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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891236Generated: November 1, 2026

Ethanol → [3-(6-Aminopyridin-3-yl)phenyl]methanol

https://huagongshe.com/reaction/1891236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant2-Amino-5-bromopyridineHCID 70622—
Reactant[3-(Hydroxymethyl)phenyl]boronic acidHCID 2734662—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product[3-(6-Aminopyridin-3-yl)phenyl]methanolHCID 4423237786.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

2.0 g of tetrakis(triphenylphosphine)palladium and 75 ml of a 2M solution of sodium carbonate are added to a round-bottomed flask containing a solution of 5.0 g of 5-bromopyridin-2-ylamine in 140 ml of toluene, 5.7 g of 3-(hydroxymethyl)phenylboronic acid and 70 ml of ethanol degassed beforehand. The mixture is heated at 80° C. for 16 h. After cooling, the reaction mixture is concentrated under reduced pressure. The residue is taken up between water and ethyl acetate. The organic phase is separated, dried and concentrated under reduced pressure. The residue is purified by silica gel chromatography, elution being carried out with a dichloromethane/methanol mixture. 4.99 g of compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507520B2
Source datasetuspto-grants-2013_08
ORD IDord-e1cd0982595a41b5a19da61b6a9c4575
Source noteuspto-grants-2013_08