HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 50191Erstellt: 24. Oktober 2026
Imidazolate → Methyl 5-[2-(4-cyanophenyl)ethylcarbonylamino]-6-methylamino-nicotinate
https://huagongshe.com/de/reaction/50191
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Imidazolate | HCID 3386966 | — |
| Edukt | 3-(4-Cyanophenyl)-propionic acid | HCID 9361742 | — |
| Edukt | Methyl 5-amino-6-(methylamino)pyridine-3-carboxylate | HCID 18412673 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Methyl 5-[2-(4-cyanophenyl)ethylcarbonylamino]-6-methylamino-nicotinate | HCID 18412623 | — |
Reaktionsschritte
A solution of 2.6 g (15 mmol) of 3-(4-cyanophenyl)propionic acid in 25 mL of absolute tetrahydrofuran was mixed with 2.4 g (15 mmol) of N,N′-carbonyldiimidazole and stirred for 20 minutes at room temperature. Then the imidazolide was mixed with a solution of 2.3 g (13 mmol) of methyl 5-amino-6-methylaminonicotinate in 25 mL of dimethyfformamide and heated for 3 hours to 100° C. After the removal of the solvent in vacuo, the crude product obtained was taken up in ethyl acetate, the organic phase was washed with water and after drying over sodium sulfate it was again freed from solvent. The residue obtained was purified by flash chromatography (silica gel; gradient: dichloromethane to dichloromethane/ethanol=19:1). Yield: 2.1 g (50% of theory) of beige solid; Rf value: 0.54 (silica gel; ethyl acetate/ethanol/ammonia=90:10:1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06710055B2 |
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| Quelldatensatz | uspto-grants-2004_03 |
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| ORD ID | ord-8ed547a2fc2a4ce58ab475f72df20328 |
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| Quellennotiz | uspto-grants-2004_03 |
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