HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1016642Erstellt: 25. Oktober 2026
Water → 6-Methyl-2-(4-methylphenyl)imidazo(1,2-a)pyridine
https://huagongshe.com/reaction/1016642
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 2-Amino-5-methylpyridine | HCID 15348 | — |
| Edukt | 2-Bromo-4'-methylacetophenone | HCID 69272 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 6-Methyl-2-(4-methylphenyl)imidazo(1,2-a)pyridine | HCID 667720 | 86% |
Reaktionsschritte
A solution of 2-bromo-1-(4-methylphenyl)ethanone (99.3 g, 0.47 mol) in dimethylformamide (250 mL) was added slowly to a solution of 5-methyl-2-pyridinamine (50.4 g, 0.47 mol) in dimethylformamide (250 mL). Sodium hydrogen carbonate (78.3 g, 0.93 mol) was added in portions and the mixture was stirred at room temperature for 15 min., then under reflux for 1.5 h. The mixture was cooled and poured into water (2500 mL). The solid was collected, washed with water (1000 mL) and recrystallised from dimethylformamide (400 mL). The solid was collected and dried in vacuo at 120° C. to give the title compound (89 g, 86%). 1H NMR (360 MHz, DMSO-d6) δ 8.30 (1H, d, J 1.5 Hz), 8.23 (1H, s), 7.84 (2H, d, J 8.0 Hz), 7.47 (1H, d, J 9.2 Hz), 7.25 (2H, d, J 8.0 Hz), 7.09 (1H, dd, J 9.2, 1.5 Hz), 2.33 (3H, s), and 2.28 (3H, s).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06476045B2 |
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| Quelldatensatz | uspto-grants-2002_11 |
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| ORD ID | ord-e8d4952219b74732a4bd9df57ceef865 |
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| Quellennotiz | uspto-grants-2002_11 |
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