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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870005Generated: October 31, 2026

(6-Methoxypyridin-3-yl)boronic acid → HCID 68722356, compound

https://huagongshe.com/reaction/870005

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6-Methoxypyridin-3-yl)boronic acidHCID 2734368—
ReactantHCID 89228782HCID 89228782—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
SolventSodium CarbonateHCID 10340—
ProductHCID 68722356HCID 6872235633.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of N-(6-chloro-4-methylpyridin-2-yl)-1-(2,3-dihydrobenzofuran-6-yl)cyclopropanecarboxamide (50.0 mg, 0.15 mmol), 2-methoxypyridine-5-boronic acid (23.0 mg, 0.15 mmol), and tetrakis(triphenylphosphine)palladium (0) (8.8 mg, 0.0076 mmol) in 1,2-dimethoxyethane (1.0 mL) and 2 M Na2CO3 (0.2 mL) was stirred at 80° C. for 16 hours under N2 atmosphere. The reaction mixture was diluted with ethyl acetate (5 mL), dried over Na2SO4, filtered and evaporated under reduced pressure. The crude product was purified by column chromatography on silica gel (0-30% ethyl acetate in hexane) to yield 20 mg (32%) of 1-(2,3-dihydrobenzofuran-6-yl)-N-(6′-methoxy-4-methyl-2,3′-bipyridin-6-yl)cyclopropanecarboxamide. ESI-MS m/z calc. 401.2. found 402.0 (M+1)+. Retention time 1.94 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969386B2
Source datasetuspto-grants-2015_03
ORD IDord-a076763f5d994c399617adc925a409d9
Source noteuspto-grants-2015_03