HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1029138Erstellt: 26. Oktober 2026
Hydrochloric Acid → 2,3-Dichloro-N-[4-(6-oxo-5,6-dihydro-benzo[c][1,8]naphthyridin-1-yloxy)-phenyl]-benzenesulfonamide
https://huagongshe.com/reaction/1029138
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2,3-Dichlorobenzene-1-sulfonyl chloride | HCID 2734222 | — |
| Edukt | 1-(4-Amino-phenoxy)-5H-benzo[c][1,8]naphthyridin-6-one | HCID 58168367 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 2,3-Dichloro-N-[4-(6-oxo-5,6-dihydro-benzo[c][1,8]naphthyridin-1-yloxy)-phenyl]-benzenesulfonamide | HCID 44205289 | 17,1% |
Reaktionsschritte
Compound 137 (50 mg, 0.16 mmol), 2,3-dichloro-benzenesulfonyl chloride (45 mg, 0.18 mmol), and Et3N (0.07 mL, 0.49 mmol) were suspended in dioxane (2 mL), and stirred overnight at 80° C. The reaction mixture was acidified with 1M HCl, and filtered through an Extrelut column. The column was washed with EtOAc, and the filtrate was concentrated. The crude product was purified via Biotage eluting with a gradient of 25 to 100% EtOAc in hexanes to provide 173 (14 mg, 17% yield) as a white solid. LC-MS (M+H=512, obsd.=512).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08735584B2 |
|---|
| Quelldatensatz | uspto-grants-2014_05 |
|---|
| ORD ID | ord-5a82d64b1cd24b8099be0897252ba853 |
|---|
| Quellennotiz | uspto-grants-2014_05 |
|---|