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HRID 266160Erstellt: 25. Oktober 2026
2-Pyridinamine, N-methyl- → ethyl 4-(3,4-dimethoxyphenyl)-6,7-dimethoxy-2-[N-methyl-N-(2-pyridyl)aminomethyl]quinoline-3-carboxylate
https://huagongshe.com/reaction/266160
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-Pyridinamine, N-methyl- | HCID 20727 | — |
| Edukt | Ethyl 2-chloromethyl-4-(3,4-dimethoxyphenyl)-6,7-dimethoxyquinoline-3-carboxylate | HCID 10813243 | — |
| Lösungsmittel | 2-Methoxyethanol | HCID 8019 | — |
| Produkt | ethyl 4-(3,4-dimethoxyphenyl)-6,7-dimethoxy-2-[N-methyl-N-(2-pyridyl)aminomethyl]quinoline-3-carboxylate | HCID 19032340 | 9% |
Reaktionsschritte
A mixture of ethyl 2-chloromethyl-4-(3,4-dimethoxyphenyl)-6,7-dimethoxyquinoline-3-carboxylate (1.0 g), 2-(methylamino)pyridine (0.95 g) and 2-methoxyethanol (30 ml) was stirred under reflux for 17 hours. The reaction mixture was concentrated under reduced pressure. Water was added to the residue, and the resulting mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to column chromatography on silica gel. The fractions eluted with hexane - ethyl acetate (3:2, v/v) gave ethyl 4-(3,4-dimethoxyphenyl)-6,7-dimethoxy-2-[N-methyl-N-(2-pyridyl)aminomethyl]quinoline-3-carboxylate (0.1 g, 9%). This compound was recrystallized from dichloromethane-ethanol. Pale yellow prisms, mp. 174°-175° 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-c6b16c641ff143efbe0a37014a7cb0db |
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| Quellennotiz | uspto-grants-1997_07 |
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