HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 273525Erstellt: 26. Oktober 2026
Sodium Carbonate → N-[3-(3-amino-5-methyl-benzo[1,2,4]triazin-7-yl)-phenyl]-methanesulfonamide
https://huagongshe.com/reaction/273525
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 3-Methylsulfonylaminophenylboronic acid | HCID 2773535 | — |
| Edukt | 7-Bromo-5-methylbenzo[e][1,2,4]triazin-3-amine | HCID 24822752 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Produkt | N-[3-(3-amino-5-methyl-benzo[1,2,4]triazin-7-yl)-phenyl]-methanesulfonamide | HCID 59837624 | 82% |
Reaktionsschritte
An oven dried 25 mL round bottom flask was charged with 7-bromo-5-methyl-benzo[1,2,4]triazin-3-ylamine (0.889 g, 3.72 mmol, 1 equiv), 3-(methylsulfonylamino) phenyl boronic acid (1.12 g, 5.21 mmol, 1.4 equiv), sodium carbonate (1.57 g, 14.9 mmol, 4 equiv) and tetrakis(triphenylphosphine)palladium(0) (0.43 g, 0.372 mmol, 0.1 equiv). The reactants were flushed with argon and diluted with ethylene glycol dimethyl ether (20 mL), ethanol (5 mL) and DI water (5 mL). The reaction vessel was outfitted with condenser and refluxed for 4 hours. The reaction was filtered hot and diluted with ethyl acetate. The Organic layer was isolated and concentrated to a dark residue. This was dissolved in DMF (6 mL) and slowly diluted with water so as to precipitate out the product. Solids were filtered off and dried to yield an orange solid (1 g, 82% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07456176B2 |
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| Quelldatensatz | uspto-grants-2008_11 |
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| ORD ID | ord-9a1edb7d233d4b0f909c2c1d1738825f |
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| Quellennotiz | uspto-grants-2008_11 |
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