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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Toluene | HCID 1140 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Edukt | 4-Cyclohexylbenzoic acid | HCID 88337 | — |
| Edukt | 4-Methoxy-3-(4-methylpiperazin-1-yl)aniline | HCID 10331101 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | N-(4-Methoxy-3-(4-methyl-1-piperazinyl)phenyl)-4-cyclohexylbenzamide | HCID 18940674 | 92% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05834471 |
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| Quelldatensatz | uspto-grants-1998_11 |
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| ORD ID | ord-b49adb1682b84888bb73f304ad919862 |
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| Quellennotiz | uspto-grants-1998_11 |
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