HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 3-iodo-7-methoxy-1-methyl-1H-pyrrolo[2,3-c]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Iodo-7-methoxy-1H-pyrrolo[2,3-c]pyridine | HCID 53412719 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-iodo-7-methoxy-1-methyl-1H-pyrrolo[2,3-c]pyridine | HCID 90387813 | 95% |
Reaction Steps
3-Iodo-7-methoxy-1H-pyrrolo[2,3-c]pyridine (0.75 g, 2.74 mmol) in dimethylformamide (10 mL) was treated with 60% sodium hydride in mineral oil (0.219 g, 5.47 mmol) at room temperature for 20 minutes. To this solution was added methyl iodide (0.505 g, 3.56 mmol). The reaction mixture was stirred for 3 hours at room temperature. The reaction mixture was partitioned between water and ethyl acetate. The aqueous layer was extracted three times with ethyl acetate. The combined organic layers were washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated. The residue was purified by flash column chromatography (silica gel, 10% ethyl acetate/hexanes to give 0.75 g (95%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321764B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-1dd57418a9094f3e8ee3a63fc3515d58 |
| Source note | uspto-grants-2016_04 |