HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1170144Erstellt: 25. Oktober 2026
2-Methyl-benzofuran-7-ylamine → 3,5-Difluoro-N-[2-(2-methyl-benzofuran-7-ylamino)-quinolin-5-yl]-benzenesulfonamide
https://huagongshe.com/reaction/1170144
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-Methyl-benzofuran-7-ylamine | HCID 3157485 | — |
| Edukt | N-(2-chloro-quinolin-5-yl)-3,5-difluoro-benzenesulfonamide | HCID 86619497 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 3,5-Difluoro-N-[2-(2-methyl-benzofuran-7-ylamino)-quinolin-5-yl]-benzenesulfonamide | HCID 24988967 | — |
Reaktionsschritte
N-(2-Chloro-quinolin-5-yl)-3,5-difluoro-benzenesulfonamide (150 mg, 0.423 mmol) was dissolved in 3 mL dioxane. Argon was bubbled through the solution for 2 minutes to remove oxygen. (2-Methyl-1-benzofuran-7-yl)amine (245 mg, 1.33 mmol), sodium tert.-butylate (230 mg, 2.40 mmol), 1,1′-bis(diphenylphosphin)ferrocen (36 mg, 0.06 mmol) and 1,1′-bis(diphenylphosphin)ferrocen-palladium(II)chloride (17 mg, 0.02 mmol) were added. The reaction mixture was stirred in a sealed tube at 100° C. for 16 h. The solvent was evaporated and the residue purified by flash chromatography on silica gel (heptane/ethyl acetate 100:0->60:40 gradient). The title compound was obtained as a light brown solid (164 mg, 83%), MS: m/e=466.0 (M+H+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07825253B2 |
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| Quelldatensatz | uspto-grants-2010_11 |
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| ORD ID | ord-123b2c376a72419bbe4f04164744dcf8 |
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| Quellennotiz | uspto-grants-2010_11 |
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