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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471683Generated: October 30, 2026

Potassium Carbonate → 5-[(Imidazo[1,2-A]pyridin-8-Yl)methoxy]-2-Methoxypyridine-4-Carbaldehyde

https://huagongshe.com/reaction/1471683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant8-(Chloromethyl)imidazo[1,2-a]pyridineHCID 21661582—
Reactant5-Hydroxy-2-methoxyisonicotinaldehydeHCID 72212498—
SolventDimethylformamideHCID 6228—
Product5-[(Imidazo[1,2-A]pyridin-8-Yl)methoxy]-2-Methoxypyridine-4-CarbaldehydeHCID 7162081138%

Reaction Conditions

Temperature125 °C

Reaction Steps

A mixture of 5-hydroxy-2-methoxyisonicotinaldehyde (723.6 mg, 4.7 mmol), 8-(chloromethyl)-imidazol[1,2-a]pyridine (785 mg, 4.7 mmol), and K2CO3 (1.9 g, 14.1 mmol) in DMF (20 mL) was heated at microwave reactor at 125° C. for 15 min. The mixture was filtered and concentrated. The residue was purified on silica gel (50-100% EtOAc in hexanes) to give 5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-methoxyisonicotinaldehyde (500 mg, 38%) as an off-white solid. 1H NMR (400 MHz; DMSO) δ=10.37 (s, 1H), 8.58 (d, 1H), 8.39 (s, 1H), 8.02 (s, 1H), 7.61 (s, 1H), 7.44 (d, 1H), 6.98 (s, 1H), 6.93 (t, 1H), 5.61 (s, 2H), 3.84 (s, 3H). LRMS (M+H+) m/z 284.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012450B2
Source datasetuspto-grants-2015_04
ORD IDord-b99d7cf281554e0bb8e207f23bd5fa6f
Source noteuspto-grants-2015_04