (4N) is heated at 100° C. for 12 hours and then cooled, washed with ether, and rendered basic to a pH of 10 by the addition of an aqueous sodium hydroxide solution. After extraction with dichloromethane, the organic phase is dried, filtered and then evaporated to dryness enabling the expected product to be obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06486171B2
Source datasetuspto-grants-2002_11
ORD IDord-1a40daa6276a4ceb915aa63c280c7240
Source noteuspto-grants-2002_11