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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583705Generated: October 31, 2026

4-Methoxybenzylamine → 2-[2-(4-Methoxybenzylamino)pyridin-6-yl]ethanol

https://huagongshe.com/reaction/583705

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzylamineHCID 75452—
Reactant2-(6-Chloropyridin-2-yl)ethanolHCID 18928556—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product2-[2-(4-Methoxybenzylamino)pyridin-6-yl]ethanolHCID 18518348—

Reaction Steps

Chloropyridine 30-2 (150 mg, 0.95 mmol) and 4-methoxybenzylamine (4 mL, 31 mmol) were combined neat and heated in a sealed tube at 160° for 4 days. After diluting with EtOAc and water the pH was adjusted to 7 phases separated and the organic phase was washed with brine, dried (MgSO4) and concentrated. Flash chromatography (twice on silica, 50% and 40% EtOAc/hexane) provided 30-3 as a yellow semi-solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05929120
Source datasetuspto-grants-1999_07
ORD IDord-1ce2e5ed8da04346b5eb2c55632577bc
Source noteuspto-grants-1999_07