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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481702Generated: October 30, 2026

Imidazole → 6-Bromo-2-((tert-butyldimethylsilyloxy)methyl)imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1481702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant(6-Bromoimidazo[1,2-a]pyridin-2-yl)methanolHCID 15098897—
SolventDichloromethaneHCID 6344—
Product6-Bromo-2-((tert-butyldimethylsilyloxy)methyl)imidazo[1,2-a]pyridineHCID 7128478969%

Reaction Steps

To solution of (6-bromoimidazo[1,2-a]pyridin-2-yl)methanol (3.21 g, 14.13 mmol) in DCM (50 mL) was added imidazole (1.30 g, 19.09 mmol) followed by TBSCl (2.60 g, 17.25 mmol). Reaction mixture was stirred at room temperature for 30 min then was diluted with DCM (50 mL) and washed with H2O (50 mL). Organic phase was washed with NaCl (aqueous saturated, 50 mL) and dried over Na2SO4. Solvent was concentrated and residue purified by column chromatography using EtOAc/hexanes (gradient 0-50%) to afford 6-bromo-2-((tert-butyldimethylsilyloxy)methyl)imidazo[1,2-a]pyridine (3.32 g) in 69% yield as pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409905B2
Source datasetuspto-grants-2016_08
ORD IDord-0aee9ea0144641f7addfc5121ad05b2a
Source noteuspto-grants-2016_08