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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 355751Erstellt: 25. Oktober 2026

Toluene → N-(4-Methoxy-3-(4-methyl-1-piperazinyl)phenyl)-4-cyclohexylbenzamide

https://huagongshe.com/reaction/355751

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktThionyl ChlorideHCID 24386—
Edukt4-Cyclohexylbenzoic acidHCID 88337—
Edukt4-Methoxy-3-(4-methylpiperazin-1-yl)anilineHCID 10331101—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTriethylamineHCID 8471—
ProduktN-(4-Methoxy-3-(4-methyl-1-piperazinyl)phenyl)-4-cyclohexylbenzamideHCID 1894067492%

Reaktionsschritte

4-Cyclohexylbenzoic acid (300 mg, 1.5 mmol) was heated at reflux with thionyl chloride (2 ml) and toluene (40 ml) for 2 h, and then evaporated to dryness under reduced pressure. 4-Methoxy-3-(4-methyl-1-piperazinyl)phenylamine (325 mg, 1.5 mmol) in dry dichloromethane (40 ml) was added with triethylamine (2 ml) and the mixture stirred for 1 h. The solution was partitioned between dichloromethane (40 ml) and saturated aqueous potassium carbonate (40 ml), the organic solution dried (sodium sulphate) and evaporated to dryness under reduced pressure to afford an oil, which was purified by flash column chromatography (silica, chloroform/methanol 5%) to afford the title compound (561 mg, 92%) which was crystallised from methanol/diethyl ether as the oxalate salt m.p. 117°-119° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05834471
Quelldatensatzuspto-grants-1998_11
ORD IDord-b49adb1682b84888bb73f304ad919862
Quellennotizuspto-grants-1998_11