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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196452Generated: October 26, 2026

Imidazole → 5-[3-(tert-Butyldimethylsilanyloxymethyl)phenyl]pyridin-2-ylamine

https://huagongshe.com/reaction/2196452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant[3-(6-Aminopyridin-3-yl)phenyl]methanolHCID 44232377—
ReactantTert-butyldimethylsilane chlorideHCID 131722836—
SolventTetrahydrofuranHCID 8028—
Product5-[3-(tert-Butyldimethylsilanyloxymethyl)phenyl]pyridin-2-ylamineHCID 4423237889.3%

Reaction Steps

4.99 g of [3-(6-aminopyridin-3-yl)phenyl]methanol are placed in a round-bottomed flask and dissolved in 240 ml of tetrahydrofuran. 2.2 g of 1H-imidazole are added thereto, followed by 4.51 g of tert-butyldimethylsilane chloride, and the mixture is left to stir at ambient temperature for 48 hours. The reaction mixture is then hydrolysed with water, and the organic phase, which has been extracted with ethyl acetate, is separated, dried over magnesium sulphate and concentrated under reduced pressure. The residue obtained is purified by silica gel chromatography, elution being carried out with a heptane/ethyl acetate mixture. 7.0 g of compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338451B2
Source datasetuspto-grants-2012_12
ORD IDord-f9556880a3d8426c89bfce34dc9eb02a
Source noteuspto-grants-2012_12