Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-[3-(Hydroxy)propylthio]imidazo[1,2-a]pyridine | HCID 23362890 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23362919 | HCID 23362919 | 35.9% |
Reaction Steps
To a solution of 5-[3-(hydroxy)propylthio]imidazo[1,2-a]pyridine (803 mg, 3.86 mmoles) in tetrahydrofuran (30 ml) was added 60% sodium hydride in oil (0.19 g, 4.6 mmoles) with stirring under ice-cooling and the mixture was further stirred under ice-cooling for 30 minutes. To the reaction mixture was added methyl iodide (0.36 ml, 5.8 mmoles), followed by stirring at room temperature overnight. The reaction mixture was poured into water, which was extracted with methylene chloride (30 ml×3). The methylene chloride layers were combined and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography (eluent:ethyl acetate) to obtain 308 mg of the desired product (35.9%, light brown oily product).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05587383 |
|---|
| Source dataset | uspto-grants-1996_12 |
|---|
| ORD ID | ord-17083d6b5c3041e3a38c3e146cabe642 |
|---|
| Source note | uspto-grants-1996_12 |
|---|