HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 18979095, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 18979069 | HCID 18979069 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 18979095 | HCID 18979095 | — |
Reaction Steps
5-Bromo-2-t-butyloxycarbonylamino-8-Methoxyquinoline (1.21 g) and tetrahydrofuran (20 ml) were combined at room temperature under a nitrogen atmosphere. Sodium hydride (60% dispersion in oil) (164 mg) was added and the reaction mixture stirred for 2 h whilst effervescence occurred and a yellow colour appeared. Iodomethane (0.43 ml) was then added and stirring was continued for 2 h after which time the reaction was diluted with ethyl acetate (100 ml), washed successively with water, saturated aqueous sodium bicarbonate and brine, then dried (magnesium sulphate) and evaporated in vacuo to give the title compound (1.1 g) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05804588 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-8da48e0f22ce4333aa4ab2cfb937ba4a |
| Source note | uspto-grants-1998_09 |