Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | ethyl imidazo[1,2-a]pyridine-5-carboxylate | HCID 11127069 | — |
| Reactant | N,N-dimethylmethyleneammoniumiodide | HCID 21892197 | — |
| Product | HCID 53654791 | HCID 53654791 | — |
Reaction Steps
To a solution of 1.90 g (10.0 mmol) of 5-ethoxycarbonylimidazo[1,2-a]pyridine in 40 ml of acetonitrile was added 2.41 g (13.0 mmol) of N,N-dimethylmethyleneammonium iodide. The mixture was heated for two hours under reflux. The solvent was distilled off. To the residue was added methylene chloride. The mixture was washed with an aqueous solution of sodium thiosulfate and an aqueous solution of sodium hydrogencarbonate, successively, dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by column chromatography (eluent: ethyl acetate) to afford 1.496 g of the desired compound (60.6%, a pale yellow solid). This product was recrystallized from ethyl acetate to afford the desired compound (colorless crystals), m.p.117.0-118.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06251905B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-7d5e627c3c984e7cb08c3a5582e108a0 |
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| Source note | uspto-grants-2001_06 |
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