HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876832Generated: October 30, 2026
Methyl iodide → Imidazo[1,2-a]pyridine-6-carbonitrile, 3-(methoxymethyl)-
https://huagongshe.com/reaction/876832
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(Hydroxymethyl)imidazo[1,2-a]pyridine-6-carbonitrile | HCID 67305931 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Imidazo[1,2-a]pyridine-6-carbonitrile, 3-(methoxymethyl)- | HCID 67305506 | — |
Reaction Steps
To a solution of 3-(hydroxymethyl)-imidazo[1,2-a]pyridine-6-carbonitrile (7-2) (346 mg, 2 mmol) in 20 mL of THF was added sodium hydride (240 mg, 60% in oil) at 0° C. The reaction mixture was stirred at 0° C. for 1 h, then methyl iodide (615 mg, 4.3 mmol) was added. The reaction was stirred at room temperature overnight. The mixture was treated with aqueous Na2CO3, then concentrated. The residue was diluted with water and extracted with EtOAc. The combined organics were dried over Na2SO4 and concentrated to afford the title compound (300 mg). MS (m/z): 188.0 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987269B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-64d87714e81746d1820b5922727f1ab6 |
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| Source note | uspto-grants-2015_03 |
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