HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chloro-2,4-pentanedione → 3-Acetyl-7-chloro-2-methylimidazo[2,1-a]isoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chloro-2,4-pentanedione | HCID 74328 | — |
| Reactant | 5-Chloroisoquinolin-1-amine | HCID 13821825 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-Acetyl-7-chloro-2-methylimidazo[2,1-a]isoquinoline | HCID 20142437 | 9% |
Reaction Steps
To a suspension of 1-amino-5-chloroisoquinoline (10 g) in chloroform (150 ml) was added dropwise 3-chloro-2,4-pentanedione (11.3 g). The mixture was refluxed for 6 hours and then allowed to stand at room temperature over night. The mixture was washed successively with aqueous sodium bicarbonate and water, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography on silica gel (200 g) with chloroform as an eluent to afford a solid. This solid was recrystallized from ethyl acetate to give 3-acetyl-7-chloro-2-methylimidazo[2,1-a]isoquinoline (1.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04686227 |
| Source dataset | uspto-grants-1987_08 |
| ORD ID | ord-ede232d689f540df962a4f077637f4cb |
| Source note | uspto-grants-1987_08 |