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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711254Generated: October 26, 2026

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

https://huagongshe.com/reaction/711254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Reactant2-(Trifluoromethyl)pyridine-4-boronic acidHCID 45158880—
Reactant(6-Chloro-5-methylpyridin-3-yl)methanamine hydrochlorideHCID 53395592—
Catalystpalladium(II) acetateHCID 167845—
Solvent(+-)-2-ButanolHCID 6568—
Product(2'-(Trifluoromethyl)-2,4'-bipyridin-5-yl)methanamineHCID 67208623—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a flask containing (6-chloro-5-methylpyridin-3-yl)methanamine 30-4 (500 mg, 2.20 mmol), 2-(trifluoromethyl)pyridin-4-ylboronic acid 33-1 (418 mg, 2.20 mmol), Pd(OAc)2 (29 mg, 0.11 mmol), S-Phos (91 mg, 0.22 mmol) and potassium phosphate (1.40 g, 6.60 mmol) under Argon was added 2-butanol (4 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, and eluted with 5% methanol containing ˜7N ammonia in dichloromethane to give (2′-(trifluoromethyl)-2,4′-bipyridin-5-yl)methanamine 48-1 as a dark yellow solid. MS m/z 268.1 (M+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181235B2
Source datasetuspto-grants-2015_11
ORD IDord-5f65d11c70b841fc8e89cd250e4370ec
Source noteuspto-grants-2015_11