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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711244Generated: October 29, 2026

Potassium Phosphate, Tribasic → (2'-Fluoro-2,4'-bipyridin-5-yl)methanamine

https://huagongshe.com/reaction/711244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Fluoropyridine-4-boronic acidHCID 2783396—
Reactant5-(Aminomethyl)-2-chloropyridineHCID 7020927—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Catalystpalladium(II) acetateHCID 167845—
Solvent(+-)-2-ButanolHCID 6568—
Product(2'-Fluoro-2,4'-bipyridin-5-yl)methanamineHCID 67208618—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a flask containing (6-chloropyridin-3-yl)methanamine 33-2 (642 mg, 4.50 mmol), 2-fluoropyridin-4-ylboronic acid 38-1 (634 mg, 4.50 mmol), Pd(OAc)2 (51 mg, 0.23 mmol), S-Phos (186 mg, 0.45 mmol) and potassium phosphate (2.85 g, 13.50 mmol) under argon was added 2-butanol (5 mL). The mixture was stirred at 100° C. for 10 hours. After cooling to room temperature, the mixture was filtered through celite cake. The filtrate was diluted with ethyl acetate, washed with H2O and brine, dried over Na2SO4, and concentrated to dryness by rotary evaporation. The crude product was purified by silica gel flash chromatography, eluted with 5% methanol containing ˜7N ammonia in dichloromethane to give (2′-fluoro-2,4′-bipyridin-5-yl)methanamine 38-2 as yellow solid. MS m/z 204.1 (M+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181235B2
Source datasetuspto-grants-2015_11
ORD IDord-9d4a00b96b6b4c80a8fe13a980f48807
Source noteuspto-grants-2015_11