HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
3-Iodophenylisothiocyanate → HCID 57773569, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 3-Iodophenylisothiocyanate | HCID 151083 | — |
| Edukt | 4-(3-(4-Aminophenyl)thioureido)benzenesulfonamide | HCID 57773595 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | HCID 57773569 | HCID 57773569 | 78% |
Reaktionsschritte
To a solution of 4-(3-(4-aminophenyl)thioureido)benzenesulfonamide (0.322 g, 1.0 mmol) in acetonitrile was added 1-iodo-3-isothiocyanatobenzene (0.261 g, 1.0 mmol). The mixture was stirred at room temperature overnight. The solvent was evaporated under reduced pressure and water was added into the crude reaction mixture. The precipitate which formed was filtered, and dried to afford the title product as a white solid (0.452 g, 78%). 1H NMR (400 MHz, DMSO) δ 10.05 (s, 1H), 10.02 (s, 1H), 9.90 (s, 1H), 9.81 (s, 1H), 7.94 (t, J=1.8 Hz, 1H), 7.74 (d, J=8.8 Hz, 2H), 7.68 (d, J=8.8 Hz, 2H), 7.48-7.41 (m, 5H), 7.12 (t, J=8.0 Hz, 1H); MS (ESI), 584 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08877970B2 |
| Quelldatensatz | uspto-grants-2014_11 |
| ORD ID | ord-e30dc672821d47d0b44b8dfd786187ae |
| Quellennotiz | uspto-grants-2014_11 |