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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340416Generated: October 30, 2026

Triphenylphosphine → Tert-butyl 4-(6-(1-(4-(trifluoromethyl)phenyl)piperidin-4-yloxy)quinoline-3-carboxamido)piperidine-1-carboxylate

https://huagongshe.com/reaction/340416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant1-[4-(Trifluoromethyl)phenyl]piperidin-4-olHCID 22097674—
ReactantTert-butyl 4-(6-hydroxyquinoline-3-carboxamido)piperidine-1-carboxylateHCID 57750083—
SolventTolueneHCID 1140—
ProductTert-butyl 4-(6-(1-(4-(trifluoromethyl)phenyl)piperidin-4-yloxy)quinoline-3-carboxamido)piperidine-1-carboxylateHCID 4417708127%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred suspension of the product of step 2 above (0.7 g, 1.88 mmol) in toluene (15 mL) at room temperature was added diisopropyl azodicarboxylate (557 μl, 2.83 mmol), 1-(4-(trifluoromethyl)phenyl)piperidin-4-ol (0.693 g, 2.83 mmol), and triphenyl phosphine (0.742 g, 2.83 mmol). The mixture was stirred at 50° C. overnight and then concentrated under reduced pressure. The residue was purified by flash chromatography (silica gel, 3% methanol in methylene chloride) to afford tert-butyl 4-(6-(1-(4-(trifluoromethyl)phenyl)piperidin-4-yloxy)quinoline-3-carboxamido)piperidine-1-carboxylate as a white solid (0.306 g, 27%). LCMS (m/z): 599 (MH+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895578B2
Source datasetuspto-grants-2014_11
ORD IDord-72f51beebea44866883dcbe731a02df0
Source noteuspto-grants-2014_11