HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985106Generated: October 29, 2026
Methyl iodide → 8-Benzyloxy-6-methoxymethyl-2,3-dimethylimidazo[1,2-a]pyridine
https://huagongshe.com/reaction/985106
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 8-Benzyloxy-6-hydroxymethyl-2,3-dimethylimidazo[1,2-a]pyridine | HCID 12106083 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 8-Benzyloxy-6-methoxymethyl-2,3-dimethylimidazo[1,2-a]pyridine | HCID 21873974 | — |
Reaction Steps
A suspension of 1.2 g of 8-benzyloxy-6-hydroxymethyl-2,3-dimethylimidazo[1,2-a]pyridine in 12 ml of dimethylformamide is treated with 0.36 g of 60% strength sodium hydride in paraffin under an inert gas atmosphere, stirred for 30 minutes at room temperature until the evolution of gas is complete, and then treated at room temperature with 0.56 ml of methyl iodide. After a reaction time of one hour, it is poured onto 100 ml of ice water and extracted 3 times with 100 ml of ethyl acetate each time. The organic phases are combined and washed with water. The solvent is stripped off in vacuo and the oily residue is chromatographed on silica gel (eluent: methylene chloride/methanol=100/1). 0.34 g of the title compound of melting point 107° C. (diethyl ether) is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06869949B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-6577fd01df164af1897572f9bdf9c8f6 |
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| Source note | uspto-grants-2005_03 |
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