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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 330393Erstellt: 24. Oktober 2026

Triethylamine → N-[2-(Phenylsulfonyl)ethyl]-1-piperidineethanamine maleate

https://huagongshe.com/reaction/330393

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt((2-Chloroethyl)sulphonyl)benzeneHCID 13646—
EduktN-(2-Aminoethyl)piperidineHCID 33944—
EduktMaleic AcidHCID 444266—
LösungsmittelMethanolHCID 887—
LösungsmittelAcetonitrileHCID 6342—
ProduktN-[2-(Phenylsulfonyl)ethyl]-1-piperidineethanamine maleateHCID 7036054360,78%

Reaktionsschritte

A mixture of 40.94 g (0.20 mole) of [(2-chloroethyl)sulfonyl]benzene, 27.85 g (0.217 mole) of N-(2-aminoethyl)piperidine and 28.0 g (0.277 mole) of triethylamine in 800 ml of acetonitrile was stirred at room temperature overnight. The solvent was removed in vacuo, and the residue was partitioned between methylene chloride and dilute sodium hydroxide. The methylene chloride solution was dried over magnesium sulfate, and the solvent was removed in vacuo. The residue was dissolved in methanol, a solution of 2 equivalents of maleic acid in methanol was added, and the product crystallized from the solution at room temperatue to give 64.35 g (60.78%) of title compound as a white crystalline solid, mp 154°-155.5° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04895840
Quelldatensatzuspto-grants-1990_01
ORD IDord-02a04086823f4a4e8450854c0a958793
Quellennotizuspto-grants-1990_01