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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259039Generated: October 27, 2026

Potassium Carbonate → 1-[2-(2,6-Dichlorophenylamino)phenyl]-N-[2-(2-hydroxyethoxy)-ethyl]methanesulfonamide

https://huagongshe.com/reaction/1259039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-2,6-dichlorobenzeneHCID 29568—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant1-(2-aminophenyl)-N-[2-(2-hydroxyethoxy)ethyl]methanesulfonamideHCID 62500068—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
Product1-[2-(2,6-Dichlorophenylamino)phenyl]-N-[2-(2-hydroxyethoxy)-ethyl]methanesulfonamideHCID 42640878—

Reaction Conditions

Temperature160 °C

Reaction Steps

To a stirred solution of 1-(2-aminophenyl)-N-[2-(2-hydroxyethoxy)ethyl]-methanesulfonamide (100 mg, 0.37 mmol), 1,3-dichloro-2-bromobenzene (103 mg, 0.46 mmol), K2CO3 (126 mg, 0.99 mmol) and XantPhos (21 mg, 0.04 mmol) in 1,4-dioxane (2 ml) under nitrogen in a microwave tube was added Pd2dba3 (17 mg, 0.019 mmol) in one portion and the tube sealed. The reaction was heated with stirring in a microwave at 160° C. for 30 minutes. The reaction was cooled before filtering through celite. The crude reaction mixture was purified by column chromatography eluting with ethyl acetate:hexane to afford 1-[2-(2,6-Dichlorophenylamino)phenyl]-N-[2-(2-hydroxyethoxy)-ethyl]methanesulfonamide as product (50.5 mg, 33%); Rf (ethyl acetate:hexane 1:1) 0.11; δH (400 MHz, CDCl3) 7.34 (3H, m), 7.23 (1H, t), 7.19 (1H, s), 7.02 (2H, m), 6.60 (1H, d), 5.70 (1H, s), 4.56 (2H, s), 3.70 (2H, s), 3.56 (4H, m), 3.29 (2H, dt) and 2.83 (1H, s); LCMS Rt=3.97 min, m/z (ES+) 441 (M+Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466201B2
Source datasetuspto-grants-2013_06
ORD IDord-5ff088555c104da2a6f1f498eadb9465
Source noteuspto-grants-2013_06