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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukt3-Methylsulfonylaminophenylboronic acidHCID 2773535—
Edukt7-Bromo-5-methylbenzo[e][1,2,4]triazin-3-amineHCID 24822752—
KatalysatorHCID 178418397HCID 178418397—
ProduktN-[3-(3-amino-5-methyl-benzo[1,2,4]triazin-7-yl)-phenyl]-methanesulfonamideHCID 5983762482%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07456176B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-9a1edb7d233d4b0f909c2c1d1738825f
Quellennotizuspto-grants-2008_11