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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1675146Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1675146

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
EduktDiisopropyl azodicarboxylateHCID 5363146—
Edukt4-Piperidin-4-ylphenolHCID 10511511—
Edukt2-(1-methyl-1H-pyrazol-5-yl)ethan-1-olHCID 21832419—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-[4-[2-(1-methyl-1H-pyrazol-5-yl)ethoxy]phenyl]piperidineHCID 6734030899,3%

Reaktionsbedingungen

Temperatur22 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08003649B2
Quelldatensatzuspto-grants-2011_08
ORD IDord-64bc66898c944875a16910785de0ea9b
Quellennotizuspto-grants-2011_08