HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 5-(Acetylamino)methylimidazo[5,1-b]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 5-Aminomethylimidazo[5,1-b]thiazole | HCID 21262358 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(Acetylamino)methylimidazo[5,1-b]thiazole | HCID 22916699 | 83% |
Reaction Steps
To a solution of 150 mg (0.98 mmol) of 5-aminomethylimidazo[5,1-b]thiazole in 1 ml of methylene chloride were added 1 ml of acetic anhydride and 0.5 ml of pyridine, and the mixture was stirred overnight at room temperature. The reaction solution was concentrated. The residue was dissolved in methylene chloride, and washed with water. The organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by flash column chromatography using silica gel, eluting with ethyl acetate to give 159 mg (yield 83%) of the title compound as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05663162 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-e108199616c24ebc956c7e61c3bed672 |
| Source note | uspto-grants-1997_09 |