HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 266131Erstellt: 25. Oktober 2026
Piperazine → Ethyl 4-(3,4-dimethoxyphenyl)-6,7-dimethoxy-2-piperazinomethylquinoline-3-carboxylate
https://huagongshe.com/reaction/266131
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Piperazine | HCID 4837 | — |
| Edukt | Ethyl 2-chloromethyl-4-(3,4-dimethoxyphenyl)-6,7-dimethoxyquinoline-3-carboxylate | HCID 10813243 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | Ethyl 4-(3,4-dimethoxyphenyl)-6,7-dimethoxy-2-piperazinomethylquinoline-3-carboxylate | HCID 22097621 | 39% |
Reaktionsschritte
A mixture of ethyl 2-chloromethyl-4-(3,4-dimethoxyphenyl)-6,7-dimethoxyquinoline-3-carboxylate (1.0 g), piperazine (1.15 g) and methanol (15 ml) was stirred at room temperature for 36 hours. The reaction mixture was concentrated under reduced pressure, 6N hydrochloric acid (30 ml) was added to the residue, and the mixture was washed with dichloromethane. The aqueous layer was neutralized with 2N sodium hydroxide, and extracted with dichloromethane. The dichloromethane layer was washed with water and dried over magnesium sulfate, and the solvent was evaporated. The residual crystals were separated by filtration, and then recrystallized from dichloromethane-hexane to give ethyl 4-(3,4-dimethoxyphenyl)-6,7-dimethoxy-2-piperazinomethylquinoline-3-carboxylate (0.43 g, 39%). Colorless prisms, mp. 192°-193° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05650410 |
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| Quelldatensatz | uspto-grants-1997_07 |
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| ORD ID | ord-cca11ca634f94b93b1a5b714bb54b0f4 |
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| Quellennotiz | uspto-grants-1997_07 |
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