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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233499Generated: October 31, 2026

Potassium Carbonate → HCID 178493150, compound

https://huagongshe.com/reaction/2233499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantLithium ChlorideHCID 433294—
ReactantPotassium AcetateHCID 517044—
ReactantHCID 3680172HCID 3680172—
ReactantHCID 178493175HCID 178493175—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178493150HCID 17849315084.9%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 0.406 g of 1-(4-bromo-benzene-sulfonyl)-4-(4-cyanophenyl)-piperazine, 0.28 g of bis-(pinacolato)-diboron, 0.017 g of 1,1′-bis-(diphenylphosphino)-ferrocene, 0.022 g of [1,1′-bis(diphenyl-phosphino)ferrocene]palladium-dichloride (complex with CH2Cl2), 0.294 g of potassium acetate in 6 ml of degassed dioxane are heated to 85° C. in a sealed tube under N2 for 18 hours. To the resulting mixture 4 ml of degassed dioxane, 0.228 g of 2-[2-(4-methoxypyridin-2-yl)ethyl]-6-iodo-3H-imidazo[4,5-b]pyridine (starting material A1), 0.069 g of tetrakis(triphenylphosphine)-palladium(0) and a solution of 0.165 g of potassium carbonate and 0.051 g of lithium chloride in 4 ml of degassed water are added under N2. The tube is sealed again, the mixture is heated to 110° under N2 for 5 hours and, after cooling, addition of water and adjusting the pH to 7, it is extracted three times with ethylacetate. The combined organic phases are dried over sodium sulfate, concentrated and the residue is crystallized from ethylacetate. Recrystallization from ethylacetate and then from acetonitril gives 0.295 g of the title compound as a brownish solid of m.p. 217-219° C. The mass spectrum shows the molecular peak MH+ at 580.5 Da.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709488B2
Source datasetuspto-grants-2010_05
ORD IDord-caf2a5ffd4c04b7b8c3779d60ae276fb
Source noteuspto-grants-2010_05