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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872540Generated: November 1, 2026

4'-chlorospiro[1-azabicyclo[2.2.2]octane-3,2'(3'H)-furo[3,2-c]pyridine] → Spiro[1-azabicyclo[2.2.2]octane-3,2'(3'H)-furo[3,2-c]pyrdine]

https://huagongshe.com/reaction/1872540

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-chlorospiro[1-azabicyclo[2.2.2]octane-3,2'(3'H)-furo[3,2-c]pyridine]HCID 22045869—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductSpiro[1-azabicyclo[2.2.2]octane-3,2'(3'H)-furo[3,2-c]pyrdine]HCID 22045857104%

Reaction Steps

The 4'-chlorospiro[1-azabicyclo[2.2.2]octane-3,2'(3'H)-furo[3,2-c]pyridine] (125 mg or 5.0 mmol) from Example 33 was dissolved in 50 mL of anhydrous methanol, and 25 mg of 10% palladium on carbon was added. The bottle was placed on the Parr apparatus under hydrogen atmosphere and shaken for 2.5 hours. The Pd/C was removed by filtration and washed with methanol. The solvent was removed in vacuo and the residue was taken up in chloroform and methanol and transferred to a vial. The solvent was removed in vacuo and chased with two portions of ether. After drying with high vacuum obtained 112 mg of off-white powder (104% with residual solvent.) Electrospray MS 217 [MH]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06110914
Source datasetuspto-grants-2000_08
ORD IDord-638556a43f494c68b8ddae6a4958a351
Source noteuspto-grants-2000_08