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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179405Generated: October 31, 2026

Potassium Carbonate → HCID 178493151, compound

https://huagongshe.com/reaction/1179405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantLithium ChlorideHCID 433294—
ReactantPotassium AcetateHCID 517044—
ReactantHCID 68411193HCID 68411193—
ReactantHCID 178493175HCID 178493175—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178493151HCID 1784931518.4%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 0.675 g of 1-(4-bromo-benzene-sulfonyl)-4-(3,5-dichlorphenyl)-piperazine, 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 8 ml of degassed dioxane are heated to 85° C. in a sealed tube under N2 for 6 hours. To the resulting mixture 4 ml of degassed dioxane, 0.342 g of 2-[2-(4-methoxypyridin-2-yl)ethyl]-6-iodo-3H-imidazo[4,5b]pyridine (starting material A1), 0.104 g of tetrakis(triphenylphosphine)-palladium(0) and a solution of 0.25 g of potassium carbonate and 0.076 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 17 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 chromatographed on a silica gel column (dichloromethane/methanol 28-24:1). Concentration of the chromatographically pure fractions and crystallization of the residue from ethylacetate gives 0.047 g of the title compound as a solid of m.p. 220-222° C. The mass spectrum shows the molecular peak MH+ at 623.5 Da.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279488B2
Source datasetuspto-grants-2007_10
ORD IDord-bb0db9fbf19344cf9dc984b84b5e5320
Source noteuspto-grants-2007_10