HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → Aripiprazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-(4-Chlorobutoxy)-1,2,3,4-tetrahydroquinolin-2-one | HCID 10467467 | — |
| Reactant | 1-(2,3-Dichlorophenyl)piperazine hydrochloride | HCID 11630372 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Aripiprazole | HCID 60795 | 159.6% |
Reaction Steps
A mixture of 100 gm 7-(4-chloro butoxy)-3,4-Dihydrocarbostyril in 600 ml acetonitrile with sodium iodide (88.6 gm), K2CO3 (109 gm), Tetrabutylammonium bromide (TBAB) (0.5 gm) and 1-(2,3-dichlorophenyl)piperazine hydrochloride (110 gm) was stirred at ambient temperature. The reaction mixture was refluxed and maintained at reflux until reaction completes. The reaction mass was cooled at room temperature. DM Water (500 ml) was added to reaction mass and stirred for 30 min at ambient temperature. The mass was filtered and washed with water till pH of filtrate came to 7.0-7.5. The solid was dried in hot air oven at 60° C. to give Aripiprazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07777039B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-07502c785a674e6b88dc91d2c05aded7 |
| Source note | uspto-grants-2010_08 |