HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1038432Erstellt: 26. Oktober 2026
N-(3-Aminophenyl)methanesulfamide → N-(3-((5-(4-(trifluoromethyl)phenyl)oxazol-2-yl)amino)phenyl) methane sulfonamide
https://huagongshe.com/reaction/1038432
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N-(3-Aminophenyl)methanesulfamide | HCID 2734262 | — |
| Edukt | 2-Chloro-5-(4-(trifluoromethyl)phenyl)oxazole | HCID 71060395 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Produkt | N-(3-((5-(4-(trifluoromethyl)phenyl)oxazol-2-yl)amino)phenyl) methane sulfonamide | HCID 71060442 | 41% |
Reaktionsschritte
A mixture of 2-chloro-5-(4-(trifluoromethyl)phenyl)oxazole 31 (0.599 g, 2.42 mmol) and commercially available N-(3-aminophenyl)methanesulfonamide 6 (0.451 g, 2.42 mmol) in 2-propanol (20 mL) was heated to 80° C. for 14 h with stirring. Upon cooling, solvent was evaporated and silica column purified (Biotage) (Acetone/hexane as an eluent) to provide N-(3-((5-(4-(trifluoromethyl)phenyl)oxazol-2-yl)amino)phenyl)methane sulfonamide 33 (0.393 g, 41% yield) as a solid. MS (ES) m/z 398 (M+H+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08551992B2 |
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| Quelldatensatz | uspto-grants-2013_10 |
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| ORD ID | ord-e7b07f2be1c64063b0de59860e8eb243 |
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| Quellennotiz | uspto-grants-2013_10 |
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