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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088229Generated: October 26, 2026

(1R*,2R*,5R*)-8-Benzyl-2-{[3,5-bis(trifluoromethyl)phenyl]methoxy}-1-phenyl-8-azabicyclo[3.2.1]octane → (1R*,2R*,5R*)-2-{[3,5-bis(trifluoromethyl)phenyl]methoxy}-1-phenyl-8-azabicyclo[3.2.1]octane

https://huagongshe.com/reaction/2088229

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1R*,2R*,5R*)-8-Benzyl-2-{[3,5-bis(trifluoromethyl)phenyl]methoxy}-1-phenyl-8-azabicyclo[3.2.1]octaneHCID 86586691—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product(1R*,2R*,5R*)-2-{[3,5-bis(trifluoromethyl)phenyl]methoxy}-1-phenyl-8-azabicyclo[3.2.1]octaneHCID 8658664759%

Reaction Steps

A mixture of (1R,2R,5R)-8-benzyl-2-{[3,5-bis(trifluoromethyl)phenyl]methoxy}-1-phenyl-8-azabicyclo[3.2.1]octane (Example 180; 165 mg), 10% palladium on charcoal (215 mg) and ethanol (15 ml) was stirred under hydrogen atmosphere (1 atm) at +65° C. for 45 minutes. The reaction mixture was cooled to room temperature, flushed with nitrogen gas and filtered through a pad of Celite™. The filtrate was concentrated. The residue was purified by chromatography on silica gel (dichloromethane:methanol:ammonia) to give the title compound (64 mg, 59%). The hydrochloride salt of the title compound was prepared by treatment with ethereal HCl.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06727249B2
Source datasetuspto-grants-2004_04
ORD IDord-861a54b193b949a8a62446558a8a9268
Source noteuspto-grants-2004_04