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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63598Generated: October 30, 2026

Potassium Carbonate → HCID 118468018, compound

https://huagongshe.com/reaction/63598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Methoxyphenylboronic acidHCID 2733958—
ReactantHCID 70952154HCID 70952154—
CatalystHCID 178418397HCID 178418397—
SolventToluene ethanolHCID 21863594—
ProductHCID 118468018HCID 11846801898%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of 3-phenyl-5-bromo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine (309 mg, 0.75 mmol) in a 3:1 toluene/ethanol mixture (24 ml) are added 2-methoxy-benzene boronic acid (125 mg, 0.83 mmol), K2CO3 (2.4 ml of 2 M solution in water, 4.5 mmol), Pd(PPh3)4 (1.5 mol %), and the mixture is heated at 85° C. for 2 hours under argon. The mixture is cooled to room temperature, concentrated under a vacuum and redissolved in a water/CH2Cl2 mixture. The aqueous phase is extracted several times with CH2Cl2 and the combined organic phases are dried on MgSO4. The solvent is evaporated under reduced pressure and the residue purified by flash chromatography on silica gel (100% CH2Cl2) to yield the purified product in the form of a colorless oil with a yield of 98%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447093B2
Source datasetuspto-grants-2016_09
ORD IDord-dd169ea86f934a97b25c6ab5bfbae715
Source noteuspto-grants-2016_09