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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1H-Imidazo(4,5-c)pyridine | HCID 9227 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Chloromethyl 2-(trimethylsilyl)ethyl ether | HCID 2724271 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 1-(2-Trimethylsilylethoxymethyl)-5-azabenzimidazole | HCID 10868687 | 93.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06750348B1 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-1813e1bb46bd46aaaf54a03b04605da4 |
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| Source note | uspto-grants-2004_06 |
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