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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888553Generated: November 4, 2026

Potassium Acetate → 3-[4-(4-Methyl-piperazin-1-yl)-phenyl]-9H-dipyrido[2,3-b;4',3'-d]pyrrole-6-carboxylic acid methyl ester

https://huagongshe.com/reaction/1888553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium AcetateHCID 517044—
Reactant(4-(4-Methylpiperazin-1-yl)phenyl)boronic acidHCID 53316427—
ReactantMethyl 3-bromo-9H-pyrrolo[2,3-b:5,4-c']dipyridine-6-carboxylateHCID 58266719—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Product3-[4-(4-Methyl-piperazin-1-yl)-phenyl]-9H-dipyrido[2,3-b;4',3'-d]pyrrole-6-carboxylic acid methyl esterHCID 58266652—

Reaction Steps

3-Bromo-9H-dipyrido[2,3-b;4′,3′-d]pyrrole-6-carboxylic acid methyl ester (100 mg, 0.327 mmol), 4-(4-methylpiperazin-1-yl)phenylboronic acid, pinacol ester (104 mg, 0.343 mmol) and bis(triphenylphosphine)palladium(II) dichloride (11.5 mg, 0.016 mmol) were suspended in acetonitrile (1.8 mL) and 1N aqueous potassium acetate solution (1.8 mL) and heated under microwave irradiation at 140° C. for 30 minutes. The cooled reaction mixture was diluted with saturated sodium bicarbonate solution and DCM, and the solid removed by filtration. The layers of the resultant filtrate were separated and the aqueous phase was further extracted with DCM. The combined organic phase was dried over sodium sulfate, filtered and concentrated in vacuo. The resultant residue was purified by flash chromatography (silica, 0-20% (MeOH containing 1% triethylamine) in DCM).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501765B2
Source datasetuspto-grants-2013_08
ORD IDord-7bb5bddce87d4317b224d66f8253ba55
Source noteuspto-grants-2013_08