HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1621785Erstellt: 26. Oktober 2026
HCID 86647061, Verbindung → N-(5-amino-2-chloropyridin-3-yl)-4-fluorobenzenesulfonamide
https://huagongshe.com/reaction/1621785
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | HCID 86647061 | HCID 86647061 | — |
| Lösungsmittel | Hydrochloric Acid | HCID 313 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | N-(5-amino-2-chloropyridin-3-yl)-4-fluorobenzenesulfonamide | HCID 71480919 | 80,2% |
Reaktionsschritte
A solution of N-(2-chloro-5-(diphenylmethyleneamino)pyridin-3-yl)-4-fluorobenzenesulfonamide (0.520 g, 1.116 mmol) in THF (8 mL) and hydrochloric acid, 2N (J. T. Baker) (0.837 mL, 1.674 mmol) was stirred at rt in a sealed tube for 30 min. The reaction mixture was partitioned between EtOAc and sat. NaHCO3. The aqueous layer was extracted with EtOAc (2×10 mL). The combined organic layers were dried over MgSO4 and concentrated. The crude product was purified by column chromatography (80 g, 20% to 40% acetone in hexanes) to give the product as a yellow solid (0.270 g). m/z (ESI, +ve ion) 302.0 (M+H)+. 1H NMR (300 MHz, CDCl3) δ 7.80 (dd, J=8.77, 4.97 Hz, 2H); 7.61 (d, J=2.63 Hz, 1H); 7.34 (d, J=2.48 Hz, 1H); 7.16 (t, J=8.48 Hz, 2H); 6.82 (br. s., 1H); 3.84 (br. s., 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08772480B2 |
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| Quelldatensatz | uspto-grants-2014_07 |
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| ORD ID | ord-df1b4696192842299d235ec8c83c52ce |
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| Quellennotiz | uspto-grants-2014_07 |
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