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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609111Generated: October 30, 2026

Ammonium formate → 1-(9,10-Dihydro-9,10-methanoanthracen-9-ylmethyl)-4-(3-pyridylmethyl)piperidine

https://huagongshe.com/reaction/1609111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant1-[1-(9,10-Dihydro-9,10-methanoanthracen-9-ylmethyl)4-piperidyl]-1-(3-pyridyl)methanol acetateHCID 23185092—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product1-(9,10-Dihydro-9,10-methanoanthracen-9-ylmethyl)-4-(3-pyridylmethyl)piperidineHCID 1969868866%

Reaction Steps

A solution of 1-[1-(9,10-dihydro-9,10-methanoanthracen-9-ylmethyl)4-piperidyl]-1-(3-pyridyl)methanol acetate, prepared as in Example 53, (175 mg, 0.40 mmol), ammonium formate (175 mg, 2.78 mmol), and 10% palladium on carbon (175 mg) were heated to reflux in methanol (6 mL) under nitrogen (g) for 8 h. Additional ammonium formate (175 mg, 2.78 mmol) was added and heating was continued for an additional 8 h. The suspension was filtered through celite and the solids were washed thoroughly with methanol and ethyl acetate. Concentration of the filtrate left an off white foam. Flash chromatography on silica using 3% methanol/dichloromethane gave the title compound as a colorless glass (100mg, 0.26 mmol, 66%). This was dissolved in methanolic hydrogen chloride and concentrated from methanol (3×100 mL) to give the hydrochloride salt, mp 183°-185° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05399568
Source datasetuspto-grants-1995_03
ORD IDord-b1769b8dbbc9496dbaafc3156a9b67b0
Source noteuspto-grants-1995_03