HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Hydrochloric Acid → 2,4-Dichloro-N-[3,5-dichloro-4-(6-chloro-benzothiazol-2-yloxy)-phenyl]benzenesulfonamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | Benzenesulfonyl chloride, 2,4-dichloro- | HCID 204419 | — |
| Edukt | 3,5-Dichloro-4-(6-chloro-benzothiazol-2-yloxy)-phenylamine | HCID 22148776 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | 2,4-Dichloro-N-[3,5-dichloro-4-(6-chloro-benzothiazol-2-yloxy)-phenyl]benzenesulfonamide | HCID 10209586 | 46,4% |
Reaktionsschritte
A solution of 3,5-dichloro-4-(6-chloro-benzothiazol-2-yloxy) -phenylamine (364) (2.0 g, 5.79 mmol) and 2,4-dichloro benzenesulfonylchloride (1.5 g, 6.08 mmol) in pyridine (10 ml) was stirred at room temperature for 12-hr. Water was added to the reaction mixture, which was then acidified by 2N HCl. Reaction mixture was extracted twice with AcOEt. Organic layer was washed by Brine, dried over MgSO4 and concentrated. Crude residue was purified by column chromatography (H/A=4/1, 80 g of silica gel) to afford title compound (366) (1.49 g, 46%) as a white solid. mp 73-75° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07968567B2 |
| Quelldatensatz | uspto-grants-2011_06 |
| ORD ID | ord-65723c2c1beb415fa873495b991a8f29 |
| Quellennotiz | uspto-grants-2011_06 |