Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179418Generated: October 31, 2026

Potassium Carbonate → HCID 178493159, compound

https://huagongshe.com/reaction/1179418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-N-(4-methylphenyl)benzene-1-sulfonamideHCID 221872—
ReactantLithium ChlorideHCID 433294—
ReactantPotassium AcetateHCID 517044—
ReactantHCID 178493175HCID 178493175—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178493159HCID 17849315945.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 0.489 g of N-p-tolyl-4-bromobenzenesulfonamide, 0.42 g of bis-(pinacolato)-diboron, 0.025 g of 1,1′-bis-(diphenylphosphino)-ferrocene, 0.033 g of [1,1′-is(diphenylphosphino)-ferrocene]palladium-dichloride (complex with CH2Cl2), 0.442 g of potassium acetate in 6 ml of degassed dioxane are heated to 90° C. in a sealed tube under N2for 17 hours. To the resulting mixture 5 ml of degassed dioxane, 0.371 g of 2-[2-(4methoxypyridin-2-yl)ethyl]-6-iodo-3H-imidazo[4,5-b]pyridine (starting material A1), 0.113 g of tetrakis(triphenylphosphine)-palladium(0) and a solution of 0.27 g of potassium carbonate and 0.083 g of lithium chloride in 5 ml of degassed water are added under N2. The tube is sealed again, the mixture is heated to 120° under N2 for 6.5 hours and, after cooling, addition of water and adjusting the pH to 7, it is extracted three times with dichloromethane. The combined organic phases are dried over sodium sulfate, concentrated and the residue is chromatographed on a silica gel column (dichloromethane/methanol 25-15:1). Concentration of the chromatographically pure fractions and crystallisation from ethylacetate/acetonitril (1:1) gives 0.22 g of the title compound as a solid of m.p. 219-220° C. The mass spectrum shows the molecular peak MH+ at 500.3 Da.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279488B2
Source datasetuspto-grants-2007_10
ORD IDord-c308e40a43a543238f33815b45a126dc
Source noteuspto-grants-2007_10