HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tacrine → 1,2,3,4-Tetrahydroacridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tacrine | HCID 1935 | — |
| Reactant | 4-Bromobutyryl chloride | HCID 70225 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,2,3,4-Tetrahydroacridine | HCID 155315 | — |
Reaction Steps
To a solution of tacrine (4 g, 20.17 mmoles) in chloroform (50 ml) and N,N-dimethylformamide (15 ml), 4-bromobutyroylchloride (3.5 ml, 30.25 mmoles) is added. The reaction mixture is maintained under stirring at room temperature for 6 hours and then diluted with chloroform and washed with water. The organic phase, anhydrified with sodium sulphate, is evaporated at reduced pressure. The crude product is purged by chromatography on silica gel, eluting with n-hexane/ethyl acetate 8/2 (ratio by volume). 9-[4-bromo)butyroylamino]-1,2,3,4-tetrahydroacridine is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07399878B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-7cb704a7b3024394a2e669e1c73a362d |
| Source note | uspto-grants-2008_07 |