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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376681Generated: November 1, 2026

Potassium Carbonate → HCID 178464507, compound

https://huagongshe.com/reaction/2376681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantLithium ChlorideHCID 433294—
ReactantPotassium AcetateHCID 517044—
ReactantBis(pinacolato)diboraneHCID 2733548—
Reactant2-bromo-N,N-diethylbenzenesulfonamideHCID 26370029—
ReactantHCID 178493175HCID 178493175—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178464507HCID 17846450734.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 0.438 g of N,N-diethylbromobenzenesulfonamide, 0.42 g of bis-(pinacolato)diboron, 0.025 g of 1,1′-bis-(diphenylphosphino)-ferrocene, 0.033 g of [1,1′-bis(diphenyl-phosphino)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 N2 for 7 hours. To the resulting mixture 10 ml of degassed dioxane, 0.371 g of 2-[2-(4-methoxypyridin-2-yl)ethyl]-6-iodo-3H-imidazo[4,5-b]pyridine (starting material A1), 0.113 g of tetrakis(triphenylphos-phine)-palladium(0) and a solution of 0.27 g of potassium carbonate and 0.083 g of lithium chloride in 10 ml of degassed water are added under N2. The mixture is heated to reflux under N2 for 16 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 30-25:1). Concentration of the chromatographically pure fractions and crystallisation from ethylacetate gives 0.155 g of the title compound as a solid of m.p. 127-129° C. The mass spectrum shows the molecular peak MH+ at 466.3 Da.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468377B2
Source datasetuspto-grants-2008_12
ORD IDord-f2329cd56de04e5c918445fc29dd3818
Source noteuspto-grants-2008_12