Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869929Generated: October 30, 2026

(6-Methoxypyridin-3-yl)boronic acid → HCID 68739156, compound

https://huagongshe.com/reaction/869929

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6-Methoxypyridin-3-yl)boronic acidHCID 2734368—
ReactantHCID 87556410HCID 87556410—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
SolventSodium CarbonateHCID 10340—
ProductHCID 68739156HCID 6873915693.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

To N-(6-chloro-5-methylpyridin-2-yl)-1-(2,3-dihydro-1H-inden-5-yl)cyclopropanecarboxamide (0.132 g, 0.4030 mmol), 6-methoxypyridin-3-ylboronic acid (0.092 g, 0.6045 mmol) and tetrakis(triphenylphosphine)palladium (0) (0.046 g, 0.04030 mmol) in 1,2-dimethoxyethane (4.4 mL), 2 M Na2CO3 (600 μL) was added. The reaction mixture was stirred and heated at 80° C. for 22 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 1-(2,3-dihydro-1H-inden-5-yl)-N-(6′-methoxy-3-methyl-2,3′-bipyridin-6-yl)cyclopropanecarboxamide as a white solid (0.150 g, 93.17%). ESI-MS m/z calc. 399.48, found 400.5 (M+1)+. Retention time 2.17 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969386B2
Source datasetuspto-grants-2015_03
ORD IDord-9fd520d413294ca284973f59c849bb36
Source noteuspto-grants-2015_03