HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-(Hydroxyaminocarbonyl)methylimidazo[5,1-b]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 3-Ethoxycarbonylmethylimidazo[5,1-b]thiazole | HCID 19605065 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(Hydroxyaminocarbonyl)methylimidazo[5,1-b]thiazole | HCID 19605027 | 73.1% |
Reaction Steps
To 2 ml of an ethanol solution containing 204.3 mg of 3-ethoxycarbonylmethylimidazo[5,1-b]thiazole, 108.2 mg of hydroxylamine hydrochloride and 210.2 mg of a sodium ethoxide powder were added, and the mixture was then stirred at room temperature for 2 hours. Under ice-cooling, 0.4 ml of 1N hydrochloric acid was added to the reaction solution to neutralize the solution. The solvent was evaporated under reduced pressure, and the resulting residue was purified by Diaion HP-20 Resin to obtain 140 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05990101 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-e4a0e5b1563f4d25a1527d34a8765996 |
| Source note | uspto-grants-1999_11 |