HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121484Generated: November 2, 2026
Methyl iodide → 8-Benzyloxy-6-methoxymethyl-2,3-dimethylimidazo[1,2-a]pyridine
https://huagongshe.com/reaction/2121484
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
Under an atmosphere of inert gas, a suspension of 1.2 g of 8-benzyloxy-6-hydroxymethyl-2,3-dimethylimidazo[1,2-a]pyridine in 12 ml of dimethylformamide is admixed with 0.36 g of 60% sodium hydride in paraffin, and the mixture is stirred at room temperature for 30 minutes, until the generation of gas has ceased, and then, at room temperature, admixed with 0.56 ml of methyl iodide. After a reaction time of one hour, the mixture is poured into 100 ml of ice-water and extracted three times with in each case 100 ml of ethyl acetate. The organic phases are combined and washed with water. The solvent is removed in vacuo and the oily residue is chromatographed on silica gel (mobile phase: methylene chloridelmethanol=100/1). This gives 0.34 g of the title compound of melting point 107° C. (diethyl ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06696461B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-81c653e2550948a39c9d0abcfd4ccad9 |
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| Source note | uspto-grants-2004_02 |
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