HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 5-bromo-N,N,1-trimethyl-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,N-dimethyl-6-oxo-1,6-dihydropyridine-3-carboxamide | HCID 89781747 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 5-bromo-N,N,1-trimethyl-6-oxo-1,6-dihydropyridine-3-carboxamide | HCID 89783539 | — |
Reaction Steps
To a solution of 5-bromo-N,N-dimethyl-6-oxo-1,6-dihydropyridine-3-carboxamide (100 mg, 0.408 mmol) and iodomethane (57.9 mg, 0.408 mmol) in DMSO (3 mL) was added potassium carbonate (56.4 mg, 0.408 mmol). The mixture was stirred at room temperature overnight, filtered, and purified via preparative HPLC, eluting with a gradient of 10-90% ACN (containing 0.035% TFA) in H2O (containing 0.05% TFA). The product was dried under vacuum 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-ccb0f21f6b3842d49e620e2e70932de7 |
| Source note | uspto-grants-2016_09 |