Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Hydrazine | HCID 9321 | — |
| Edukt | 2-Acetylthiazole | HCID 520108 | — |
| Edukt | N,N-dimethylformamide N,N-dimethylacetamide | HCID 22628260 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2-(1H-pyrazol-3-yl)-1,3-thiazole | HCID 3363559 | 100% |
Reaktionsschritte
Dissolved 1-(thiazol-2-yl)ethanone (1-BA-1, 5 g, 39.7 mmole) in DMF DMA (9.5 g, 2 eq). The resulting mixture was warmed to 100° C. until all the ketone starting material was consumed. This material was concentrated under reduced pressure to give 6.5 g of crude intermediate. This material was dissolved in 25 mL of DCM and 5 mL of HOAc was added, followed by hydrazine (5 g, 4 eq) at 0° C. The resulting mixture was heated at reflux until all the starting material was consumed. The reaction mixture was cooled to rt and neutralized with 30 mL of a saturated NaHCO3 solution. The layers were separated and the aqueous layer was extracted with DCM (2×50 mL). The organic layers were dried over MgSO4, filtered, and concentrated under reduced pressure. The crude material was purified by MPLC (eluted with 0-20% MeOH/DCM) to give 2-(1H-pyrazol-5-yl)thiazole (Compound 2-BA-1, ˜6 g). LC/MS: 152.0 m/z (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08541418B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-33c7b881441d4f7ba523444091fcca09 |
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| Quellennotiz | uspto-grants-2013_09 |
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