Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 5-Methylpicolinonitrile | HCID 74183 | — |
| Edukt | 4-(Methylsulfonyl)aniline hydrochloride | HCID 2735180 | — |
| Edukt | Trimethylaluminum | HCID 16682925 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | HCID 178425635 | HCID 178425635 | — |
Reaktionsschritte
To a suspension of 4-(methylsulfonyl)aniline hydrochloride (10 mmol) in toluene (60 ml) at 0° C., trimethylaluminum (2M solution in toluene, 10 ml, 20 mmol) is added over 10 minutes. The reaction mixture is allowed to warm to room temperature and stirred for 2 hours. A solution of 5-methyl-2-cyanopyridine (20 mmol) in toluene (100 ml) is added over 10 minutes and the mixture is heated to 85°-90° C. After 24 hours, the reaction mixture is cooled to room temperature and poured over a slurry of silica gel in chloroform. After filtration, the residue is washed with a mixture of methylene chloride and methanol and later with methanol. The combined filtrates are concentrated and the resulting solid is stirred with a mixture of hexane and ethyl acetate (1000 ml) and filtered. The product obtained is used in the next reaction without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05616601 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-97885743dc534166b159a6f7c0e7f8fe |
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| Quellennotiz | uspto-grants-1997_04 |
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