HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 5-bromo-N-(2-hydroxyethyl)-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-bromo-N-(2-hydroxyethyl)-6-oxo-1,6-dihydropyridine-3-carboxamide | HCID 89781750 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 5-bromo-N-(2-hydroxyethyl)-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide | HCID 89794782 | — |
Reaction Steps
A mixture of 5-bromo-N-(2-hydroxyethyl)-6-oxo-1,6-dihydropyridine-3-carboxamide (400 mg, 1.532 mmol), iodomethane (0.114 mL, 1.839 mmol), and potassium carbonate (212 mg, 1.532 mmol) in DMSO (5 mL) was stirred at room temperature overnight. The reaction mixture was subsequently filtered and purified via preparative HPLC, eluting with a gradient of 1-30% ACN in H2O (containing 10 mM NH4HCO3) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09434743B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-f7b48de156a34586a0e3a1ae6d251c59 |
| Source note | uspto-grants-2016_09 |