HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 53622Erstellt: 23. Oktober 2026
Methyl iodide → 2-amino-6-(2,6-dichlorophenyl)-8-methyl-7H,8H-pyrido[2,3-d]pyrimidin-7-one
https://huagongshe.com/de/reaction/53622
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | HCID 178418283 | HCID 178418283 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2-amino-6-(2,6-dichlorophenyl)-8-methyl-7H,8H-pyrido[2,3-d]pyrimidin-7-one | HCID 5327864 | 49,1% |
Reaktionsschritte
To a mixture of 2-amino-6-(2,6-dichlorophenyl)pyrido[2,3-d]pyrimidin-7-ol (3.7 g) from Example 11 in dimethylformamide was added NaH (50% suspension in mineral oil, 0.64 g). The resulting slurry was heated at 65° C. for 0.5 hour until a solution formed. It was then cooled to 50° C. and a solution of methyl iodide (2.0 g) in dimethylformamide (10 mL) was added dropwise to the reaction. The reaction mixture was warmed and kept between 60° C.-80° C. for 3 hours. Upon cooling to room temperature, the reaction mixture was poured into ice water. The insoluble white product was filtered, washed with water, and recrystallized from ethanol using charcoal to give 1.9 g of 2-amino-6-(2,6-dichlorophenyl)-8-methyl-pyrido[2,3 -d]pyrimidin-7(8H)-one, mp 235°-237° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05620981 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-5b94812b2cb04f379c12b9c616eef059 |
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| Quellennotiz | uspto-grants-1997_04 |
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