Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethyl Sulfoxide | HCID 679 | — |
| Edukt | 3-Fluoroisonicotinaldehyde | HCID 2763003 | — |
| Edukt | HCID 178507667 | HCID 178507667 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | HCID 68153707 | HCID 68153707 | 39,7% |
Reaktionsschritte
A mixture of 0.90 g of 3-amino-5-(trifluoromethyl)-pyridine-2-thiol, 0.58 g of 3-fluoroisonicotinaldehyde and 5 ml of DMSO was stirred at 170° C. for 2 hours. The reaction mixture was cooled down to room temperature, then, to the reaction mixture was added water, and the resultant mixture was extracted with ethyl acetate twice. The combined organic layers were washed with water and saturated saline, dried over magnesium sulfate, then, concentrated under reduced pressure. The residue was subjected to silica gel column chromatography, to obtain 0.55 g of 2-(3-fluoropyridin-4-yl)-6-(trifluoromethyl)thiazolo[5,4-b]pyridine (hereinafter, referred to as the present compound 9).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08742112B2 |
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| Quelldatensatz | uspto-grants-2014_06 |
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| ORD ID | ord-87cc4ce7d139499d83fb9c970dcfd567 |
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| Quellennotiz | uspto-grants-2014_06 |
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