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HRID 32161Erstellt: 24. Oktober 2026

Potassium Phosphate, Tribasic → (R)-1-butyl-4-[2-(4,4-dimethylcyclohexyl)-4-(3-methoxypiperidin-1-yl)phenyl]piperazine

https://huagongshe.com/de/reaction/32161

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium Phosphate, TribasicHCID 62657—
EduktTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
Edukt1-[4-Bromo-2-(4,4-dimethylcyclohexyl)phenyl]-4-butylpiperazineHCID 23141738—
Edukt(3R)-3-methoxypiperidine hydrochlorideHCID 69216666—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelO-XyleneHCID 7237—
Produkt(R)-1-butyl-4-[2-(4,4-dimethylcyclohexyl)-4-(3-methoxypiperidin-1-yl)phenyl]piperazineHCID 5976938559,2%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 1-[4-bromo-2-(4,4-dimethylcyclohexyl)phenyl]-4-butylpiperazine (37.4 mg, 0.0918 mmol) produced in Example (21c), (R)-3-methoxypiperidine hydrochloride (16.7 mg, 0.110 mmol) produced in Example (49a), tripotassium phosphate (170 mg, 0.801 mmol), palladium(II) acetate (8.2 mg, 0.0365 mmol), tri-t-butylphosphonium tetrafluoroborate (32 mg, 0.110 mmol) and xylene (1.5 mL) was stirred for 4 hours and 30 minutes at an external temperature of 100° C. under a nitrogen atmosphere. The mixture was air-cooled to room temperature and then purified by NH silica gel column chromatography (ethyl acetate/hexane) to give 24 mg of (R)-1-butyl-4-[2-(4,4-dimethylcyclohexyl)-4-(3-methoxypiperidin-1-yl)phenyl]piperazine as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07425554B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-1059d9599d9f45f89d302d12e19044cb
Quellennotizuspto-grants-2008_09