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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725464Generated: November 1, 2026

Imidazole → 6-({[Tert-butyl(dimethyl)silyl]oxy}methyl)pyridin-2-amine

https://huagongshe.com/reaction/1725464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant6-Amino-2-pyridinemethanolHCID 11182606—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product6-({[Tert-butyl(dimethyl)silyl]oxy}methyl)pyridin-2-amineHCID 2113223078.1%

Reaction Steps

1.26 g (10.2 mmol) of 2-amino-6-hydroxymethylpyridine (Journal of Heterocyclic Chemistry, 2001, 38, 173) was dissolved in 5.1 mL of dimethylformamide and 1.7 g (25 mmol) of imidazole was added thereto. Under cooling with ice, 1.8 g (12 mmol) of tert-butyldimethylsilyl chloride was added thereto followed by stirring at room temperature for 1 hour. The reaction solution was diluted with ethyl acetate and the organic layer was washed with water and brine. This was dried over magnesium sulfate and filtered, and the filtrate was concentrated. The resulting residue was purified by a silica gel column chromatography to give 1.9 g of the title compound as an orange-colored oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491720B2
Source datasetuspto-grants-2009_02
ORD IDord-f0f6f5d84a224f36a2912da0acad7718
Source noteuspto-grants-2009_02