HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1068054Erstellt: 27. Oktober 2026
Sodium Hydroxide → N-[(4-bromophenyl)methyl]-1-morpholino-6-(morpholinomethyl)-4-oxo-quinoline-3-carboxamide
https://huagongshe.com/reaction/1068054
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 4-Bromobenzylamine hydrochloride | HCID 2724096 | — |
| Edukt | Ethyl 1-(4-morpholinyl)-6-(4-morpholinylmethyl)-4-oxo-1,4-dihydro-3-quinolinecarboxylate | HCID 21192510 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | N-[(4-bromophenyl)methyl]-1-morpholino-6-(morpholinomethyl)-4-oxo-quinoline-3-carboxamide | HCID 490489 | 68% |
Reaktionsschritte
4-Bromobenzylamine hydrochloride (2.22 g) is suspended in water (5 mL) and neutralized with 2N aqueous NaOH (5 mL). The free amine is extracted with dichloromethane (2×25 mL). The organic layers are combined, washed with brine (5 mL), and dried with Na2SO4. The solution is concentrated in vacuo to afford 1.48 g of a clear, colorless oil which is then combined with ethyl 1-(4-morpholinyl)-6-(4-morpholinylmethyl)-4-oxo-1,4-dihydro-3-quinolinecarboxylate (0.48 g) from Preparation No. 56 and heated to 190° C. for 3 hours. The reaction mixture is allowed to cool to room temperature, and the resulting solid is recrystallized in ethyl acetate to afford 0.44 g of the title compound as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06248739B1 |
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| Quelldatensatz | uspto-grants-2001_06 |
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| ORD ID | ord-e40cb64c7f374a5ea9db5bbe926592f0 |
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| Quellennotiz | uspto-grants-2001_06 |
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