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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762208Generated: October 26, 2026

2-Amino-3-methoxymethoxypyridine → HCID 14368347, compound

https://huagongshe.com/reaction/1762208

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-3-methoxymethoxypyridineHCID 14368345—
Reactant3-Mesyloxy-5-hexyn-2-oneHCID 14368346—
SolventEthanolHCID 702—
ProductHCID 14368347HCID 1436834721.3%

Reaction Steps

A solution of 2-amino-3-methoxymethoxypyridine (7.5 g) and 3-mesyloxy-5-hexyn-2-one (10.18 g) in ethanol (150 ml) was refluxed for 46.5 hours and then evaporated in vacuo. To the residue was added 20% sulfuric acid (75 ml) and the mixture was stirred for 5 hours at room temperature. The mixture was made alkaline with sodium bicarbonate and extracted with chloroform. The extract was washed with brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was purified by column chromatography on silica gel (30 g) with chloroform and then a mixture of chloroform and methanol (30:1 to 20:1) as eluents. The eluates were evaporated in vacuo and the residue was recrystallized from a mixture of ethyl acetate and n-hexane to give 8-hydroxy-2-methyl-3-(2-propynyl)imidazo[1,2-a]pyridine (1.93 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04831041
Source datasetuspto-grants-1989_05
ORD IDord-98c2829e74c34458be64628010fd79be
Source noteuspto-grants-1989_05