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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566590Generated: November 2, 2026

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

https://huagongshe.com/reaction/566590

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 millilitres 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 numberUS06175012B1
Source datasetuspto-grants-2001_01
ORD IDord-218d6a16b8464257ab4e0adf70060ea1
Source noteuspto-grants-2001_01