HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1473287Erstellt: 26. Oktober 2026
Dichloromethane → 5-(2-Bromo-4-(trifluoromethyl)phenyl)-N-(1,2,4-thiadiazol-5-YL)naphthalene-2-sulfonamide
https://huagongshe.com/reaction/1473287
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | Trifluoroacetic acid | HCID 6422 | — |
| Edukt | 5-(2-bromo-4-(trifluoromethyl)phenyl)-N-(2,4-dimethoxybenzyl)-N-(1,2,4-thiadiazol-5-yl)naphthalene-2-sulfonamide | HCID 86687342 | — |
| Produkt | 5-(2-Bromo-4-(trifluoromethyl)phenyl)-N-(1,2,4-thiadiazol-5-YL)naphthalene-2-sulfonamide | HCID 86687346 | — |
Reaktionsschritte
To a solution of 5-(2-bromo-4-(trifluoromethyl)phenyl)-N-(2,4-dimethoxybenzyl)-N-(1,2,4-thiadiazol-5-yl)naphthalene-2-sulfonamide (3.27 g, 4.92 mmol) in DCM (49.2 mL, 4.92 mmol) was added TFA (1.896 mL, 24.60 mmol). The resulting mixture was stirred at room temperature. After 30 min, LC/MS showed mainly desired product. The mixture was stirred for an additional hour at room temperature until the reaction was complete. The mixture was partially concentrated until a white solid crashed out. The solid was filtered, washed with diethyl ether and dried to afford 5-(2-bromo-4-(trifluoromethyl)phenyl)-N-(1,2,4-thiadiazol-5-yl)naphthalene-2-sulfonamide (2.4 g, 4.67 mmol). 1H NMR (500 MHz, DMSO-d6) δ ppm 7.58 (d, J=8.76 Hz, 1H) 7.68-7.74 (m, 1H) 7.74-7.83 (m, 2H) 7.87 (d, J=8.01 Hz, 1H) 8.16-8.24 (m, 2H) 8.34 (d, J=8.34 Hz, 1H) 8.52-8.57 (m, 2H); m/z (ESI) 513.7 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09012443B2 |
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| Quelldatensatz | uspto-grants-2015_04 |
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| ORD ID | ord-f217003fd2bb4baf80d0b1a9e58f2860 |
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| Quellennotiz | uspto-grants-2015_04 |
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