Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659954Generated: November 1, 2026

3-Fluoroaniline → HCID 59409476, compound

https://huagongshe.com/reaction/659954

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-FluoroanilineHCID 9742—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(Dicyclohexylphosphino)biphenylHCID 2734216—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 86643499HCID 86643499—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
ProductHCID 59409476HCID 5940947638.2%

Reaction Conditions

Temperature180 °C

Reaction Steps

In a 5 mL microwave vessel (Biotage) are weighted together 185 mg (0.5 mmole) of 2-(2-Chloro-pyridin-4-yl)-1-(2-fluoro-ethyl)-3-(4-fluoro-phenyl)-1H-pyrrolo[3,2-b]pyridine, 67 mg (0.6 mmoles) of 3-fluorophenyl amine, 2 mg of palladium acetate, 7 mg of biphenylyl dicyclohexylphosphine and 67 mg (0.7 mmole) of sodium t-butoxide in 2.5 mL of toluene. The reaction mixture is then heated at 180° C. for 10 min. under microwave conditions. The reaction mixture is poured into ammonium chloride solution and extracted with ethyl acetate. The organic phase is washed with water and dried over magnesium sulfate. After concentration the solid residue is purified by chromatography on silica gel (ethyl acetate/hexane 1/1) to give 85 mg of {4-[1-(2-Fluoro-ethyl)-3-(4-fluoro-phenyl)-1H-pyrrolo[3,2-b]pyridin-2-yl]-pyridin-2-yl}-(3-fluoro-phenyl)-amine as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084395B2
Source datasetuspto-grants-2011_12
ORD IDord-f3390600c1fc42f08045e461c41a568f
Source noteuspto-grants-2011_12