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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273527Generated: October 26, 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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant4-Bromo-N-(2-(pyrrolidin-1-yl)ethyl)benzenesulfonamideHCID 4033090—
Reactant5-Methyl-7-(3-nitro-phenyl)-benzo[1,2,4]triazin-3-ylamineHCID 59837607—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Product4-[5-methyl-7-(3-nitro-phenyl)-benzo[1,2,4]triazin-3-yl amino]-N-(2-pyrrolidin-1-yl-ethyl)-benzenesulfonamideHCID 5983768439%

Reaction Steps

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456176B2
Source datasetuspto-grants-2008_11
ORD IDord-e298ff2894a24f038612b2965fef1faa
Source noteuspto-grants-2008_11