HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 33963Erstellt: 24. Oktober 2026
Dimethylformamide → 3-methyl-2-methylsulfanyl-5-naphthalen-2-yl-6-pyridin-4-yl-3H-pyrimidin-4-one
https://huagongshe.com/de/reaction/33963
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | 4-Cyanopyridine | HCID 7506 | — |
| Edukt | Ethyl 2-naphthylacetate | HCID 256821 | — |
| Edukt | Methylthioisocyanate | HCID 21933440 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Produkt | 3-methyl-2-methylsulfanyl-5-naphthalen-2-yl-6-pyridin-4-yl-3H-pyrimidin-4-one | HCID 22346641 | — |
Reaktionsschritte
To a stirring solution of ethyl-2-naphthylacetate (10.0 g, 46.7 mmol) and 4-cyanopyridine (4.86 g, 46.7 mmol) in 50 mL dry dimethylformamide (DMF) at room temperature under nitrogen was added 47 mL potassium tert-butoxide (1.0 M in 2-methyl-2-propanol) dropwise via syringe. The dark red solution was stirred at room temperature for 75 min. Methylthioisocyanate (3.41 g, 46.7 mmol) in 10 mL DMF added whole. The solution was stirred for 90 min at room temperature. Iodomethane (2.95 mL, 46.7 mmol) was added dropwise over a 3 min period. Solid precipitates out of reaction. Continued to stir as a mixture for 30 min. Water (500 mL) was slowly added to reaction mixture. The solid was collected via filtration then washed with water, cold ethanol (50 mL), and ether. The solid was air dried for 3 days. M+1=360.2.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07429594B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-77270c2e721440a28b95e897fee0bb01 |
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| Quellennotiz | uspto-grants-2008_09 |
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