Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 4-(Trifluoromethyl)phenyl isocyanate | HCID 73768 | — |
| Edukt | HCID 178507541 | HCID 178507541 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | HCID 178522056 | HCID 178522056 | 75% |
Reaktionsschritte
To 3-(4-Pyridin-4-yl-1H-pyrazol-3-yl)-phenylamine (700 mg, 3 mmol) in anhydrous pyridine (15 mL) at 0° C. 4-trifluoromethylphenylisocyanate (420 μL, 3 mmol) was added. The reaction was stirred for 2 hours at 0° C. under nitrogen atmosphere to give a mixture of monourea and bis-urea as regioisomeric mixture. Solvent was removed under reduced pressure. The residue was dissolved in methanol (15 mL) and triethylamine (1 mL, 7.8 mmol) was added and the reaction was stirred at room temperature overnight. After this time only the monourea could be detected by HPLC/MS. The solvent was removed under reduced pressure and the residue was dissolved in ethyl acetate (100 mL) and washed successively with water (3×50 mL). The crude was purified by silica gel column chromatography (DCM/methanol 9:1) to give the desired product as a white solid (75%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08541575B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-568357e338334b369eb32b7a7405ce38 |
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| Quellennotiz | uspto-grants-2013_09 |
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