HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → 8-Amino-2-methylimidazo[1,2-a]pyridine-6-carboxamide mesylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5,6-Diaminonicotinamide | HCID 9942190 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 8-Amino-2-methylimidazo[1,2-a]pyridine-6-carboxamide mesylate | HCID 18357440 | 33.3% |
Reaction Steps
5,6-diaminonicotinamide (10 g, 66 mmol), chloroacetone (6.1 g, 66 mmol) and sodium bicarbonate (11.2 g, 132 mmol) were added to dimethylformamide (200 ml) and the mixture was stirred for 72 h. at room temperature. Most of the solvent was evaporated under reduced pressure and methanesulfonic acid (6 g, 63 mmol) was added. More solvent was evaporated under reduced pressure and ethanol was added to the residue. Upon warming the mixture to 60° C. the product crysstallized as salt and was filtred off to give 6 g (32%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06313137B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-1ec0dec5b00a49c4b9ce5e4972b6cd1a |
| Source note | uspto-grants-2001_11 |