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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353368Generated: October 30, 2026

1H-Imidazo(4,5-c)pyridine → 1-(2-Trimethylsilylethoxymethyl)-5-azabenzimidazole

https://huagongshe.com/reaction/353368

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Imidazo(4,5-c)pyridineHCID 9227—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
Product1-(2-Trimethylsilylethoxymethyl)-5-azabenzimidazoleHCID 1086868793.6%

Reaction Steps

To a stirred solution of 5-azabenzimidazole (0.300 g, 2.51 mmol) in anhydrous DMF (5 mL) was added N,N-diisopropylethylamine (0.66 mL, 3.80 mmol) followed by 2-(trimethylsilyl)ethoxymethyl chloride (0.54 mL, 3.02 mmol). The resultant solution was heated to 80° C. for 2 h then cooled to room temperature. The reaction mixture was poured into brine (20 mL) and diluted with ethyl acetate (30 mL). The phases were separated and the aqueous phase was extracted with ethyl acetate (3×15 mL). The combined organic extracts were washed with brine (3×5 mL), dried (MgSO4), and concentrated under reduced pressure. Purification of the crude brown oil through a plug of silica gel (CH2Cl2/MeOH, 9:1) provided the 1-(2-trimethylsilylethoxymethyl)-5-azabenzimidazole (0.586 g, 93%) as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06750348B1
Source datasetuspto-grants-2004_06
ORD IDord-1813e1bb46bd46aaaf54a03b04605da4
Source noteuspto-grants-2004_06