HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 6-Chloro-3-(piperazin-1-yl)benzo[d]isoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3,6-Dichlorobenzo[d]isoxazole | HCID 13568449 | — |
| Product | 6-Chloro-3-(piperazin-1-yl)benzo[d]isoxazole | HCID 13568451 | 71.1% |
Reaction Steps
3,6-dichlorobenzisoxazole (5.2 g, 27.8 mmol), and anhydrous piperazine (24 g, 278 mmol) are placed in an egg type flask and react at 120° C. for 24 hours. After completion of the reaction, 52 ml of an ice-water mixture is added for quenching the reaction. Further 15 ml of 50% NaOH solution is added to the reaction solution. The reaction solution is stirred for 5 minutes and extracted with dichloromethane (30 ml×3). The dichloromethane layer is combined, washed with 20 ml of saturated saline, dried over anhydrous MgSO4, evaporated to dryness, and subjected to a separation on a column of alumina (200-300 mesh), eluting with dichloromethane:methanol-100:1, to obtain 4.7 g of 6-chloro-3-piperazinyl-benzisoxazole, with a yield of 71%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08653069B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-736d716173fd49f089f5651ed616c9c1 |
| Source note | uspto-grants-2014_02 |