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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659940Generated: October 26, 2026

Sodium Carbonate → 1-Methyl-2-pyridin-4-yl-3-(3-trifluoromethyl-phenyl)-1H-pyrrolo[3,2-b]pyridine

https://huagongshe.com/reaction/659940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-(Trifluoromethyl)phenylboronic acidHCID 2734388—
Reactant3-Iodo-1-methyl-2-pyridin-4-yl-1H-pyrrolo[3,2-b]pyridineHCID 68430585—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product1-Methyl-2-pyridin-4-yl-3-(3-trifluoromethyl-phenyl)-1H-pyrrolo[3,2-b]pyridineHCID 2510059650.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 130 mg (0.39 mmoles) of 3-Iodo-1-methyl-2-pyridin-4-yl-1H-pyrrolo[3,2-b]pyridine in 5 mL of toluene under nitrogen is added a 1 mL of a 2N solution of sodium carbonate, 78 mg (0.4 mmole) of 3-trifluoromethyl phenylboronic acid and 1 mL of ethanol. To the reaction mixture is finally added 24 mg of tetrakistriphenylphosphine palladium before heating at 80° C. for 10 hours. The cooled reaction mixture is then poured into ammonium chloride solution and extracted with ethyl acetate. The organic phase is washed with water and dried over magnesium sulfate. The solid residue after concentration is recrystallized into hexane to afford 70 mg of 1-Methyl-2-pyridin-4-yl-3-(3-trifluoromethyl-phenyl)-1H-pyrrolo[3,2-b]pyridine as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084395B2
Source datasetuspto-grants-2011_12
ORD IDord-bf4a5b477d8646ac92237dfdca00b65e
Source noteuspto-grants-2011_12