Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Cesium carbonate | HCID 10796 | — |
| Edukt | 5-Chloro-1,10-phenanthroline | HCID 77865 | — |
| Edukt | 5-Bromo-2-(trifluoromethyl)pyridine | HCID 2761197 | — |
| Edukt | Water ammonium hydroxide | HCID 86589665 | — |
| Edukt | N-1,3-thiazol-2-ylpyrrolidine-1-carboxamide | HCID 86631924 | — |
| Lösungsmittel | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Produkt | HCID 87447416 | HCID 87447416 | — |
Reaktionsschritte
In a 4 mL vial charged with a stir bar, N-1,3-thiazol-2-ylpyrrolidine-1-carboxamide (46 mg, 0.23 mmol, Example 32A) was added, followed by copper(I) trifluoromethanesulfonate benzene complex (30 mg, 0.05 mmol), 5-chloro-1,10-phenanthroline (23 mg, 0.09 mmol) and cesium carbonate (100 mg, 0.3 mmol). A loose cap with septum was placed on the vial and the vial was placed under vacuum in a vacuum oven for 30 minutes. The solid mixture was purged with nitrogen gas a couple of times. Then 5-bromo-2-(trifluoromethyl)pyridine (68 mg, 0.3 mmol) dissolved in 1-methyl-2-pyrrolidinone (1.0 mL) was added to the solid mixture. The vial was capped and placed on a heater/stirrer and heated to 120° C. overnight. Then a 1 mL solution of concentrated ammonium hydroxide/water (1:2) was added. The reaction was filtered and concentrated to dryness. The residue was purified by reverse phase HPLC (C18, gradient 10-95% acetonitrile/water/0.1% trifluoroacetic acid) to provide the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08383657B2 |
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| Quelldatensatz | uspto-grants-2013_02 |
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| ORD ID | ord-56378088470641529a5f4944003f1830 |
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| Quellennotiz | uspto-grants-2013_02 |
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