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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1727136Erstellt: 24. Oktober 2026

Rolipram → 3-[4-(3-Cyclopentyloxy-4-methoxy-phenyl)-2-oxo-pyrrolidin-1-yl]benzonitrile

https://huagongshe.com/de/reaction/1727136

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktRolipramHCID 5092—
Edukt3-BromobenzonitrileHCID 23381—
Edukt1,2-Diaminocyclohexane, trans-HCID 43806—
EduktPotassium Phosphate, TribasicHCID 62657—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt3-[4-(3-Cyclopentyloxy-4-methoxy-phenyl)-2-oxo-pyrrolidin-1-yl]benzonitrileHCID 1047466996,2%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

A mixture of 4-(3-cyclopentyloxy-4-methoxyphenyl)-pyrrolidin-2-one (1.5 g, 5 mmol), 3-bromobenzonitrile (1.36 g, 7.5 mmol), potassium phosphate (1.9 g, 9.8 mmol), and 1,2-trans-cyclohexanediamine (60 μL) was created in a dry round bottom flask under nitrogen containing DMF (9 mL) and dioxane (9 mL). The mixture was stirred and CuI (100 mg) was added. The resulting reaction mixture was heated to 110° C. with stirring under N2 for 20 h, and then cooled to r.t. The mixture was diluted with EtOAc and then filtered. The filtrate was washed with saturated aqueous solutions of NH4Cl and brine, dried over MgSO4, and concentrated under reduced pressure. Chromatography on silica gel (EtOAc:hexane=1:3 to 1:1) gave 1.81 g of 3-[4-(3-cyclopentyloxy-4-methoxy-phenyl)-2-oxo-pyrrolidin-1-yl]benzonitrile. Yield: 90%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07495016B2
Quelldatensatzuspto-grants-2009_02
ORD IDord-d126f3eed8c14591a419ca2157fcb205
Quellennotizuspto-grants-2009_02