HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1035801Erstellt: 25. Oktober 2026
N-(3-Aminophenyl)-1-phenylmethanesulfonamide → N-(3-((5-(4-cyanophenyl)oxazol-2-yl)amino)phenyl)-1-phenylmethanesulfonamide
https://huagongshe.com/reaction/1035801
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | N-(3-Aminophenyl)-1-phenylmethanesulfonamide | HCID 16772451 | — |
| Edukt | 4-(2-Chlorooxazol-5-yl)benzonitrile | HCID 68443558 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Produkt | N-(3-((5-(4-cyanophenyl)oxazol-2-yl)amino)phenyl)-1-phenylmethanesulfonamide | HCID 71060644 | — |
Reaktionsschritte
A mixture of 4-(2-chlorooxazol-5-yl)benzonitrile 2 (0.20 g, 0.98 mmol) and N-(3-aminophenyl)-1-phenylmethanesulfonamide 4 (0.256 g, 0.98 mmol) in 2-propanol (20 mL) was heated to 80° C. for 18 h with stirring. Upon cooling, a white solid precipitated out which was filtered off, washed with 2-propanol, and dried. This was then triturated with ether and filtered to yield the title product, a white solid, as the hydrochloride salt of 5 (0.15 g, 36%). Free amine containing filtrate was evaporated and silica column purified (Biotage) (Acetone/hexane as an eluent) to provide 5 (0.15 g, 36% yield) as pale yellow solid. MS (ES) m/z 431 (M+H+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08546400B2 |
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| Quelldatensatz | uspto-grants-2013_10 |
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| ORD ID | ord-204916e8562a43119e8fb060b8645f01 |
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| Quellennotiz | uspto-grants-2013_10 |
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