HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 23362878, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-[3-(Hydroxy)propylthio]imidazo[1,2-a]pyridine | HCID 23362890 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23362878 | HCID 23362878 | 100% |
Reaction Steps
To a solution of 5-[3-(hydroxy)propylthio]imidazo[1,2-a]pyridine (2.00 g, 9.60 mmoles) and triethylamine (1.60 ml, 11.5 mmoles) in methylene chloride (50 ml) was added acetic anhydride (1.10 ml, 11.6 mmoles) with stirring at room temperature and the mixture was further stirred at room temperature for 7.5 hours. The reaction mixture was washed with an aqueous 1N sodium hydroxide solution and dried. After the solvent was distilled off, the residue was purified by column chromatography [eluent: hexane/acetone (1:1)] to obtain 2.40 g of the desired product (100%, brown oily product).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05244908 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-d9e2fcc0263e44d98d5c9394e962dbc0 |
| Source note | uspto-grants-1993_09 |