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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 273527Erstellt: 25. Oktober 2026

Cesium carbonate → 4-[5-methyl-7-(3-nitro-phenyl)-benzo[1,2,4]triazin-3-yl amino]-N-(2-pyrrolidin-1-yl-ethyl)-benzenesulfonamide

https://huagongshe.com/reaction/273527

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
Edukt1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Edukt4-Bromo-N-(2-(pyrrolidin-1-yl)ethyl)benzenesulfonamideHCID 4033090—
Edukt5-Methyl-7-(3-nitro-phenyl)-benzo[1,2,4]triazin-3-ylamineHCID 59837607—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
Produkt4-[5-methyl-7-(3-nitro-phenyl)-benzo[1,2,4]triazin-3-yl amino]-N-(2-pyrrolidin-1-yl-ethyl)-benzenesulfonamideHCID 5983768439%

Reaktionsschritte

In a dry 25 mL round bottom flask, 5-methyl-7-(3-nitro-phenyl)-benzo[1,2,4]triazin-3-ylamine (0.223 g, 0.7935 mmol, 1 equiv), 4-bromo-N-(2-pyrrolidin-1-yl-ethyl)-benzenesulfonamide (0.396 g, 1.19 mmol, 1.5 equiv), cesium carbonate (0.776 g, 2.38 mmol, 3 equiv), 4,5-bis(diphenylphosphino)-9,9-dimethyl xanthene (0.092 g, 0.159 mmol, 0.2 equiv) and tris(dibenzylideneacetone)dipalladium (0.073 g, 0.079 mmol, 0.1 equiv) were combined. The reactants were flushed with argon, diluted with dioxane (10 mL) and outfitted with a reflux condenser. The reaction was heated to reflux for 5 hours, then filtered hot and the solvents were evaporated. Silica gel column purification provided desired product as a yellow powder (0.16 g, 39% yield). MS (ESI+): m/z=582.1

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07456176B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-e298ff2894a24f038612b2965fef1faa
Quellennotizuspto-grants-2008_11