HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 280853Erstellt: 24. Oktober 2026
p-Anisoyl chloride → 1-[3-(4-Methoxybenzoylamino)propyl]-4-benzhydrylpiperazine
https://huagongshe.com/de/reaction/280853
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | p-Anisoyl chloride | HCID 7477 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 3-(4-Benzhydryl-1-piperazinyl)-1-propanamine | HCID 13767778 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | 1-[3-(4-Methoxybenzoylamino)propyl]-4-benzhydrylpiperazine | HCID 13362834 | 49,8% |
Reaktionsschritte
To a solution of 1-(3-aminopropyl)-4-benzhydrylpiperazine (1.55 g) and triethylamine (0.7 ml) in chloroform (15 ml) was dropwise added p-methoxybenzoyl chloride (0.85 g) at ambient temperature with stirring, which was continued for 20 minutes. The reaction mixture was washed successively with aqueous sodium bicarbonate and water. The organic layer was separated, dried and evaporated in vacuo. The resultant oily product was subjected to column chromatography on silica gel eluting with ethyl acetate. The fractions containing the desired compound were combined and evaporated in vacuo. The residue was crystallized from a mixture of ethyl acetate and hexane to give 1-[3-(4-methoxybenzoylamino)propyl]-4-benzhydrylpiperazine (1.1 g) as white crystals. mp: 126°-128° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04591590 |
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| Quelldatensatz | uspto-grants-1986_05 |
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| ORD ID | ord-45435e028d2149abb3c42f25079f2be1 |
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| Quellennotiz | uspto-grants-1986_05 |
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