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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273499Generated: October 27, 2026

Cesium carbonate → HCID 59837591, compound

https://huagongshe.com/reaction/273499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant3-bromo-N-(2-(dimethylamino)ethyl)benzenesulfonamideHCID 3861789—
Reactant7-(2-Chloro-5-methoxyphenyl)-5-methylbenzo[e][1,2,4]triazin-3-amineHCID 24822753—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59837591HCID 59837591—

Reaction Conditions

Temperature100 °C

Reaction Steps

7-(2-chloro-5-methoxy-phenyl)-5-methyl-benzo[1,2,4]triazin-3-ylamine (0.333 mmol, 1.0 equiv), 3-bromo-N-(2-dimethylamino-ethyl)-benzenesulfonamide (0.499 mmol, 1.5 equiv), Cs2CO3 (0.999 mmol, 3.0 equiv), Pd2(dba)3 (0.0333 mmol, 0.1 equiv), and Xantphos (0.0666 mmol, 0.2 equiv) were dissolved in 7 mL dioxane. The reaction was placed under an argon atmosphere and refluxed at 100° C. for 18 h. The organics were filtered to remove excess inorganics, dissolved in EtOAc, washed with saturated NaHCO3 and brine, dried over Na2SO4 and concentrated under reduced pressure to give 3-[7-(2-chloro-5-methoxy-phenyl)-5-methyl-benzo[1,2,4]triazin-3-ylamino]-N-(2-dimethylamino-ethyl)-benzenesulfonamide, which was precipitated using EtOAc/hexanes (1:5 v/v) to give a dark orange solid (168.4 mg, 96% yield). Rf=0.50 MS (ES+) m/z=527.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456176B2
Source datasetuspto-grants-2008_11
ORD IDord-077af60ea1f4444cad3493ecebaa34db
Source noteuspto-grants-2008_11