HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483432Generated: October 30, 2026
1-(2-Methoxyphenyl)piperazine → HCID 19752298, compound
https://huagongshe.com/reaction/483432
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(2-Methoxyphenyl)piperazine | HCID 1346 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 10332575 | HCID 10332575 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 19752298 | HCID 19752298 | 53.2% |
Reaction Steps
A mixture of N-(3-chloropropyl)-1,2-benzisothiazole-3-carboxamide (4.2 g), 1-(2-methoxyphenyl)piperazine (3.3 g), potassium carbonate (4.55 g), and sodium iodide (100 mg) in dry N-methylpyrrolidinone (150 ml) was heated to 180° C., with stirring, under nitrogen. After 24 hr, the reaction mixture was allowed to cool to room temperature and partitioned between ether/water. The organic phase was dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated in vacuo. The residue was chromatographed on silica using ether as the eluent. The appropriate fractions were collected and evaporated. The residue was taken up in ether and hydrogen chloride in ether was added. Recrystallization of the precipitate from methanol/dichloromethane/ether provided 2.12 g (26.6%) of product, mp 191°-194° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05225412 |
|---|
| Source dataset | uspto-grants-1993_07 |
|---|
| ORD ID | ord-153a2aefdb9a4a4c9e4b76f1cddd3331 |
|---|
| Source note | uspto-grants-1993_07 |
|---|