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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963869Generated: October 26, 2026

1,2-Dimethoxyethane → 5'-Chloro-2'-fluoro-6-(3-fluorobenzyloxy)-2,4'-bipyridine

https://huagongshe.com/reaction/1963869

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium CarbonateHCID 10340—
Reactant(5-Chloro-2-fluoropyridin-4-yl)boronic acidHCID 44754822—
Reactant2-Bromo-6-(3-fluorobenzyloxy)pyridineHCID 86650608—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
Product5'-Chloro-2'-fluoro-6-(3-fluorobenzyloxy)-2,4'-bipyridineHCID 6693690358.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-bromo-6-(3-fluorobenzyloxy)pyridine (145 mg, 0.514 mmol), 5-chloro-2-fluoropyridin-4-ylboronic acid (144 mg, 0.822 mmol), PalladiumTetrakis (71.3 mg, 0.062 mmol), DME (3 ml), and 12M sodium carbonate (1.028 ml, 2.056 mmol) was reaction mixture was stirred at 100° C. for 3 hr, followed by LCMS. The reaction mixture was cooled, diluted with 10 ml of ethyl acetate, filtered and concentrated to yield a crude product, which was purified by silica gel chromatography using a 12 g column eluting from 0%-20% ethyl acetate with hexane. The desired fractions were concentrated to constant mass, giving 100 mg of titled compound as a free base. LCMS (m/z): 333.1 (MH+), retention time=1.26 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415381B2
Source datasetuspto-grants-2013_04
ORD IDord-d5698488a57246b6ba5c7c7a28c04498
Source noteuspto-grants-2013_04