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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Methoxyphenyl)piperazineHCID 1346—
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 10332575HCID 10332575—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 19752298HCID 1975229853.2%

Reaction Conditions

Temperature180 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05225412
Source datasetuspto-grants-1993_07
ORD IDord-153a2aefdb9a4a4c9e4b76f1cddd3331
Source noteuspto-grants-1993_07