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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864365Generated: October 30, 2026

1-(2,5-Xylyl)piperazine → HCID 67141139, compound

https://huagongshe.com/reaction/1864365

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2,5-Xylyl)piperazineHCID 70542—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantPotassium bisulfateHCID 516920—
ReactantHCID 10955823HCID 10955823—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 67141139HCID 6714113970.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

(RS)-2-benzenesulfonylamino-3-hydroxy-propionic acid (1.204 g) was dissolved in tetrahydrofuran (15 ml) and cooled to 0° C. 1-(2,5-Dimethylphenyl)-piperazine (1.12 g), (benzotriazol-1-yloxy)-tris-(dimethylamino)-phosphonium-hexafluorophosphate (BOP reagent, 3.26 g) and N-ethyl-diisopropylamine (1.90 g) were added. The mixture was stirred at room temperature for 18 h. Ethyl acetate and a 10% KHSO4 solution were added. The organic phase was washed with water, dried, filtered and evaporated. The product was purified by chromatography (SiO2, cyclohexane/ethyl acetate 1:1=>ethyl acetate) to give (RS)—N-{2-[4-(2,5-dimethyl-phenyl)-piperazin-1-yl]-1-hydroxymethyl-2-oxo-ethyl}-benzenesulfonamide (1.45 g) as a colorless foam. MS: 418.3 ([M+H]+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625902B2
Source datasetuspto-grants-2009_12
ORD IDord-995bdd049fec4548b55de229e263bed1
Source noteuspto-grants-2009_12