Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-[3-(Hydroxy)propylthio]imidazo[1,2-a]pyridine | HCID 23362890 | — |
| Reactant | HCID 178418629 | HCID 178418629 | — |
| Product | HCID 23362844 | HCID 23362844 | 58.9% |
Reaction Steps
To a solution of 5-[3-(hydroxy)propylthio]imidazo[1,2-a]pyridine (1.070 g, 5.137 mmoles) in tetrahydrofuran (30 ml) was added 60% sodium hydride in oil (0.25 g, 6.2 mmoles) with stirring under ice-cooling and the mixture was stirred under ice-cooling for 30 minutes. To the reaction mixture was added methyl iodie (1.53 g, 7.71 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 0.987 g of the desired compound (58.9%, light brown oily product).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05244908 |
|---|
| Source dataset | uspto-grants-1993_09 |
|---|
| ORD ID | ord-f9658666c16f4e2d9c1027809e78ff12 |
|---|
| Source note | uspto-grants-1993_09 |
|---|