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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963878Generated: November 1, 2026

Sodium Carbonate → HCID 66937077, compound

https://huagongshe.com/reaction/1963878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(5-Chloro-2-fluoropyridin-4-yl)boronic acidHCID 44754822—
ReactantHCID 86650610HCID 86650610—
CatalystHCID 178418807HCID 178418807—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 66937077HCID 6693707757.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

5-fluoro-6-(3-fluorobenzylamino)pyridine-2-yl trifluoromethanesulfonate (0.0811 g, 0.220 mmol), 5-chloro-2-fluoropyridin-4-ylboronic acid (0.116 g, 0.661 mmol), and sodium carbonate (0.286 mL, 0.573 mmol, 2M in H2O) were dissolved in DME (2 mL). The solution was then degassed by sparging with argon for 5 min. It was then treated with PdCl2(dppf) CH2Cl2 adduct (0.036 g, 0.044 mmol). The reaction mixture was then heated in the microwave at 120° C. for 10 min. The reaction mixture was then filtered through a pad of Celite. The filtrate was concentrated in vacuo. The resulting residue was subjected to silica gel column chromatography. Elution using 5 EtOAc/95 hexanes to 60 EtOAc/40 hexanes yielded 0.044 g (57%) of 5′-chloro-2′,5-difluoro-N-(3-fluorobenzyl)-2,4′-bipyridin-6-amine. LCMS (m/z): 350.0 (MH+), retention time=1.16 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415381B2
Source datasetuspto-grants-2013_04
ORD IDord-ea65d0876f564d62b9a32158dbbd7950
Source noteuspto-grants-2013_04