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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874834Generated: October 30, 2026

1-Methyl-1,4-cyclohexadiene → (R)-quinuclidin-3-yl((S)-phenyl(3-(piperidin-4-ylmethoxy)phenyl)methyl)carbamate

https://huagongshe.com/reaction/874834

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-1,4-cyclohexadieneHCID 78006—
Reactantbenzyl 4-((3-((5)-phenyl((((R)-quinuclidin-3-yloxy)carbonyl)-amino)methyl)phenoxy)methyl)piperidine-1-carboxylateHCID 90198097—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product(R)-quinuclidin-3-yl((S)-phenyl(3-(piperidin-4-ylmethoxy)phenyl)methyl)carbamateHCID 90210005103.3%

Reaction Steps

To a solution of benzyl 4-((3-((S)-phenyl((((R)-quinuclidin-3-yloxy)carbonyl)-amino)methyl)phenoxy)methyl)piperidine-1-carboxylate (1.32 g, 2.26 mmol) in ethanol (100 mL) was added palladium on charcoal (0.66 g) and stirred at room temperature for 10 minutes. 1-Methyl-1,4-cyclohexadiene (1.27 mL, 11.3 mmol) was added and the reaction mixture heated to reflux. The reaction mixture was stirred under reflux for 1 hour. The reaction mixture was allowed to cool and the suspension filtered. The filtrate was evaporated at reduced pressure to afford the title compound (1.05 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980913B2
Source datasetuspto-grants-2015_03
ORD IDord-77bbac0e13e0450b9ecb6b41af83b3ec
Source noteuspto-grants-2015_03