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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675146Generated: October 26, 2026

Triphenylphosphine → 4-[4-[2-(1-methyl-1H-pyrazol-5-yl)ethoxy]phenyl]piperidine

https://huagongshe.com/reaction/1675146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactant4-Piperidin-4-ylphenolHCID 10511511—
Reactant2-(1-methyl-1H-pyrazol-5-yl)ethan-1-olHCID 21832419—
SolventDichloromethaneHCID 6344—
Product4-[4-[2-(1-methyl-1H-pyrazol-5-yl)ethoxy]phenyl]piperidineHCID 6734030899.3%

Reaction Conditions

Temperature22 °C

Reaction Steps

DIAD (64.8 μl, 0.33 mmol) was added to 4-(piperidin-4-yl)phenol (CAS 263139-27-1, 53 mg, 0.30 mmol), 2-(1-methyl-1H-pyrazol-5-yl)ethanol (obtained as described in PCT Int. Appl. WO 2007017222, Intermediate 1) (37.7 mg, 0.30 mmol) and triphenylphosphine (86 mg, 0.33 mmol) in DCM (3 mL) at 20° C. under nitrogen. The resulting mixture was stirred at 22° C. for 3 days. The reaction mixture was purified by ion exchange chromatography, using an SCX column. The desired product was eluted from the column using 7M ammonia in methanol and pure fractions were evaporated to dryness to afford 4-[4-[2-(1-methyl-1H-pyrazol-5-yl)ethoxy]phenyl]piperidine (85 mg, 96%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003649B2
Source datasetuspto-grants-2011_08
ORD IDord-64bc66898c944875a16910785de0ea9b
Source noteuspto-grants-2011_08