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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367675Generated: November 2, 2026

Water → 5-(3-Fluorophenyl)pyridin-3-amine

https://huagongshe.com/reaction/2367675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant3-Amino-5-bromopyridineHCID 817681—
Reactant3-Fluorophenylboronic acidHCID 2733986—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product5-(3-Fluorophenyl)pyridin-3-amineHCID 4631188783.1%

Reaction Conditions

Temperature180 °C

Reaction Steps

To a microwave vial was added 3-amino-5-bromopyridine (LII) (0.400 g, 2.31 mmol), 3-fluorophenyl boronic acid (XLIX) (0.356 g, 2.54 mmol), tetrakis(triphenylphosphine)palladium(0) (0.133 g, 0.116 mmol), potassium phosphate (0.736 g, 3.47 mmol), water (1 mL), and DMF (5 mL). The reaction vial was capped, purged with argon and heated under microwave irradiation for 1 h at 180° C. The solution was filtered through a pad of Celite and concentrated under vacuum. The residue was purified by column chromatography (4:6 EtOAc:hexanes→7:3 EtOAc:hexanes) to afford the 5-(3-fluorophenyl)pyridin-3-amine (LIII) (0.360 g, 1.92 mmol, 83% yield) as a yellow-white solid. ESIMS found for C11H9FN2 m/z 189.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697887B2
Source datasetuspto-grants-2014_04
ORD IDord-85db9d0917fb4ec0bfa7e6b11ca9468a
Source noteuspto-grants-2014_04