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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1434582Erstellt: 25. Oktober 2026

Potassium Iodide → 1-(4-{4-[1-(2-Methoxy-ethyl)-piperidin-4-yloxy]-benzyl}-piperazin-1-yl)-1-phenyl-methanone

https://huagongshe.com/reaction/1434582

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktPotassium CarbonateHCID 11430—
Edukt2-Chloroethyl methyl etherHCID 12316—
EduktPhenyl[4-({4-[(piperidin-4-yl)oxy]phenyl}methyl)piperazin-1-yl]methanoneHCID 57935703—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelMethyl Ethyl KetoneHCID 6569—
Produkt1-(4-{4-[1-(2-Methoxy-ethyl)-piperidin-4-yloxy]-benzyl}-piperazin-1-yl)-1-phenyl-methanoneHCID 5793583343,4%

Reaktionsschritte

1-Phenyl-1-{4-[4-(piperidin-4-yloxy)-benzyl]-piperazin-1-yl}-methanone (E32) (150 mg, 0.40 mmol) was dissolved in 2-butanone and treated with 1-chloro-2-methoxy-ethane (0.08 ml, 0.80 mmol), potassium carbonate (132 mg, 0.96 mmol) and potassium iodide (159 mg, 0.96 mmol). The reaction mixture was heated under reflux for 24 hours. The mixture was allowed to cool to room temperature, acidified by the addition of glacial acetic acid and passed down an SCX ion exchange column (2 g) eluting with methanol followed by ammonia/methanol (1:9). The basic fractions were combined and concentrated in vacuo to afford the title compound (76 mg). MS(ES+) m/e 438 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07615550B2
Quelldatensatzuspto-grants-2009_11
ORD IDord-9e5daa4c88af4dbf984dd9b2111517fb
Quellennotizuspto-grants-2009_11