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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711239Generated: October 28, 2026

Potassium Phosphate, Tribasic → (2'-Fluoro-3-methyl-2,4'-bipyridin-5-yl)methanamine

https://huagongshe.com/reaction/711239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Fluoropyridine-4-boronic acidHCID 2783396—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Reactant(6-Chloro-5-methylpyridin-3-yl)methanamine hydrochlorideHCID 53395592—
Catalystpalladium(II) acetateHCID 167845—
Product(2'-Fluoro-3-methyl-2,4'-bipyridin-5-yl)methanamineHCID 67208684—

Reaction Steps

To a reaction vial was added (6-chloro-5-methylpyridin-3-yl)methanamine HCl salt 30-4 (738 mg, 3.8 mmol), 2-fluoropyridin-4-ylboronic acid 30-5 (800 mg, 5.7 mmol), Pd(OAc)2 (106 mg, 0.47 mmol), S-Phos (194 mg, 0.47 mmol) and K3PO4 (2.0 g, 9.5 mmol). The vial was evacuated and backfilled with nitrogen, and 2-butanol (5 mL) was added via syringe. The reaction was stirred at room temperature for 10 mins and then 100° C. for 3 hours. After cooling to room temperature, the reaction mixture was partitioned between DCM and H2O, and extracted with DCM three times. The organic phase was combined and dried. The crude product was purified by silica gel flash chromatography, eluted with 10% methanol in DCM to give (2′-fluoro-3-methyl-2,4′-bipyridin-5-yl)methanamine 30-5. MS m/z 218.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181235B2
Source datasetuspto-grants-2015_11
ORD IDord-3518541786da4c3b9ec46e1b2a1d89fd
Source noteuspto-grants-2015_11