HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5470Generated: October 25, 2026
Water → 5-[2-(N-benzylmethylsulfonylamino)ethyloxy]imidazo[1,2-a]pyridine
https://huagongshe.com/reaction/5470
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Chloroimidazo[1,2-A]pyridine | HCID 10953722 | — |
| Reactant | 2-(N-benzylmethylsulfonylamino)-1-ethanol | HCID 14947395 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-[2-(N-benzylmethylsulfonylamino)ethyloxy]imidazo[1,2-a]pyridine | HCID 23362951 | 39.4% |
Reaction Steps
To a suspension of 60% sodium hydride in oil (0.20 g, 5 mmoles) in dimethylformamide (20 ml) was added 2-(N-benzylmethylsulfonylamino)-1-ethanol (1.14 g, 5 mmoles) with stirring under ice-cooling and the mixture was stirred at room temperature for 30 minutes. To this reaction mixture was added 5-chloroimidazo[1,2-a]pyridine (0.763 g, 5 mmoles) with stirring under ice-cooling, followed by stirring at 80° C. for 16 hours. After cooling, water was added to the reaction mixture, which was extracted with ethyl acetate and dried. After the solvent was distilled off, the residue was purified by column chromatography [eluent: ethyl acetate/hexane (1:1)→ethyl acetate/hexane (2:1)] to obtain 0.68 g of the desired product (39.4%, pale yellow oily product).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05244908 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-e3132aba721d4308b7846406e0b07587 |
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| Source note | uspto-grants-1993_09 |
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