HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 5-(N-Methylamino)methylimidazo[5,1-b]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-(N-methyl-N-trifluoroacetylamino)methylimidazo[5,1-b]thiazole | HCID 22916700 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-(N-Methylamino)methylimidazo[5,1-b]thiazole | HCID 21262403 | 109.2% |
Reaction Steps
To a solution of 394 mg (1.49 mmol) of the above-obtained 5-(N-methyl-N-trifluoroacetylamino)methylimidazo[5,1-b]thiazole in 3 ml of methanol was added 3 ml of a 10% aqueous solution of sodium hydroxide, and the mixture was stirred at room temperature for 1 hour. The methanol was distilled off under reduced pressure. The resultant was extracted three times with chloroform. The organic layer was dried over anhydrous potassium carbonate, and concentrated under reduced pressure to give 272 mg of the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05663162 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-b23bb46eae8742218a636a1c5b8af5e5 |
| Source note | uspto-grants-1997_09 |