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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937730Generated: November 1, 2026

Hydrochloric Acid → (R)-1-(2-Methoxyphenyl)-4-[2-(methyl)-2-(2-pyridinylamino)ethyl]piperazine

https://huagongshe.com/reaction/1937730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-(2-Methoxyphenyl)piperazineHCID 1346—
Reactant(R)-4-methyl-3-pyridin-2-yl[1,2,3]oxathiazolidine-2,2-dioxideHCID 22863100—
SolventAcetonitrileHCID 6342—
Product(R)-1-(2-Methoxyphenyl)-4-[2-(methyl)-2-(2-pyridinylamino)ethyl]piperazineHCID 2527306279.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

9.16 grams (46.6 millimoles) of 1-(2-methoxyphenyl)piperazine in one portion was added under argon to a solution of 10 grams (46.6 millimoles) of (R)-4-methyl-3-pyridin-2-yl[1,2,3]oxathiazolidine-2,2-dioxide in 200 milliliters of acetonitrile. The mixture became yellow. After ½ hour, the reaction mixture was heated to 50° C. for 1 hour and then stirred at room temperature overnight Then dilute hydrochloric acid was added. The mixture was washed with ethyl acetate, basified to pH 12 and extracted twice with ethyl acetate. The organic phases were washed with brine, dried (Mg SO4) and subjected to evaporation to give 12.053 grams of the title compound which was purified by columning in the system ethyl ether/hexane (1:1) Al2O3 to afford 9.96 grams of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06395902B1
Source datasetuspto-grants-2002_05
ORD IDord-e26cd414d59c44b5b82b84b3bff0d63f
Source noteuspto-grants-2002_05