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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550891Generated: October 25, 2026

Methane → ethyl 3-(4-aminophenyl)-1H-pyrrolo[2,3-c]pyridine-2-carboxylate

https://huagongshe.com/reaction/550891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantPotassium FluorideHCID 522689—
Reactant(4-Aminophenyl)boronic acid hydrochlorideHCID 2734614—
Reactantethyl 3-bromo-1H-pyrrolo[2,3-c]pyridine-2-carboxylateHCID 57445353—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
Solvent1,4-DioxaneHCID 31275—
Productethyl 3-(4-aminophenyl)-1H-pyrrolo[2,3-c]pyridine-2-carboxylateHCID 5744535257.4%

Reaction Steps

To a solution of 1 g of ethyl 3-bromo-1H-pyrrolo[2,3-c]pyridine-2-carboxylate in 100 mL of dioxane are added 773 mg of 4-aminophenylboronic acid hydrochloride and 1.1 g of potassium fluoride in 9 mL of water. The reaction mixture is stirred under an argon atmosphere for 15 minutes. 425 mg of tetrakis(triphenylphosphine)palladium(0) and 630 μL of triethylamine are added. The reaction mixture is stirred for 17 hours at reflux. After treating with carbon black and then filtering through Celite®, the filtrate is concentrated under reduced pressure. The residue is purified by flash chromatography on a column of silica (60; 35-70 μM), eluting with a mixture of dichloromethane, methanol and acetonitrile (90/5/5 by volume). 600 mg of ethyl 3-(4-aminophenyl)-1H-pyrrolo[2,3-c]pyridine-2-carboxylate are obtained, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947706B2
Source datasetuspto-grants-2011_05
ORD IDord-cb85bc5963f54265acc359ec33f26a0a
Source noteuspto-grants-2011_05