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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870003Generated: October 30, 2026

(6-Methoxypyridin-3-yl)boronic acid → HCID 68723757, compound

https://huagongshe.com/reaction/870003

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6-Methoxypyridin-3-yl)boronic acidHCID 2734368—
ReactantHCID 89228827HCID 89228827—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
SolventSodium CarbonateHCID 10340—
ProductHCID 68723757HCID 6872375749.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of N-(6-chloro-5-methylpyridin-2-yl)-1-(2,3-dihydrobenzofuran-6-yl)cyclopropanecarboxamide (50.0 mg, 0.15 mmol), 2-methoxypyridine-5-boronic acid (23.26 mg, 0.15 mmol), and tetrakis(triphenylphosphine)palladium (0) (9.0 mg, 0.0076 mmol) in 1,2-dimethoxyethane (1.5 mL) and 2 M Na2CO3 (0.3 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 30 mg (49%) of 1-(2,3-dihydrobenzofuran-6-yl)-N-(2′-methoxy-3-methyl-2,4′-bipyridin-6-yl)cyclopropanecarboxamide. ESI-MS m/z calc. 401.2. found 402.0 (M+1)+. Retention time 1.83 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969386B2
Source datasetuspto-grants-2015_03
ORD IDord-b357e37e73654f09a29a6c2b5bcc3ee8
Source noteuspto-grants-2015_03